Management Systems World
All on Quality and other Standards in one place since 2010. Now Worldwide.
Licensing or Accreditation: The Crucial Choice for New Ventures in Pharma and Medical Devices
September 4, 2024
You are not permitted to access this page. Please purchase membership to get full access to all articles.
Become a Member
Source: Quality Systems Now’
When launching Greenfield projects in the pharmaceutical or medical device industries, businesses often face the decision between Good Manufacturing Practice (GMP) licensing and ISO 13485 accreditation.
Most popular blogs
-
Understanding NDC in Measurement System Analysis - Automotive Quality SolutionsJuly 2, 2024ISO 9001 Revision Pushed to 2026?September 4, 2024Classification of Medical Devices under EU MDRAugust 21, 2024100 quality tools in 200 minutes: How Fishbone Diagram Tackles Root CausesSeptember 25, 2024What's the difference between PDCA and a Management System?July 25, 2024Avoiding Common Pitfalls in ISO 27001 ImplementationJanuary 21, 2025Writing Clear Control Descriptions for SOC 2 and ISO 27001 with Expert PrecisionMarch 11, 2025Auditing: Finding Faults or Issuing Opinions?October 30, 2024Introducing the ISMS Copilot X, a cross-framework assistantJuly 25, 2024ISO 9001 Revision Criticized for Diluting Quality StandardsDecember 10, 2024
