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.
CourseBy Amalia Tammam
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.
CourseBy Rami Azulay
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