45 mins

ISO 13485:2016 – Chapter 6: Resource Management

ISO 13485:2016 – Chapter 5: Management Responsibility

ISO 13485:2016 – Chapter 1-3: Introduction

Computer System Validation (CSV) – Basic Concepts, Regulations and GAMP®5

Microbiological Contamination of Pharmaceutical Products – Part 1

21 CFR Part 820 Subpart H – Acceptance Activities

21 CFR Part 820 Subpart G – Production and Process Controls

How To Be An Effective GMP Auditor – Part 3

How to be an Effective GMP Auditor – Part 1

21 CFR Part 820 Subpart E – Purchasing Controls