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Access Meditrial Academy to learn quickly and easily the details of the new Medical Device Regulation (MDR) 745/2017. Everything you need to know about the MDR and how to apply it to a device and company.
Revisions to the ISO 14155 standard covering pre- and post-market clinical investigations for medical devices are expected in 2019. The updated standard contains key changes that impact the clinical trial design and conduct, risk management, data capture and safety assessments.
Explore these changes to get ready!