Make sure your medical devices meet customer, quality and regulatory standards with our Process Validation for Medical Devices Training Course. This course is a must for all involved in manufacturing, regulation and development - and will help you quickly meet ISO 13485, EU and Food and Drug Administration (FDA) requirements.
Validating medical devices need not be complex when you understand all that's involved. Working with us you can get to grips with regulatory and safety standards and quality assurance. You will become confident developing devices in line with the FDA's Quality System Regulation and ISO 13485 - reducing development time and gaining earlier access to market.