Yes

Medical Device Single Audit Program (MDSAP) – Part 3

21 CFR Part 820 Subpart 0 – Statistical Techniques

21 CFR Part 820 Subpart N – Servicing

21 CFR Part 820 Subpart M – Records

21 CFR Part 820 Subpart L – Handling, Storage, Distribution and Installation

21 CFR Part 820 Subpart K: Labeling and Packaging Control

21 CFR Part 820 Subpart J – Corrective and Preventive Action

Medical Device Single Audit Program (MDSAP) – Part 2

The Devastating Effects of Not Following GMP

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