What Medical Device Manufacturers Can Learn from 21 CFR Part 211 Subpart D - Manufacturing Equipment Management
This course focuses on providing an understanding of the U.S. Food and Drug Administration’s current Good Manufacturing Practices (cGMP) regulations for equipment used for medical devices/drug manufacturing and related processes.
- Course
- By Rami Azulay
eQMS - eForm - ISO 13485/21 CFR Part 820 Subpart J - Corrective and Preventive Action CAPA Management (User)
Edition II (Nov. 2023) Learn how to manage CAPA using Orcanos eForms module.
- Course
- By Amalia Tammam