Yes

21 CFR Part 211 Subpart D – Equipment

Data Integrity Awareness: Good Documentation Practices

Restricted Access Barrier Systems (RABS) Glove Training

Data Integrity Awareness: ALCOA+

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

Data Integrity Awareness: Health Authorities

An Introduction to Data Integrity Awareness

Microbiological Environmental Monitoring

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

EU Medical Device Regulation (EU MDR) – Introduction