Pharmaceutical packaging
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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.
Examples
-
Tablets in a blister pack in folding carton
See also
- Authentication
- Child-resistant packaging
- Cold chain
- Contamination control
- Counterfeit medications
- Good Distribution Practice
- Good manufacturing practice
- International Pharmaceutical Federation
- Package pilferage
- Package testing
- Pharmacopoeia
- Shelf life
- Tamper-evident
- Tamper resistance
- Track and trace
- Verification and validation
- Validation (drug manufacture)
General references
- anon, Guidance for Industry:Q8 (R2) Pharmaceutical Development, US FDA, 2009, [1]
- 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