Yes

ISO 13485:2016 – Measurement Analysis and Improvement (Chapter 8 – Part A)

ISO 13485:2016 – Product Realization (Chapter 7 – Part B)

Pharmaceutical Microbiology and Industry Considerations

Medical Device Single Audit Program (MDSAP) – Part 1

Good Manufacturing Practices – Good Practices and Quality Control

The Basic Principles of Isolator Technology

ISO 13485:2016 – Chapter 4: The Quality Management System (QMS)

ISO 13485:2016 Product Realization (Chapter 7 – Part A)

Computer System Validation – Requirements: The Basis for Validation

ISO 13485:2016 – Chapter 6: Resource Management