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Packaging Shelf Life

Packaging Shelf Life

The Packaging Shelf Life test is a real-time evaluation of a material’s sterile barrier. It is used to demonstrate that wraps will maintain a sterile barrier over time and complies with the Association of Operating Room Nurses (AORN) standard. Nelson Laboratories has more than 25 years of experience performing this test, and we can help clients prepare for the test and act on the results.  Sterilization validations and penetration studies should be completed prior to shelf life testing to establish the sterilization cycle parameters.

Applicable Standards

  • ISO 11607

Test Options

Ask an expert for a specific consultation on your product. If you are ready to submit your samples for testing, click here to fill out the Sample Submission Form.

Code Test Request Quote
ERS160 Packaging: Event Related Sterility Assurance, Custom Interval, No Predicate Add
ERS260 Packaging: Event Related Sterility Assurance, Custom Interval, w/ Predicate Add
ERS160 - Packaging: Event Related Sterility Assurance, Custom Interval, No Predicate
ERS260 - Packaging: Event Related Sterility Assurance, Custom Interval, w/ Predicate

Sample Specifications

ERS160: Each sheet should be 18” x 18” minimum Double wrap, single use – 70 material Single wrap, single use – 35 material
ERS260: Each sheet should be 18 x 18 minimum Double wrap, single use 70 material + 70 predicate Single wrap, single use – 35 material + 35 predicate

Study Outline

The Packaging Shelf Life study is designed to simulate the use of the products in a hospital or clinical situation.   Test packs are prepared by the lab according to sponsor specifications and placed on the shelf for the designated storage interval.  Typical storage intervals are 30, 60, 90, 180 and 365 days.  A typical pack consists of a sterile barrier system (wrap, tray, pouch, etc.) that contains a product (actual product, mock product, coupons, or gauze).  Biological and chemical indicators (BIs and CIs) are typically included to verify that the packs were adequately sterilized.  
AORN’s recommended sterilization practices define event-related sterility as “Shelf life based on the quality of the packaging material, storage conditions during transportation and amount of handling of item.” They suggest that the following factors affect shelf life:
  • Type and configuration of packaging materials
  • Number of times a package is handled before use
  • Number of personnel who may have handled the package
  • Storage on open or closed shelves
  • Condition of storage area (cleanliness, temperature, RH)
  • Use of dust covers and method of sealing
Our shelf life procedures integrate weekly handling and rotation in addition to the normal post-sterilization handling transfer to the storage shelves. All shelf life packs are stored on open wire shelves, which permit the highest levels of microbial fallout. The cleanliness of the environment is monitored weekly using both passive (fallout) and active (Anderson sampler) collection techniques.  Temperature and relative humidity (RH) are recorded weekly to provide full environmental storage records.

After the designated storage interval, the packs are transferred to our sterility suite where the contents are tested using traditional USP sterility parameters.  Packs with actual product are tested in the same manner as routine lot release samples.  Samples with mock product or coupons are generally subdivided into quadrants with some quadrants tested in SCDB and some in THIO.

Recommended replicates: The number of packs to test at each storage interval is left to the discretion of the sponsor.  Historically, sets of 3 to 30 have been tested.  We recommend preapproving the test plan, including the number of samples with the FDA prior to test initiation.

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