Packaging Design Validation Testing
Manufacturers of medical devices need to ensure their terminally sterilized products are contained in validated packaging. Attendees of this webinar will learn about packaging design considerations and various package testing including shelf-life, distribution, strength, integrity, and microbial barrier.
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Validating, Optimizing and Monitoring EO Sterilization Processes, Day 1
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Package Validations – Meeting the Requirements of ISO 11607
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Medical Devices Regulation Training
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Review of Medical Packaging Materials & Converting Processes
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Pharmaceutical Manufacturing: Solving Common Fill-Finish Challenges
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Design Controls - Requirements for Medical Device Developers
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Understanding Ethylene Oxide Sterilization
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Ethylene Oxide Sterilization Validation
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Medical Device Packaging as Told Through Design Control
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How to Categorize a Medical Device per ISO 10993-1
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Process Validation for Medical Device Manufacturers
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Process Validation Procedure for Medical Device Manufacturers
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Understanding Europe's Medical Device Regulation
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PLC Troubleshooting 101. Basic Steps to Diagnose and Fix Your Machine
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What do tech pioneers think about the AI revolution? - The Engineers, BBC World Service
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Developing Biocompatibility for Medical Devices - Audrey Turley
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Design Control for Medical Devices - Online introductory course
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Discover Aseptic Fill-Finish – A Critical Step in Parenteral Manufacturing
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Webinar - Understanding vibration and mechanical shock
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