EAG Successfully Completes ISO 17025 Accreditation Expanding Scope to RGA Testing

and it is a requirement for many regulatory agencies. This accreditation provides the assurance that the testing laboratory has the necessary competence to perform testing and calibration services accurately and consistently. Second, it demonstrates that the laboratory has a robust quality management system in place. RGA testing at EAG  recently achieved the required suitability to perform MIL-STD testing. Now, with RGA included in the scope of ISO 17025, RGA testing at EAG is a premium choice to perform gas analysis. Medical device manufacturers are increasingly opting for ISO 17025 vendors/suppliers because they need to ensure that the components and materials used in their products meet the required quality standards. By working with an accredited vendor/supplier, medical device manufacturers can reduce the risk of product recalls and other issues that may arise. Some additional benefits of ISO 17025 accreditation include medical device manufacturers include increased confidence in the quality of test and calibration results, increased market opportunities, improved customer satisfaction, and reduced costs.

For medical devices and biomaterial companies, EAG offers the most diverse and comprehensive suite of testing and engineering support available. EAG Laboratories has established itself within the technology and biomedical space by developing scientific expertise in difficult analytical measurements, characterizations of complex materials and systems, and a pioneering approach to problem-solving. Contact us today to learn more about how EAG’s ISO 17025 Accreditation would be a benefit for you.