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 MemberSource: 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, 2024What's the difference between PDCA and a Management System?July 25, 2024Classification of Medical Devices under EU MDRAugust 21, 2024100 quality tools in 200 minutes: How Fishbone Diagram Tackles Root CausesSeptember 25, 2024Why Formal Quality Management Does Not Work in Public SectorOctober 9, 202414 Pointless Tasks Quality Managers Wish They Could SkipOctober 9, 2024Five Steps to Prove Consideration in Quality ManagementOctober 9, 2024ISO 9001 Revision Pushed to 2026?September 4, 2024"Made in Germany" losing ground as companies look abroadAugust 20, 2024Adopting GHG Standards Boosts Business SuccessOctober 16, 2024