Balancing Data with Risk to Improve Patient Safety
WESTPAK joins industry peers from DuPontTM and Eagle Medical, Inc. in presenting “Balancing Data with Risk to Improve Patient Safety.”
Attendees will learn about:
“Validated Testing for Medical Device Packaging” from Andrew Thomas, Lab Manager, WESTPAK
“Battle for Perfect Information” from Roy Morgan, PE, PMP, Vice President of Engineering & NPI, Eagle Medical, Inc.
“Sterilization Industry Challenges” from Dan Floyd, MDM & Regulatory Specialist, DuPontTM Tyvek® Medical & Pharmaceutical Packaging
Andrew Thomas’ “Validated Testing for Medical Device Packaging” Covers:
- Regulatory Requirements for Validated Testing
- Validation of Test Methods
- Validated Package Tests
Lab Manager, WESTPAK
Andrew’s Presentation Will Provide Participants With:
- Brief review and rationale of the regulatory requirements for validated testing
- Overview of test method validation practices at WESTPAK
- List of package tests recommended for validation
Who Should Benefit From Attending:
- Project and Program Managers
- Quality / Reliability Staff
- Packaging Engineers
- Buyers
Date: Wednesday, January 27, 2021
Time: 10 – 11:30 am PST / 1 – 2:30 pm EST
Price: No Charge
Note: Register for this webinar at DuPontTM’s page (link below)