Intertek India’s Post

Quality Professionals who have jumped industries: Do you feel like your experience in one or more ISO standards, general quality principles, and understanding of regulatory requirements is transferable between different industries (including ones utilizing additional lSO standards or CFR titles)?

Quality is our promise, and precision is our standard. Explore our quality control and assurance services, where every component undergoes rigorous testing, inspection, and certification to ensure unmatched quality and reliability. Trust us to deliver precision perfection every time. 📞 01274 048555
 📩support@global-precision.co.uk 🌐 link in the comments #QualityControl #GlobalPrecision

While operating in several areas, EQS is always concerned with continuously improving quality standards and performance for its clients. We know that inspection is a fundamental step, which is why our experts are always ready to help you reduce risks and improve processes and quality throughout the chain. Find out more about quality control ➡️ https://bit.ly/3y9Pu39 #EQS #EQSGlobal #ExpertiseWithMeaningfulImpact #EQSMozambique #qualitycontrol #certification #procedures #inspection 

ISO 17025 is an international standard that outlines the general requirements for the competence of testing and calibration laboratories. Here are 50+ terms associated with ISO 17025 along with brief definitions:

To systematically evaluate the effectiveness and implementation of the quality objectives and stringent requirements outlined by ISO 9001 standard, an internal audit was conducted at Omera Cylinders premises. #Internal_audit #ISO_9001 #Omera_Cylinders #Omera_LPG

Experience the Advantages of IECQ QC 080000 Certification with DQS India! In today’s rapidly evolving world, ensuring the quality and safety of your electronic products is crucial. That’s where IECQ QC 080000 certification comes in. IECQ QC 080000 is a globally recognized standard that focuses on the management of hazardous substances in the electronics industry. It helps companies meet regulatory requirements, reduce risks, and improve product quality by ensuring compliance with environmental, health, and safety standards. Why should your business consider IECQ QC 080000? ✅ Ensure Compliance with global standards for hazardous substance management in electronic products. ✅ Enhance Product Safety by reducing the risk of non-compliance and unsafe materials in your products. ✅ Boost Reputation with stakeholders, customers, and regulators by showcasing your commitment to quality and environmental responsibility. ✅ Access New Markets as more businesses are prioritizing sustainability and regulatory adherence. At DQS India, we specialize in helping organizations achieve IECQ QC 080000 certification with our team of highly qualified auditors. With our comprehensive support throughout the certification process, we ensure a smooth journey towards compliance, so your company can confidently meet industry requirements. Interested in learning more? DM us today to explore how DQS India can assist you in obtaining IECQ QC 080000 certification and help your business stand out in the global market. #IECQ #QC080000 #ElectronicsIndustry #HazardousSubstanceManagement #DQSIndia #Certification #ProductSafety #QualityManagement #EnvironmentalCompliance #Sustainability

Available in Europe too!

When applied in a GLP context risk is defined as the combination of the probability of issues or problems occurring (within a test facility, quality system or study), the impact these may have on the integrity of the data and the overall GLP compliance of the facility, quality systems or study. Dear SQA colleagues,  for insight of Risk assessment take an opportunity to look at the poster presentations (P-13, P-26, P-31, and P-33) and podium presentation in Session P during 40th Annual meeting of Society of Quality Assurance (SQA-2024), April 7-11, 2024 at Aurora, Colorado, USA. #SQA2024, #JRFGlobal

QPS Team delivers! you can get a quote in less that 72 Hours and the FC process within 1 to 2 weeks

Required information for external providers and how the organization could monitor, evaluate and review their performance. 1- Required information -The processes, services, and products to be provided. -The approval of products, services, the methods, processes and equipment, and the release of products and services. -Competence including any required qualification of persons. -The external providers interactions with the organization. -Control and monitoring of the external provider’s performance to be applied by the organization. -Verification or validation activities that the organization or its customer intends to perform at the external providers premises.  2-Monitoring and Performance Evaluation through: Incoming Inspections: Sample Inspection: Conducting random or statistical sampling of received components to assess overall quality. Certificate of Conformance or conformity (CoC) Review "second party audit": Verifying the supplier's CoCs to ensure they meet the agreed-upon specifications. Testing: Performing specific tests on the components to confirm their functionality and performance. 3- Supplier Performance Reviews such as: Regularly assess the supplier's performance based on metrics aligned with the communicated requirements, potentially including; On-Time Delivery Rates: Track the supplier's ability to deliver components according to agreed-upon schedules. Quality Defect Rates: Monitor the number of non-conforming components received from the supplier. Responsiveness to Issues: Evaluate how promptly the supplier addresses any quality concerns or production problems. #externalproviders #qualitymanagementsystem #ISO9001