Post Market Surveillance under EU MDR 2017/745 Training
Post Market Surveillance (PMS) under the EU Medical Device Regulation (MDR) Training is designed to equip quality and regulatory professionals, medical device manufacturers, and post-market teams with the knowledge and tools to meet these rigorous requirements.
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2025 Training Guide
Innovation Leaders for ISO Standards, Auditing & Medtech QA/RA Training
Michelle Keane discusses CAPA in Medical Devices including potential reasons organizations struggle and the FDA raise so many findings in this area....
As per ISO 13485, is it true or false that a medical device organization that uses spreadsheets is only required to validate spreadsheets that contain...
Comply Guru proudly sponsored Global Access 2024 which is 's largest conference for Quality and Regulatory Affairs Professionals in Medical Devices....
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