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
Comply Guru proudly sponsored Global Access 2024 which is Ireland's largest conference for Quality and Regulatory Affairs Professionals in Medical Dev...
On 30th October 2023, IRCA formally certified Comply Guru's latest Blended Learning offering, a Combined ISO 14001 and ISO 45001 Lead Auditor Training...
Let's talk about Blended Learning. In 2019, Comply Guru set out to create a new approach to conventional Auditor Training, launching it's first CQI & ...
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