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Decisive Brunt of Physical and Chemical Exploration on Pharmaceutical Sterile Containers
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 Clean room. The Code of federal regulation, Title 21, Drug current good manufacturing pract...
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Published in: | Asian Journal of Pharmaceutical Analysis 2018-09, Vol.8 (3), p.140 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | 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 Clean room. The Code of federal regulation, Title 21, Drug current good manufacturing practice in manufacture, Processing, Packaging or Holding requires that containers, closure and component parts that they are not reactive, additive or absorptive to an extend that significantly affect the identity, strength, quality or purity of the drug and furnish adequate protection against its deterioration or contamination. Basic polymer, residual monomer, plasticizers, accelerators, modifiers, stabilizers, fillers, colourants, antistatic agent, slip or anti-slip additives, U.V absorbers, lubricants, antioxidants [12]. Pharmaceutical packaging technology is structured to meet the needs of the global market, and assesses a wide range of current knowledge, catering for the requirements of the pharmaceutical industry as well as for pharmaceutical companies in emerging nations who are still seeking a basic grounding in the subject. |
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ISSN: | 2231-5667 2231-5675 |
DOI: | 10.5958/2231-5675.2018.00026.1 |