We, Middle East Testing Services (METS Laboratory) are the leaders in laboratory testing and recognized as the best testing lab. We are ISO 17025 accredited in all streams of lab testing. We ensure your test requirements are met with the highest level of service and highest quality results in a timely fashion at a reasonable cost.
Thinking we are in UAE, but distance is not a barrier. Anywhere you are we will reach you. We value every opportunity to serve you.
Any laboratory testing including the one below, we are there as your trusted testing partner. We are expertise in all SASO product testing
Cosmetics Testing
Textile Testing
Footwear Testing
Leather Testing
Food Testing
Paint testing
Fire Propagation Testing
Sound Transmission Loss
Halal Testing
Polymer Analysis
Electrical Testing
ROHS testing
CDPH Testing
Virology Testing
Tobacco Testing
Migration Testing
Nutritional Labelling
Coal & Crude Oil Testing
Toys Testing
Microplastics Testing
Recyclable Plastics
Biocompatibility Testing
Failure Analysis
Dermatology Testing
SEM Studies
Our technical team is ready for all your queries. We are just a right click away from you.
In the wake of the COVID-19 pandemic, hand sanitizers have become an essential part of daily life, playing a crucial role in maintaining public health and hygiene. However, the effectiveness of a hand sanitizer is not just about its alcohol content; it also involves ensuring that the product meets stringent safety and efficacy standards. This is where sanitizer testing labs come into play. These labs are responsible for evaluating the quality, safety, and effectiveness of sanitizers through a series of rigorous procedures. In this blog, we will explore the key procedures carried out in a Sanitizer Testing Laband why they are vital for public safety.
Alcohol Content Verification
One of the most critical procedures in a sanitizer testing lab is the verification of alcohol content. The effectiveness of a hand sanitizer largely depends on its alcohol concentration, which needs to be within a specific range to effectively kill germs and viruses. Testing should be following United States Pharmacopeia (USP), Federal Chemical Codex (FCC) and other national regulatory guidelines including GSO, SASO .
Sanitizer testing labs use advanced analytical techniques, such as gas chromatography, to accurately measure the alcohol content in sanitizer formulations. This verification ensures that the product meets the required standards and is capable of providing the necessary protection against pathogens by verifying the percentage of ethanol, methanol, n-propanol and iso-propanol.
Microbial Efficacy Testing
Microbial efficacy testing is another crucial procedure in a sanitizer testing lab. This process evaluates the sanitizer’s ability to eliminate a wide range of microorganisms, including bacteria, viruses, and fungi. The goal is to ensure that the sanitizer not only contains the right ingredients but is also effective in real-world conditions.
During microbial efficacy testing, the sanitizer is exposed to various strains of microorganisms in a controlled environment. The lab then measures the reduction in the number of viable microorganisms after exposure to the sanitizer.
Skin Irritation and Sensitization Testing
While hand sanitizers are essential for hygiene, they are also in direct contact with the skin, making it important to ensure they do not cause irritation or allergic reactions. Sanitizer testing labs conduct skin irritation and sensitization testing to evaluate the product’s safety for regular use.
In these tests, the sanitizer is applied to skin models or human volunteers under controlled conditions. The lab monitors any signs of irritation, redness, or allergic reactions over a specified period. If the sanitizer causes significant skin irritation or sensitization, it may require reformulation to make it safer for consumers.
Stability and Shelf Life Testing
Stability testing is essential for determining the shelf life of a hand sanitizer. Sanitizer testing labs evaluate how the product’s formulation holds up over time when exposed to various environmental conditions, such as temperature changes, light exposure, and humidity.
During stability testing, the sanitizer is stored under different conditions for an extended period, and its physical and chemical properties are periodically tested. The lab assesses whether the sanitizer maintains its alcohol content, effectiveness, and safety throughout its intended shelf life.
Conclusion
Sanitizer testing labs play an essential role in ensuring the safety, effectiveness, and quality of hand sanitizers. Through a series of rigorous procedures, including alcohol content verification, microbial efficacy testing, skin irritation testing, stability testing, residue testing, and toxicology assessments, these labs provide the necessary validation that a hand sanitizer can deliver on its promises. As hand sanitizers continue to be a crucial tool in maintaining public health, the work of sanitizer testing labs is more important than ever. For manufacturers, investing in thorough testing not only ensures compliance with regulatory standards but also builds consumer trust and confidence in their products.
As the furniture industry continues to evolve, with consumers demanding higher standards for quality and safety, furniture testing has become increasingly essential. Furniture Testing Lab play a critical role in ensuring that products meet safety regulations and perform as expected. In this blog, we’ll explore why furniture testing is crucial and how it contributes to delivering reliable and safe products to consumers.
Ensuring Compliance with Safety Standards
One of the primary reasons furniture testing is vital is its role in ensuring compliance with safety standards. Regulatory bodies such as the American National Standards Institute (ANSI), the International Organization for Standardization (ISO), and other national authorities have established guidelines for furniture safety. These standards are designed to protect consumers from potential hazards associated with furniture use, such as structural failures or toxic materials.
Furniture testing labs are responsible for evaluating furniture products to ensure they meet these regulatory requirements. Through rigorous testing procedures, these labs help manufacturers avoid using unsafe materials and designs, ensuring that their products can be safely marketed and used. Compliance with these standards not only protects consumers but also enhances the reputation and success of furniture brands.
Identification and Quantification of Hazardous Materials
Another crucial function of furniture testing labs is the identification and quantification of hazardous materials in furniture products. Certain materials, when used inappropriately or in high concentrations, can pose health risks, such as exposure to toxic chemicals or harmful VOCs (Volatile Organic Compounds).
These labs analyze the materials used in furniture construction to ensure they meet safety standards and do not contain harmful substances. By identifying and quantifying these materials, furniture testing labs help prevent unsafe products from reaching consumers, thereby safeguarding public health.
Testing for Product Durability and Performance
Furniture testing labs also play a significant role in assessing the durability and performance of furniture products. Durability testing involves subjecting furniture to various stress conditions, such as weight loads, impacts, and environmental factors, to observe how it performs over time. This testing helps determine whether a product will maintain its integrity and functionality throughout its intended lifespan.
During performance testing, labs analyze factors such as resistance to wear and tear, stability, and overall structural soundness. This ensures that the furniture meets consumer expectations for quality and longevity.
Safety Assessment of New Materials and Designs
Innovation in the furniture industry often involves the use of new materials and designs that promise enhanced aesthetics, comfort, or functionality. Furniture testing labs are responsible for conducting safety assessments of these new elements. They perform a range of tests to evaluate the potential risks associated with new materials and design features.
These assessments might include testing for chemical emissions, flammability, and mechanical stability. By thoroughly evaluating these aspects, furniture testing labs help ensure that new products are safe and reliable before they enter the market.
Conclusion
Furniture testing labs are indispensable to the furniture industry, playing a vital role in ensuring the safety, quality, and performance of furniture products. From regulatory compliance and hazardous material identification to durability testing and new material assessments, these labs provide the expertise and assurance that furniture products meet the highest safety standards.
The global cosmetics industry is booming, with consumers becoming increasingly aware of the ingredients in the products they use daily. As this awareness grows, so does the importance of ensuring that cosmetic products are safe for human use. Chemicals Testing Labs play a pivotal role in this process by rigorously testing cosmetic products to ensure they are free from harmful substances and safe for consumer use. In this blog, we’ll explore why chemicals testing labs are essential for the safety of cosmetic products and how they contribute to maintaining the integrity of the beauty industry.
Ensuring Compliance with Regulatory Standards
One of the primary reasons for chemicals testing labs is to ensure the safety of the cosmetic product in compliance with regulatory standards. Regulatory bodies like the U.S. Food and Drug Administration (USFDA), the European Medicines Agency (EMA), ANAB (NSF/ANSI 455-3-2018) and other national authorities SFDA, EU directive, SASO, GSO, QGOSM, QS 1943, QS 1046:2018 have strict guidelines regarding the ingredients that can be used in cosmetic products.
Chemicals testing labs are responsible for analyzing the ingredients used in cosmetic formulations to ensure they meet these regulatory requirements. By conducting detailed chemical analyses, these labs help manufacturers avoid the use of banned or restricted substances, ensuring that their products can be safely marketed and sold. For example, UNBS and KEBS banned more than hundreds of cosmetic brands from the marked due to their alleged contamination with mercury and hydroquinone.
Identification and Quantification of Harmful Substances
Another critical function of chemicals testing labs is the identification and quantification of harmful substances in cosmetic products. Certain chemicals, when present in high concentrations or when used inappropriately, can cause skin irritation, allergic reactions, or even long-term health issues.
These labs also measure the concentration of each ingredient to ensure it falls within safe and permissible limits. By identifying and quantifying these substances, chemicals testing labs help prevent harmful products from reaching consumers, thus safeguarding public health. For example, as per QS 1943, formaldehyde content is prohibited in hair shampoo or any hair products containing keratin as well as the limit of 1.4- Dioxane does not exceed 10ppm in hair shampoo, the usage of PPD (para phenylenediamine) is restricted to less than 6% while prohibited in black henna and eyebrows/eyelashes dye respectively.
Testing for Product Stability and Shelf Life
Chemicals testing labs also play a crucial role in determining the stability and shelf life of cosmetic products. Stability testing involves subjecting products to various environmental conditions, such as temperature, humidity, and light exposure, to observe how they react over time. This testing helps determine whether a product will remain safe and effective throughout its intended shelf life.
During stability testing, chemicals testing labs analyze whether any chemical changes occur that could compromise the product’s safety or effectiveness. For example, certain ingredients might degrade over time, leading to the formation of harmful byproducts. So, the incorporation of preservatives is vital to enhance the shelf life and stability of the products. Thus, preservation testing is crucial along with product stability and shelf life to determine the effectiveness of preservatives used in cosmetic products. ASTM E640 standard is commonly used for preservation testing, assessing the antimicrobial properties of cosmetic formulations.
Safety Assessment of New Ingredients
Innovation in the cosmetics industry often involves the introduction of new ingredients that promise enhanced benefits, such as anti-aging effects, improved hydration, or better sun protection.
Chemicals testing labs are responsible for conducting these safety assessments. They perform a battery of tests to evaluate the potential toxicity, irritancy, and allergenicity of new ingredients. These tests might include in vitro studies, skin sensitization tests, and other evaluations designed to predict how the ingredient will interact with human skin.
Conclusion
Chemicals testing labs are indispensable to the cosmetics industry, playing a vital role in ensuring the safety and quality of cosmetic products. From regulatory compliance and harmful substance identification to stability testing and new ingredient safety assessments, these labs provide the expertise and assurance that cosmetic products meet the highest safety standards. In an industry where consumer trust is paramount, the role of chemicals testing labs in safeguarding public health and maintaining brand integrity cannot be overstated. For any cosmetic company, partnering with a reputable chemical testing lab is essential to delivering safe, effective, and high-quality products to the market.
Microbiological testing plays a vital role in ensuring the safety, quality, and compliance of various products, especially in industries such as food and beverage, pharmaceuticals, cosmetics, and environmental monitoring. A Microbiological Testing Lab serves as a critical checkpoint where products are scrutinized for microbial contamination and other potential hazards that could pose risks to public health. Understanding the key functions of a microbiological testing lab can help businesses ensure their products meet the highest standards of safety and quality.
Detection of Pathogens and Contaminants
One of the primary functions of a microbiological testing lab is the detection of pathogens and contaminants. These labs use sophisticated methods to identify harmful microorganisms such as bacteria, viruses, fungi, and parasites that could cause disease if consumed or used. For instance, in the food industry, microbiological testing is essential to prevent outbreaks of foodborne illnesses caused by pathogens like Salmonella, E. coli, and Listeria. By detecting these contaminants early in the production process, companies can take corrective actions to ensure their products are safe for consumption.
Quality Control and Assurance
Microbiological testing labs play a crucial role in the quality control and assurance processes of various industries. These labs help ensure that products meet regulatory standards and industry benchmarks for microbial content. For example, in the pharmaceutical industry, drugs and medical devices must undergo rigorous microbiological testing to confirm their sterility and absence of harmful microbes. This testing ensures that the final products are not only effective but also safe for patient use. Quality control through microbiological testing helps prevent costly recalls and protects companies from legal liabilities.
Environmental Monitoring
Environmental monitoring is another key function of microbiological testing labs. These labs assess the microbial levels in various environments, such as manufacturing facilities, hospitals, and water treatment plants. Monitoring the microbial load in these environments is essential to prevent contamination of products and ensure compliance with health and safety regulations. For instance, in cleanroom environments, microbiological testing is conducted to verify that the air, surfaces, and equipment are free from harmful microorganisms. This monitoring helps maintain the integrity of the production process and ensures that products are manufactured in a sterile environment.
Method Development and Validation
Microbiological testing labs are also involved in the development and validation of testing methods. These labs design and refine testing protocols to accurately detect and quantify microorganisms in various products and environments. Method validation is a critical step that ensures the reliability and accuracy of testing results. By developing robust testing methods, microbiological testing labs contribute to the continuous improvement of quality control processes in industries such as food and pharmaceuticals. Moreover, validated methods are essential for regulatory compliance, as they demonstrate that testing procedures are scientifically sound and produce consistent results.
Conclusion
Microbiological testing lab perform a wide range of critical functions that are essential for ensuring the safety, quality, and compliance of products across various industries. From detecting pathogens to validating testing methods and conducting environmental monitoring, these labs play a vital role in protecting public health and maintaining industry standards. As industries continue to evolve, the importance of microbiological testing labs will only increase, making them indispensable partners in the quest for product safety and excellence. Whether you are in the food, pharmaceutical, or environmental sector, partnering with a reliable microbiological testing lab is key to achieving success in today’s competitive market.
Water is essential for life, and its quality directly impacts our health and well-being. Whether it’s the water you drink, cook with, or bathe in, ensuring its safety is crucial. In this comprehensive guide, we’ll delve into the importance of water quality, the common contaminants found in water, and the various methods available for testing water quality.
Understanding Water Quality
Water quality refers to the chemical, physical, biological, and radiological characteristics of water. It determines the suitability of water for various uses, such as drinking, bathing, and irrigation. Poor water quality can lead to severe health issues, including gastrointestinal illnesses, reproductive problems, and neurological disorders.
Health Implications: Contaminated water can carry harmful pathogens and toxins that can cause diseases.
Environmental Impact: Polluted water can damage ecosystems, harming wildlife and disrupting natural processes.
Regulatory Requirements: Governments and organizations have established standards to ensure water safety. Regular testing helps in complying with these regulations and maintaining safe water supplies.
Types of Water Sources
Understanding the type of water source is crucial as different sources have varied contamination risks.
Tap Water: Supplied by municipal sources, usually treated to meet safety standards but can still pick up contaminants from pipes.
Well Water: Drawn from underground sources and may be susceptible to contamination from natural and human activities.
Surface Water: Includes lakes, rivers, and streams; more exposed to pollutants from runoff and industrial discharges.
Bottled Water: Generally considered safe, but not immune to quality issues. Always check for regulatory compliance.
Common Water Contaminants
Water can be contaminated by various substances:
Microbiological: Bacteria (e.g., E. coli), viruses, and protozoa.
Chemical: Lead, pesticides, nitrates, and heavy metals.
Physical: Sediments and particulates that affect water clarity.
Radiological: Radon and uranium, which can be naturally occurring or due to human activities.
Methods of Water Quality Testing
There are several ways to test water quality, each with its advantages and limitations:
Home Testing Kits
Types: Test strips, digital testers, and color disk kits.
How to Use: Typically involve collecting a water sample, applying the test medium, and comparing results to a color chart or digital readout.
Pros: Convenient and cost-effective for basic testing.
Cons: Limited accuracy and scope.
Laboratory Testing
Process: Involves sending a water sample to a certified lab for comprehensive analysis.
Benefits: Provides detailed and accurate results, identifying a wide range of contaminants.
Cons: More expensive and time-consuming.
On-site Professional Testing
When to Consider: Useful for complex water systems or when contamination is suspected.
Pros: Expert assessment and immediate recommendations.
Cons: Higher cost compared to home kits and laboratory testing.
Interpreting Test Results
Understanding water test results is essential for taking appropriate action:
Parameters and Units: Familiarize yourself with common parameters like pH, turbidity, and contaminant levels, usually measured in parts per million (ppm) or micrograms per liter (µg/L).
Standards: Compare results to guidelines set by regulatory bodies like the EPA and WHO.
Common Issues: Identify issues such as high levels of lead (indicating pipe corrosion) or coliform bacteria (suggesting fecal contamination).
Solutions for Contaminated Water
If tests reveal contaminants, several solutions are available:
Filtration Systems
Types: Activated carbon filters (remove chlorine, organic compounds), reverse osmosis systems (remove a wide range of contaminants), and UV purifiers (kill microorganisms).
Choosing the Right One: Based on specific contaminants and usage requirements.
Boiling and Chemical Treatments
Effective for killing bacteria and viruses but not suitable for chemical contaminants.
Point-of-Use vs. Point-of-Entry Solutions
Point-of-Use: Treat water at the tap, suitable for drinking and cooking.
Point-of-Entry: Treat water entering the home, providing comprehensive protection.
Regular Monitoring and Maintenance
Maintaining water quality requires regular testing and system upkeep:
Testing Frequency: At least once a year for well water; municipal water users should test every few years or if water quality changes.
Seasonal Factors: Test more frequently during high rainfall or drought conditions.
System Maintenance: Regularly check and replace filters, and ensure treatment systems are functioning correctly.
DIY vs. Professional Testing
Choosing between DIY and professional testing depends on several factors:
Pros and Cons
DIY: Cost-effective, convenient, but limited in scope.
Professional: More accurate and comprehensive, but higher cost.
Cost Considerations: Weigh the cost of testing against the potential health risks.
When to Opt for Professional Testing: If contamination is suspected, if you have a private well, or if previous tests have shown issues.
Conclusion
Ensuring safe and clean water is essential for health and well-being. Regular water quality testing, understanding test results, and taking appropriate action are critical steps in maintaining water safety. Don’t wait—get your water tested today and take proactive measures to protect yourself and your loved ones.
FAQs
What is the best method for testing water quality at home?
Home testing kits are convenient for basic tests, but for comprehensive analysis, laboratory testing is recommended.
How often should I test my water?
Test well water at least once a year. Municipal water users should test every few years or when water quality changes.
What contaminants should I test for in my water?
Common contaminants include bacteria, lead, nitrates, pesticides, and heavy metals. Test based on your water source and local issues.
How can I improve my water quality if contaminants are found?
Use filtration systems like activated carbon or reverse osmosis, boil water, or use chemical treatments depending on the contaminant type.
When should I consider professional water testing?
Opt for professional testing if you suspect contamination, have a private well, or if previous tests show issues.
The Public Works Authority, known as ASHGAL, is a key player in Qatar’s infrastructure development. ASHGAL has been at the forefront of promoting road safety through innovative strategies and comprehensive planning. This blog explores ASHGAL’s approach to road safety, highlighting the key initiatives and measures that are making Qatar’s roads safer for everyone.
Comprehensive Road Safety Strategy
ASHGAL’s approach to road safety is grounded in a comprehensive strategy that addresses various aspects of road design, construction, and maintenance. The authority’s strategy is designed to minimize accidents, enhance road user behavior, and ensure the safety of all road users.
Road Design and Infrastructure: ASHGAL ensures that road designs comply with international safety standards. This includes implementing features like proper signage, road markings, pedestrian crossings, and barriers to separate traffic flows.
Regular Maintenance: Continuous maintenance of road infrastructure is crucial. ASHGAL prioritizes regular inspection and repair of roads to prevent hazards such as potholes and worn-out markings.
Advanced Technology and Innovation
Incorporating advanced technology into road safety measures is a key aspect of ASHGAL’s approach. Leveraging technological advancements allows for more efficient monitoring and management of road safety.
Intelligent Traffic Systems (ITS): ASHGAL employs ITS to enhance traffic flow and safety. These systems include traffic cameras, sensors, and variable message signs that provide real-time information to road users.
Automated Speed Enforcement: The use of speed cameras and automated enforcement technologies helps in reducing speeding violations, which are a major cause of road accidents.
Public Awareness and Education
Educating the public about road safety is fundamental to ASHGAL’s approach. Awareness campaigns and educational programs are designed to inform and engage the community in road safety practices.
Safety Campaigns: ASHGAL conducts regular road safety campaigns to raise awareness about the importance of safe driving practices. These campaigns often focus on key issues such as speeding, seatbelt use, and the dangers of using mobile phones while driving.
School Programs: Education initiatives targeting young people are crucial. ASHGAL collaborates with schools to teach children about road safety from an early age, fostering a culture of safety that will carry into adulthood.
Collaboration with Stakeholders
Effective road safety management requires collaboration with various stakeholders. ASHGAL works closely with governmental bodies, private sector partners, and international organizations to enhance road safety measures.
Government Partnerships: Collaboration with the Ministry of Interior and traffic police ensures that road safety policies are effectively implemented and enforced.
International Cooperation:ASHGAL partners with international road safety organizations to stay updated on global best practices and integrate them into Qatar’s road safety strategy.
Conclusion
ASHGAL’s approach to road safety is multifaceted, combining advanced technology, public education, stakeholder collaboration, data analysis, and continuous infrastructure enhancement. These efforts are aimed at creating a safer road environment for all users. By understanding and supporting ASHGAL’s initiatives, we can contribute to making Qatar’s roads safer and reducing the number of traffic-related injuries and fatalities. The commitment of ASHGAL to road safety demonstrates the importance of a proactive and comprehensive strategy in achieving sustainable and effective road safety outcomes.
Quality Governance and Operational Safety Management (QGOSM) is a critical framework for ensuring safety and quality across various sectors. Keeping up with the latest updates in QGOSM is essential for organizations aiming to maintain high standards and regulatory compliance. This blog delves into the most recent developments in QGOSM that you should be aware of, highlighting how these updates can enhance your operational safety and quality management processes.
Introduction to QGOSM
QGOSM is designed to provide a structured approach to managing quality and safety within an organization. It encompasses a range of practices and procedures aimed at minimizing risks and ensuring consistent quality. The recent updates in QGOSM reflect the ongoing evolution of best practices and technological advancements in this field.
Integration of Advanced Technologies
One of the significant updates in QGOSM is the integration of advanced technologies to improve safety and quality management.
Artificial Intelligence (AI) and Machine Learning (ML): These technologies are being used to predict potential safety issues and quality defects before they occur. AI-driven analytics can process vast amounts of data to identify patterns and trends, enabling proactive measures.
Internet of Things (IoT): IoT devices are increasingly being used to monitor equipment and environmental conditions in real-time. This continuous monitoring helps in early detection of potential hazards, ensuring timely intervention.
Enhanced Risk Management Frameworks
The latest QGOSM updates emphasize the importance of robust risk management frameworks. These frameworks are designed to identify, assess, and mitigate risks more effectively.
Risk Assessment Tools: New tools have been introduced to enhance the accuracy and efficiency of risk assessments. These tools use data analytics to provide a comprehensive view of potential risks.
Continuous Improvement: The updates promote a culture of continuous improvement, where organizations regularly review and update their risk management practices to adapt to changing conditions and emerging threats.
Improved Regulatory Compliance
Staying compliant with regulations is a critical aspect of QGOSM. The latest updates provide clearer guidelines and enhanced support for regulatory compliance.
Compliance Management Systems: Advanced systems have been developed to help organizations stay compliant with local and international regulations. These systems offer automated tracking and reporting features to ensure all regulatory requirements are met.
Updated Standards and Protocols: New standards and protocols have been introduced to address contemporary challenges in safety and quality management. Organizations are encouraged to align their practices with these updated standards to maintain compliance and improve operational efficiency.
Conclusion
Keeping abreast of the latest updates in QGOSM is essential for organizations committed to maintaining high standards of safety and quality. The integration of advanced technologies, enhanced risk management frameworks, improved regulatory compliance, focus on cybersecurity, and enhanced training and development are some of the key updates that can significantly impact your operations. By embracing these updates, organizations can ensure and remain at the forefront of quality governance and operational safety management, thereby safeguarding their reputation and achieving sustainable success.
The Ministry of Public Health MOPH has recognized the transformative potential of digital health technologies and is making significant investments in this area. As healthcare systems around the world strive to become more efficient and patient-centric, digital health technologies offer promising solutions to many of the challenges faced by modern healthcare. This blog explores the reasons behind MOPH’s investments in digital health technologies and how these advancements are set to revolutionize healthcare delivery.
Enhancing Patient Care and Outcomes
One of the primary reasons MOPH is investing in digital health technologies is to enhance patient care and outcomes. Digital health tools, such as electronic health records (EHRs), telemedicine, and mobile health applications, enable healthcare providers to deliver more personalized and efficient care.
Electronic Health Records (EHRs): EHRs allow for better coordination among healthcare professionals, ensuring that patients receive comprehensive and consistent treatment.
Telemedicine: Telemedicine makes healthcare more accessible, particularly for individuals in remote or underserved areas, by allowing them to consult with specialists without the need for travel.
Mobile Health Applications: These apps provide patients with real-time access to their health data and enable continuous monitoring of health conditions.
Improving Healthcare Efficiency
Digital health technologies promise to improve the efficiency of healthcare systems. By automating routine tasks and streamlining administrative processes, these technologies can reduce the burden on healthcare providers and allow them to focus more on patient care.
Automated Scheduling Systems: These systems minimize the time spent on booking appointments.
Advanced Data Analytics: Data analytics help identify patterns and trends that inform better decision-making.
MOPH’s investment in these technologies is aimed at creating a more efficient healthcare system that can better manage resources and deliver higher quality care.
Promoting Preventive Healthcare
Digital health technologies are making a significant impact in preventive healthcare. Wearable devices and mobile health apps empower individuals to monitor their health in real-time and make informed decisions about their lifestyle and treatment options.
Wearable Devices: Track vital signs, physical activity, and other health metrics.
Mobile Health Apps: Provide valuable data that can be used to prevent diseases before they become severe.
MOPH’s focus on preventive healthcare through digital technologies is an important step towards reducing the overall burden of chronic diseases and promoting a healthier population.
Enhancing Data Management and Security
Effective data management and security are critical components of a modern healthcare system. Digital health technologies facilitate the secure storage and sharing of patient data, ensuring that healthcare providers have access to accurate and up-to-date information when making treatment decisions.
Secure Storage: Advanced data management systems improve the accuracy of medical records.
Data Security: Enhanced measures to protect patient privacy and data security.
MOPH’s investment in these technologies aims to build a more reliable and secure healthcare infrastructure.
Conclusion
MOPH’s investment in digital health technologies represents a significant commitment to transforming the healthcare landscape. By enhancing patient care, improving efficiency, promoting preventive healthcare, ensuring data security, supporting research, and addressing public health challenges, these technologies are set to revolutionize healthcare delivery. As MOPH continues to embrace digital health innovations, the future of healthcare looks promising, with the potential for improved outcomes and a more efficient and responsive healthcare system.
Aerospace engineering is a field where precision, safety, and reliability are paramount. Ensuring that materials, products, and processes meet stringent standards is critical for the success and safety of aerospace projects. The American Society for Testing and Materials ASTM plays a significant role in establishing these standards. In this blog, we will explore ASTM’s contributions to aerospace engineering and why they are essential for the industry.
What is ASTM?
ASTM International, formerly known as the American Society for Testing and Materials, is a globally recognized organization that develops and publishes voluntary consensus standards. These standards cover a wide range of materials, products, systems, and services, ensuring quality and safety across various industries, including aerospace engineering.
ASTM’s Impact on Aerospace Engineering
Material Standards
Selection and Specification: ASTM provides detailed standards for selecting and specifying materials used in aerospace applications. These standards ensure that these materials possess the necessary properties for high performance and safety.
Testing and Evaluation: Standards for testing and evaluating materials help in verifying their suitability for use in aerospace components. This includes tensile strength, fatigue resistance, and thermal stability.
Manufacturing Processes
Process Control: ASTM standards guide the manufacturing processes of aerospace components, ensuring consistent quality and performance. This includes standards for welding, machining, and additive manufacturing.
Quality Assurance: Standards for quality assurance processes help manufacturers maintain high levels of quality and reliability in their products, reducing the risk of defects and failures.
Component Testing
Performance Testing: ASTM provides standards for testing the performance of aerospace components under various conditions. This includes testing for structural integrity, thermal resistance, and vibration resistance.
Safety Testing: Standards for safety testing ensure that aerospace components meet strict safety criteria, protecting both the aircraft and its occupants.
Environmental Testing
Corrosion and Wear: ASTM standards address the testing of materials and components for corrosion and wear resistance, which are critical for the longevity and reliability of aerospace products.
Environmental Exposure: Standards for environmental exposure testing ensure that aerospace components can withstand extreme conditions such as high altitude, temperature variations, and humidity.
How METS Lab Supports Compliance with ASTM Standards?
At METS Lab, we understand the critical importance of ASTM standards in aerospace engineering. Our comprehensive testing and analytical services help the businesses to ensure their materials and components meet the stringent requirements set by ASTM. Here’s how we support compliance:
Advanced Testing Facilities: Our state-of-the-art laboratories are equipped to conduct a wide range of tests in accordance with ASTM standards.
Experienced Professionals: Our team of experts has extensive experience in aerospace testing and a deep understanding of ASTM standards.
Customized Solutions: We offer tailored testing solutions to meet the specific needs of our clients, ensuring accurate and reliable results.
Continuous Support: From initial consultation to final reporting, we provide continuous support to help our clients to navigate the complexities of ASTM compliance.
Conclusion
ASTM plays a vital role in aerospace engineering by providing comprehensive standards that ensure safety, reliability, and performance of materials and components. For international businesses involved in the aerospace industry, adherence to ASTM standards is crucial. METS Lab is committed to helping you to achieve compliance and excellence in aerospace engineering through our expert testing services.
The Saudi Standards, Metrology, and Quality Organization SASOsets the regulations and standards for products entering the Saudi Arabian market. Compliance with SASO requirements is essential for international businesses looking to operate in this region. In this blog, we will discuss how businesses can meet SASO standards and successfully navigate the compliance process.
Understanding SASO Requirements
SASO establishes guidelines to ensure the safety, quality, and efficiency of products. These requirements apply to a wide range of goods, including electrical appliances, automotive products, building materials, and more. Key components of SASO compliance include:
Product Standards: Ensuring that products meet specific safety and performance standards.
Conformity Assessment: Verifying that products conform the established standards through testing and certification.
Labeling and Documentation: Proper labeling and documentation to provide essential product information and evidence of compliance.
Steps to Meet SASO Requirements
Understand Relevant Standards
Identify Applicable Standards: Determine how SASO standards can be applicable to your products. This can be done by consulting SASO guidelines or working with a local expert.
Study the Requirements: Familiarize yourself with the specific requirements and specifications outlined by SASO for your product category.
Conduct Initial Assessments
Self-Assessment: Perform an internal review to assess whether your products meet SASO standards. Identify any gaps or areas needing improvement.
Consult Experts: Engage with regulatory experts or consultants who specialize in SASO compliance to get a comprehensive understanding of the requirements.
Product Testing and Certification
Choose an Accredited Lab: Select an accredited testing laboratory that is recognized by SASO to conduct the necessary tests.
Testing Process: Submit your products for testing to verify that they meet all requirements. Ensure that the testing covers all relevant aspects, such as safety, performance, and environmental impact.
Obtain Certification: Once your products pass the testing phase, obtain the necessary certification from the testing laboratory or relevant authority.
Prepare Documentation
Technical Documentation: Compile all technical documentation, including test reports, product specifications, and safety data sheets.
Compliance Certificates: Ensure you have the correct certificates of conformity, proving that your products meet SASO standards.
Labeling: Adhere to SASO’s labeling requirements, which may include specific markings, instructions, and safety warnings.
Register Products with SASO
Submit Documentation: Submit all required documentation and certifications to SASO for product registration.
Register Online: Use the SASO online portal (SABER) to register your products and manage compliance processes efficiently.
Stay Updated with Regulations
Regular Updates: SASO standards and regulations can change. Stay informed about updates and modifications to ensure ongoing compliance.
Continuous Monitoring: Implement a system for continuous monitoring of product standards and compliance requirements.
Benefits of Meeting SASO Requirements
Market Access: Complying with SASO standards is mandatory for entering and operating in the Saudi Arabian market, providing your business with access to a lucrative and expanding market.
Enhanced Product Quality and Safety: Adherence to SASO requirements ensures that your products meet high standards of quality and safety, reducing the risk of product recalls or safety issues.
Increased Consumer Trust: Compliance with recognized standards enhances consumer confidence in your products, leading to greater customer satisfaction and loyalty.
Regulatory Compliance: Avoiding fines, penalties, and legal issues by ensuring your products meet all regulatory requirements.
Conclusion
Meeting SASO requirements is a crucial step for international businesses aiming to operate successfully in Saudi Arabia. By understanding the relevant standards, conducting thorough assessments, obtaining necessary certifications, and staying updated with regulatory changes, businesses can ensure compliance and gain a competitive edge in the market. METS Lab is committed to assisting you in navigating the SASO compliance process with our expertise and comprehensive testing services.
REACH (Registration, Evaluation, Authorization, and Restriction of Chemicals) is a comprehensive regulation implemented by the European Union to ensure the safe use of chemicals within its territory. Compliance with REACH standards is essential for companies manufacturing, importing, or using chemicals in the EU. Effective training of your team on REACH compliance standards is crucial to meet these regulatory requirements. In this blog, we will guide you through the steps to effectively train your team on REACH compliance.
Understanding REACH Compliance
Before diving into the training process, it’s important to understand the basics of REACH compliance:
Registration: Companies must register chemicals they manufacture or import in quantities of one ton or more per year.
Evaluation: Submitted data is evaluated to assess potential risks.
Authorization: Certain hazardous substances require authorization for specific uses.
Restriction: Restrictions are imposed on the manufacture, placing on the market, or use of certain substances.
Steps to Train Your Team on REACH Compliance
Develop a Comprehensive Training Plan
Identify Key Roles and Responsibilities: Determine who needs training based on their roles. This includes regulatory affairs, quality control, production, and procurement teams.
Define Training Objectives: Establish clear objectives for what the training should achieve, such as understanding REACH requirements, knowing how to register substances, and recognizing restricted substances.
Engage Professional Trainers and Resources
Hire Experts: Engage REACH compliance experts or consultants who have extensive knowledge and experience in the field.
Utilize Online Resources: Take advantage of online courses, webinars, and e-learning platforms specializing in REACH compliance.
Create Tailored Training Modules
Introduction to REACH: Start with an overview of REACH regulations, including its purpose, scope, and key components.
Registration Process: Detailed training on the registration process, including data collection, dossier preparation, and submission.
Risk Management: Educate on identifying and managing chemical risks, including safety data sheets (SDS) and exposure scenarios.
Authorization and Restrictions: Explain the process for obtaining authorization for certain substances and understanding the list of restricted chemicals.
Hands-On Training and Workshops
Practical Exercises: Incorporate practical exercises and case studies to help employees apply what they have learned.
Interactive Workshops: Conduct workshops that allow for interactive learning, discussions, and Q&A sessions.
Regular Updates and Continuous Learning
Stay Current with Regulations: REACH regulations are subject to updates. Ensure your team is informed about any changes or new requirements.
Ongoing Training Programs: Establish continuous learning programs to keep your team updated on the latest REACH compliance practices.
Assess and Evaluate Training Effectiveness
Conduct Assessments: Regularly assess the knowledge and understanding of your team through quizzes, tests, and practical evaluations.
Gather Feedback: Collect feedback from participants to improve future training sessions.
Benefits of Effective REACH Compliance Training
Regulatory Adherence: Ensures your company complies with EU regulations, avoiding legal consequences.
Improved Safety and Risk Management: Enhances your team’s ability to manage chemical risks, ensuring a safer workplace and environment.
Enhanced Reputation: Demonstrates your company’s commitment to safety and regulatory compliance, enhancing your reputation among clients and partners.
Operational Efficiency: Streamlined processes and informed employees lead to more efficient operations and reduced risk of non-compliance.
Conclusion
Training your team on REACHcompliance standards is a critical step towards ensuring regulatory adherence and maintaining a safe and efficient workplace. By developing a comprehensive training plan, utilizing expert resources, and providing continuous learning opportunities, you can equip your team with the knowledge and skills needed to navigate REACH regulations effectively. METS Lab is here to support your compliance journey with our expertise and commitment to quality.
Microbiological testing plays a critical role in safeguarding public health. As a leading Microbiological Testing Lab, METS Lab is dedicated to providing top-notch analytical services to ensure the safety and quality of various products and environments. In this blog, we will explore the significance of microbiological testing and its impact on public health.
Understanding Microbiological Testing
Microbiological testing involves the detection, identification, and quantification of microorganisms in various samples. These microorganisms include bacteria, viruses, fungi, and parasites that can pose significant health risks if not properly managed. Testing is essential across numerous sectors, including food and beverages, pharmaceuticals, water treatment, healthcare etc.
Importance of Microbiological Testing in Public Health
Preventing Foodborne Illnesses
Contamination Detection:Microbiological testing lab like METS Lab play a crucial role in detecting contaminants in food products. This helps prevent foodborne illnesses caused by pathogens such as Salmonella, E. coli, Listeria etc.
Quality Control: Regular testing ensures that food manufacturers comply with safety standards, protecting consumers from potential outbreaks.
Ensuring Safe Drinking Water
Water Quality Testing: Contaminated water can lead to severe health issues, including gastrointestinal diseases and infections. Microbiological testing ensures that drinking water is free from harmful microorganisms.
Regulatory Compliance: Water treatment facilities rely on testing labs to meet stringent regulatory requirements, ensuring public safety.
Pharmaceutical Safety
Sterility Testing: In the pharmaceutical industry, microbiological testing is vital for ensuring the sterility of products, particularly injectable drugs. This prevents infections that could result from contaminated medications.
Product Stability: Testing helps in assessing the stability and shelf-life of pharmaceutical products by identifying potential microbial contamination over time.
METS Lab: Your Trusted Microbiological Testing Partner
At METS Lab, we pride ourselves on being a trusted partner in microbiological testing. Our state-of-the-art facilities and experienced professionals ensure that all testing is conducted with the highest level of accuracy and reliability. We offer a comprehensive range of services to meet the diverse needs of our clients, from routine testing to specialized analyses.
Advanced Technology: Our lab is equipped with cutting-edge technology to perform a wide array of microbiological tests, ensuring precise and timely results.
Expert Team: Our team of experts has extensive experience in microbiological testing, providing clients with valuable insights and recommendations.
Commitment to Quality: Quality is at the heart of everything we do. We adhere to stringent quality control measures to deliver results that our clients can trust.
Conclusion
Microbiological testing is essential for maintaining public health by ensuring the safety of food, water, pharmaceuticals, and healthcare environments. As a leading microbiological testing lab, METS Lab is dedicated to providing exceptional services that help protect communities from potential health risks. For reliable and accurate microbiological testing, trust METS Lab – your partner in public health safety.
FAIRS or exhibition, in the most general sense, is an organized presentation and display of a selection of items. Many FAIRS occurring in different regions for supporting and promoting the production of materials, introduction of new lab wares/equipments/chemicals/media/kits.
The Food Safety and Standards Authority of India (FSSAI) is a statutory body under the administration of the Ministry of Health and Family Welfare, Government of India. It regulates the manufacture, storage, distribution, sale, and import of food articles, while also establishing standards to ensure food safety. The FSSAI was established by the Food Safety and Standards Act, 2006, which consolidated all former acts and orders related to food safety that were previously handled by various ministries and departments. The FSSAI has its headquarters at New Delhi. The FSSAI provisions are enforced by Food Safety Officers.
The following are the statutory powers that the FSS Act, 2006 gives to the Food Safety and Standards Authority of India (FSSAI).
Framing of regulations to lay down food safety standards
Laying down guidelines for accreditation of laboratories for food testing
Providing about food safety and nutrition in India.
The ISI mark is a standards-compliance mark for industrial products in India since 1950. The mark certifies that a product conforms to an Indian standard (IS) developed by the Bureau of Indian Standards (BIS), the national standards body of India. The ISI is an initialism of Indian Standards Institution . The ISI mark is mandatory for certain products to be sold in India, such as electrical appliances including switches, electric motors, wiring cables, heaters, kitchen appliances, etc., and other products like Portland cement, LPG valves, LPG cylinders, automotive tyres ,etc. In the case of most other products, ISI marks are optional. ISI was founded to establish standards for the orderly growth of industries and for maintaining industrial output efficiency. It offers an ISI mark which is a standards-compliance mark for industrial products in India. ISI Marks means the products are checked for their quality.
Bureau of Indian Standards (BIS) is the National Standard Body of India. BIS is responsible for the harmonious development of the activities of standardization, marking and quality certification of goods and for matters connected therewith or incidental thereto.
BIS through its core activities of standardization and conformity assessment, has been benefiting the national economy by providing safe, reliable and quality goods; minimizing health hazards to consumers; protecting the environment, promoting exports and imports substitute; controlling over proliferation of varieties etc. The standards and certification scheme of BIS apart from benefiting the consumers and industry also support various public policies especially in areas of product safety, consumer protection, food safety, environment protection, building and construction, etc.
National Accreditation Board for Testing and Calibration Laboratories (NABL) is an accreditation body, with its accreditation system established in accordance with ISO/ IEC 17011. “Conformity Assessment –Requirements for Accreditation bodies accrediting conformity assessment bodies.” NABL provides voluntary accreditation services to:
Testing laboratories in accordance with ISO/ IEC 17025 ‘General Requirements for the Competence of Testing and Calibration Laboratories’
Calibration laboratories in accordance with ISO/ IEC 17025 ‘General Requirements for the Competence of Testing and Calibration Laboratories’
Medical testing laboratories in accordance with ISO 15189 ‘Medical laboratories -Requirements for quality and competence’
Proficiency Testing Providers (PTP) in accordance with ISO/IEC 17043 “Conformity assessment — General requirements for proficiency testing” and
Reference material producers (RMP) in accordance with ISO 17034 “General requirements for the competence of reference material producers”.
NABL is Mutual Recognition Arrangements (MRA) signatory to ILAC as well as APAC for the accreditation of Testing and Calibration Laboratories (ISO/IEC 17025), Medical Testing Laboratories (ISO 15189), Proficiency Testing Providers (PTP) (ISO/IEC 17043) and Reference materials producers (RMP) ( ISO 17034).
The disciplines and groups for which the accreditation services are offered in the respective fields are listed in –
NABL 120 “Guidance for Classification of Product Groups in Testing & Calibration field”
NABL 112 “Specific Criteria for Accreditation of Medical Laboratories”
NABL 180 “Application Form for Proficiency Testing Providers (PTP)”
NABL 190 “Application Form for Reference Material Producers Accreditation (RMP)”
Research and Development (R&D) represents the activities companies undertake to innovate and introduce new products and services or to improve their existing offerings. R&D allows a company to stay ahead of its competition by catering to new wants or needs in the market.
R&D activities differ from institution to institution, with two primary models[3] of an R&D department either staffed by engineers and tasked with directly developing new products, or staffed with industrial scientists and tasked with applied research in scientific or technological fields, which may facilitate future product development.
Research and development are very difficult to manage, since the defining feature of research is that the researchers do not know in advance exactly how to accomplish the desired result.
BTRA, a pioneer textile research institute over the 65+ years, was established in 1954 by Govt. of India along with the industry association to boost research, conducting testing, consultancy and certification in the field of textile, polymers, fibers and other materials. Currently it is partially funded by Ministry of Textiles, Govt. of India and its labs are approved and recognized by the Ministry of Textiles. We are the first MOT funded Center of Excellence (COE) for geotextiles in India and most sought-after Lab in India and neighboring country as far as technical textile is concerned.
The Synthetic & Art Silk Mills’ Research Association (SASMIRA) established on 12th January 1950 under Registration No. 2505 of 1949-1950 granted under societies act XXI of 1860 and is a cooperative venture set up by the man-made textile industry of India after independence as a multi-functional institute to serve its scientific and technological needs.
This proposal was supported by the Council of Scientific and Industrial Research (CSIR) and other Government agencies that culminated into establishment of SASMIRA, earlier known as Silk and Art Silk Mills’ Research Association.
SASMIRA’s Activities
Commencing with the testing of silk and art silk materials, SASMIRA has geared its activities since then to meet the changing needs of the man-made textile industry thereby fulfilling its objectives. At present, SASMIRA is an Approved Body of the Ministry of Textiles, Government of India. The major areas of functioning at SASMIRA are listed as below:
Northern India Textile Research Association (NITRA) is one of the prime textile research institutes in the country. The textile industry and Ministry of Textiles, Govt. of India jointly established NITRA in 1974 for conducting applied scientific research and providing support services to Indian textile industry. The organization is situated in a 50acre land at NCR Ghaziabad, near national capital New Delhi. It is certified by ISO 9001:2015. Today NITRA’s prime activities include research & development, technical consultancy, quality evaluation of materials, manpower training, third party inspection and publishing technical books and papers. NITRA also provides facilitating services to the decentralized powerloom sector through its eight centres located at Tanda, Kanpur, Meerut, Gorakhpur, Varanasi (all in U.P.), Panipat (Haryana), Ludhiana (Punjab) and Bhilwara (Rajasthan). NITRA is operating under the administrative control of Council of Administration comprising of representatives from Textile & Apparel industry, Govt. of India, trade associations, academic institutions and Textile Research Associations.
NITRA undertakes research projects in textile product development, machine design, instrument development and process development. NITRA also possesses patented technologies based on its R&D works. NITRA’s quality inspection & testing laboratories work 24×7 and analyze materials as per IS, ASTM, DIN, BS, ISO, JASO, AADTCC, EN and other customized standards.
For export to India, manufacturers need BIS certification (ISI) under Foreign Manufacturers Certification Scheme (FMCS), or BIS registration (CRS) for certain products. The BIS Certification is obligatory for these products, so that they can be introduced and sold on the Indian market. BIS Certification India or BIS Registration issued by the Bureau of Indian Standards (BIS) ensure the quality, safety and reliability of products in accordance with Indian Standards (IS). The Bureau of Indian Standards (BIS) is the national certification body in India under the umbrella of the Indian Ministry of Consumer Affairs, Food & Public Distribution. On April 1, 1987, it effectively replaced the Indian Standards Institution (ISI) organization and took over their functions.
There are three main types of certifications:
-BIS-Certification (ISI), Includes Factory Inspection (Scheme I, ISI Mark Scheme)
-BIS-Registration (CRS) Without Factory Inspection (Scheme II)
-BIS-Certification with Factory Inspection (Scheme X)
The BIS certification process always includes:
-Preparation of application documents and application at BIS
The U.S. Food and Drug Administration (FDA) is responsible for protecting public health by regulating imported products. Any company that plans to distribute food, animal, medical, or beauty products for the U.S. market is required to register with FDA.
If you produce products in the categories below, FDA registration may be mandatory:
Food, beverages, or dietary supplements
Cosmetic products
Animal and veterinary products
Medical devices
Drug products (including OTC)
Tobacco products
Radiation-emitting devices (RED)
Biologics
By registering your facility with FDA, you help to promote consumer safety and keep your company FDA compliant. FDA registration involves submitting detailed information about your products, manufacturing facilities and processes, quality control, labeling, recall procedures, and more.
The Federation of Indian Chambers of Commerce & Industry (FICCI) is a non-governmentaltrade association and advocacy group based in India. It is the largest, one of the oldest and the apex business organisation in India. It is a non-government, not-for-profit organisation. From influencing policy to encouraging debate, engaging with policy makers and civil society, FICCI articulates the views and concerns of industry. FICCI draws its membership from the corporate sector, both private and public, including SMEs and MNCs.
The Government of India has set up the Bureau of Energy Efficiency (BEE), also referred to as ‘BEE’ under the provisions of the EC Act, 2001 with the primary objective of reducing energy intensity of the Indian economy. The Standards and Labeling Scheme (S&L) is one of the major thrust areas of BEE. The mission of the Bureau of Energy Efficiency is to institutionalise energy efficiency services, enable delivery mechanisms in the country and provide leadership to energy efficiency in all sectors of the country. Its primary objective is to reduce energy intensity in the economy.
The broad objectives of BEE are as follows:
To exert leadership and provide policy recommendation and direction to national energy conservation and efficiency efforts and programs.
To coordinate energy efficiency and conservation policies and programs and take it to the stakeholders
To establish systems and procedures to measure, monitor and verify energy efficiency results in individual sectors as well as at a macro level.
To leverage multi-lateral, bi-lateral, and private sector support in implementation of Energy Conservation Act and efficient use of energy and its conservation programs.
To demonstrate delivery of energy efficiency services as mandated in the EC bill through private-public partnerships.
To interpret, plan and manage energy conservation programs as envisaged in the Energy Conservation Act.
To promote research and development in energy efficiency and energy conservation.
To develop testing and certification procedures for energy consumption of equipment and appliances and promote the testing facilities.
To strengthen consultancy services in the field of energy conservation.
Department of Healthcare Professions (DHP), Ministry of Public Health (MOPH) is the Sole authority responsible for the regulating of all healthcare practitioners working in both governmental and private healthcare sectors in the state of Qatar.
The Standards and Metrology Department, under the Qatar General Organization for Standards and Metrology (QS), prepares Qatar national standards and adopts international standards to be used as national standards for health, safety and the environment. The ASTM International MOU program is designed to encourage, increase and facilitate the participation of technical experts from around the world in the ASTM standards development process.
This year, QS referenced 233 ASTM International standards in Qatar regulations. The referenced standards cover plastics, plastic piping systems and concrete and concrete aggregates. Several technical experts from Qatar participate on one or more of ASTM’s 142 standards development committees, and QS has participated in various ASTM technical training programs through the MOU program.
