Yes

China Food and Drug Administration’s (CFDA’s) – GMP for Medical Devices

21 CFR Part 211 Subpart D – Equipment

Data Integrity Awareness: Good Documentation Practices

Data Integrity Awareness: ALCOA+

EU Medical Device Regulation (EU MDR) – Chapters 1 to 5

Data Integrity Awareness: Health Authorities

Data Integrity Awareness: An Introduction

Ensuring Environmental Quality: A Guide to Microbiological Monitoring

EU Medical Device Regulation (EU MDR) – Chapter I: Scope and Definitions

EU Medical Device Regulation (EU MDR) – Introduction