Life Science Outsourcing

Packaging Standards for Medical Device Safety

Learn about packaging standards and their importance in ensuring the safety and performance of medical devices over time.

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

Medical Package Testing Standards

Both the FDA and international regulatory bodies emphasize on compliance with ISO 11607; Packaging for Terminally Sterilized Medical Devices. This standard defines the test requirements necessary to ensure that the terminally sterilized package/device will maintain its design performance over the intended life of the product and will not degrade as a result of sterilization, shelf life, transport, or storage.

  • ANSI
    American National Standards Institute
  • AAMI
    Association for the Advancement of Medical Instrumentation
  • ASTM
    American Society for Testing & Materials
  • ISO
    International Organization for Standardization
  • ISTA
    International Safe Transit Association




Standards Expertise

Package Testing Standards Organizations

Life Science Outsourcing is experienced in package testing that must comply with the following standards:

ASTM Standards

 

ISTA Standards

ISO Standards

On this Page

All Standards

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