Hostname: page-component-8448b6f56d-c47g7 Total loading time: 0 Render date: 2024-04-19T04:32:27.659Z Has data issue: false hasContentIssue false

Stability Testing, Shelf Life and Product Expiration Dating

Published online by Cambridge University Press:  14 March 2018

Peter A. Takes*
Affiliation:
Sterotaxis, Inc.

Extract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Reagents available for laboratory, research, and clinical use are often acquired with a specified expiration date. Yet, many are not, depending on the manufacturer and reagent type. What a manufacturer does is frequency determined by how they label the product.

The U.S. Ricd and Drug Administration [FDA] has defined categories by which reagents can he labeled based on their “intended use”. individual reagents (e.g., antibodies) intended for clinical diagnostic laboratory use will be labeled as an in Vitro Diagnostic [IVD] or Analyte Specific Reagent [ASR]. Under these categories, specified expiration dates must be supported by stability testing which establishes the product shelf life.

Type
Research Article
Copyright
Copyright © Microscopy Society of America 1998

References

1. Takes, P.A., and Murray, G.. 1998. The analyte specific reagent rule - a new set of regulations for labs, manufacturers. Clin Lab News 24(4): 10.Google Scholar
2. Takes, P.A. 1998. What's in a label? Clin Lab News 24(4):10.Google Scholar
3. Jackson, C.M. 1997. Meeting the challenge of stability. JVD Technol 3(3): 3848 Google Scholar
4. Clark, G.S. FDA Guidance Document: Sheir Life of Medical Devices, DSMA, CDRH, FDA, April. 1991.Google Scholar
5. Title 21 Code of Federal Regulations, Section 809.10Google Scholar
6. Donohue, J., and Apostolou, S.. 1998. Predicting the siielf life from accelerated aging data: Ihe D&A and variable Q10 techniques. Med Dev Diag Ind 20(6): 6872 Google Scholar
7. USP 23/NF 18, pp. 1962-1963 (1995).CrossRefGoogle Scholar
8. Franks, F. 1994. Accelerated stability testing of bioproducts: attractions and pitfalls, Trends Biotechnol 12. 114117.CrossRefGoogle ScholarPubMed
9. Golden, M.H., et al. 1996. A matrixed approach to long-term stabilily testing of pharmaceutical products. J Pharm Sci 85(2) 240245.CrossRefGoogle Scholar
10. Title 21 Code of Federal Regulations Part 820.Google Scholar
11. Hemmerich, K.J. 1998. Genersl aging theory and simplified protocol for accelerated aging of medical devices. Med Plast Biomat 5(4): 1623.Google Scholar