If you want to outsource your medical devices test activities you must make sure that the data and reports you receive are accurate and meet the Medical Devices regulatory requirements for testing EN 17025 and Good Laboratory Practice (GLP) as well as ISO 13485. A Testing Agr Show all details
From both a regulatory and commercial perspective, companies should work with their suppliers (contract manufacturers) to ensure that they receive materials and services in line with predetermined specifications covering quality, volume and delivery. Some companies limit the Show all details
This ready-to-use quality audit questionnaire (audit by mail) has been created to assess potential contract manufacturers and judge their ability to meet current GMP. This questionnaire also includes a covering letter, which needs only a small amount of modification before it Show all details
This ready-to-use quality audit questionnaire (audit by mail) has been created to assess potential contract laboratories, to test their quality standards and regulatory profile and reassure your company that the contract laboratory is able to operate in line with current good Show all details
On this page you can purchase Quality Contracts and Agreements.