Life Science Outsourcing

ASTM F88 Explained: Peel Strength Testing for Medical Device Packaging

Peel strength testing is critical to ensuring the integrity and safety of sterile medical device packaging — and ASTM F88 is the industry standard that guides how it’s done.

FDA-Registered Manufacturing FacilityISO 13485 Certified Quality System12 Cleanrooms Class 5–8125,000+ Sq Ft Regulated Manufacturing3 Facilities CA | NH | Costa Rica

Peel strength testing is critical to ensuring the integrity and safety of sterile medical device packaging — and ASTM F88 is the industry standard that guides how it’s done. In this short explainer video, Life Science Outsourcing (LSO) walks you through:

  • What ASTM F88 is and why it matters for sterile barrier packaging
  • How peel strength testing works and what it measures
  • Why compliance is essential for meeting FDA and ISO 11607 requirements
  • How LSO helps you validate packaging performance efficiently and accurately

With over 25 years of experience in medical device assembly, packaging, sterilization, and validation testing, LSO offers a one-stop solution to accelerate your go-to-market timelines while maintaining the highest quality and regulatory standards. If you’re preparing your device for FDA submission or ISO compliance, understanding ASTM F88 is key — and LSO is here to help. Learn more about our packaging validation services: https://www.lso-inc.com/packaging-validation

FDA-Registered

Manufacturing Facility

ISO 13485

Certified Quality System

12 Cleanrooms

Class 5–8

125,000+ Sq Ft

Regulated Manufacturing

3 Facilities

CA | NH | Costa Rica