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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
Presenter: Andrew Thomas
Presenter: Andrew Thomas
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)

REGISTER TODAY to Reserve Your Spot

Past Webinars

Gross Leak Detection vs. Dye Penetration for Medical Device Package Testing

Top Failures During Gross Leak Detection and Seal Strength Testing of Medical Device Packaging

Medical Device Package Distribution Testing per ASTM and ISTA

Amazon Package Certification Update - December 2018

Sterile Barrier Testing Case Studies

ISTA 6-Amazon Packaging Solutions

Case Studies of Medical Device Package Failures

Sample Size Rationale for Medical Device Package Validation

The Shocking Truth About the Frequency Domain

ASTM vs ISTA for Package Testing - Which Is Better?

Accelerated and Real Time Aging

Top Five Package Design Mistakes

Riveting Revisions of Medical Product Package Test Procedures

Product and Package Shock Testing

Product and Package Vibration Testing

Hazardous Material Package Certification Overview

Packaging Dynamics #6 of 5: Extra Credit - Tricks of the Trade

Packaging Dynamics #5 - Design and Testing of the Protective Package System; How We Know When the Job Was Done Correctly

Medical Device Packaging Testing - Common Test Failure Modes & Solutions

Packaging Dynamics Webinar #4 - Dynamic Cushion Testing for Shocking Absorption & Vibration Attenuation

Product Reliability Testing - Mechanical and Environmental Testing for a Rackmount Network Switch

Packaging Dynamics Webinar #3 - Determining the Vibration Sensitivity & Shock Fragility of Products; Test Methods, End Results, and Significant Insight

Packaging Dynamics Webinar #2 - Defining & Quantifying the Distribution Environment Through Which All Products Must Travel

Riveting Revisions of Medical Package Test Procedures

Packaging Dynamics Webinar #1 - Overview and Definition of Terms

Arrhenius Equation Demystified - Usage with Accelerated Aging of Medical Device Packaging

Writing Test Validation Protocol Per ISO 11607 to Minimize Time to Market

Package Integrity Testing: Common Tests and Applications

Product Mechanical Shock and Fragility Testing Overview

Supply Chain: Dimensional Weight Pricing - What Does This Mean and How Can We Avoid Large Logistics Cost?

Medical Device Package Validation: Review and Updates on Standardized Test

Product Reliability: Combined Environmental Conditions Testing

Product Reliability Testing: Environmental and Mechanical Requirements

Packaging Integrity Testing, Optimizing Packaging and Minimizing Waste

Developing and Evaluating the Optimal Package

Sterile Barrier System Testing Failure Modes and Design Recommendations

Applying Damage Boundary Principles to Save Product and Package Costs