45 mins

21 CFR Part 211 Subpart B: Organization and Personnel

21 CFR Part 211 Subpart K – Returned and Salvaged Drug Products

Data Integrity Awareness: CSV Best Practices

21 CFR Part 211 Subpart D – Equipment

Data Integrity Awareness: Health Authorities

An Introduction to Data Integrity Awareness

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

21 CFR Part 211 Subpart E – Control of Components, Drug Product Containers and Closures

21 CFR Part 211 Subpart G: Packaging and Labeling Control

21 CFR Part 211 Subpart C – Building and Facilities