Pharmaceutical packaging
From Wikipedia, the free encyclopedia
Pharmaceutical packaging has to be carried out for the purpose of the safety of the pharmaceutical preparations in order to keep them free from contamination, hinder microbial growth, and ensure product safety through the intended shelf life for the pharmaceuticals. Packaging is a critical tool in the pharmaceutical industry for product delivery and regulatory compliance, many pharmaceutical companies will do all their packaging within a contamination free environment or Cleanroom. Some common pharmaceutical packaging techniques include foil and heat sealing; polyester and olefin package printing; polyethylene and polypropylene printing; and flat bed die cutting.
See also
- Authentication
- Child-resistant packaging
- Cold chain
- Counterfeit medications
- Good Distribution Practice
- International Pharmaceutical Federation
- Package pilferage
- Package testing
- Pharmacopoeia
- Shelf life
- Tamper-evident
- Tamper resistance
- Track and trace
- Verification and validation
General references
- anon, Guidance for Industry:Q8 (R2) Pharmaceutical Development, US FDA, 2009,
- Dean, D. A., 'Pharmaceutical Packaging Technology", 2000, ISBN 0-7484-0440-6
- Lockhart, H., and Paine, F.A., "Packaging of Pharmaceuticals and Healthcare Products", 2006, Blackie, ISBN 0-7514-0167-6
- Pilchik, R., "Validating Medical Packaging" 2002, ISBN 1-56676-807-1
- Rosette, J. L, "Improving Tamper-Evident Packaging: Problems, Tests and Solutions", 1992
- Soroka, W, "Fundamentals of Packaging Technology", IoPP, 2002, ISBN 1-930268-25-4
- Yam, K. L., "Encyclopedia of Packaging Technology", John Wiley & Sons, 2009, ISBN 978-0-470-08704-6
This article is issued from Wikipedia. The text is available under the Creative Commons Attribution/Share Alike; additional terms may apply for the media files.