Yes

EU Medical Device Regulation (EU MDR) – Chapter 5: Classification and Conformity

21 CFR Part 50 Subpart B: Informed Consent of Human Subjects [Part 1]

The Basics of Laboratory Investigations

ISO 14971:2019: The Evolution and Definitions

Computer System Validation – Risk Management

MDSAP Country Specific Requirements (Canada)

EU Medical Device Regulation (EU MDR) – Chapter 4: Notified Bodies

ISO 14971 – The Scope of the Standard

MDSAP Country Specific Requirements (USA)

An Introduction to Medical Device Validation – Part 3