Ron Scarboro, Azurity Pharmaceuticals, explains when formulation robustness justifies added cost and which post-approval quality and supply metrics teams can track.
News|Articles|November 2, 2004
- Pharmaceutical Technology-11-02-2004
- Volume 28
- Issue 11
Comparing and Contrasting Barrier Isolator Decontamination Systems
A discussion of the validation and operation of two commercially available vapor-phase hydrogen peroxide decontamination systems is presented, based on a hands-on examination of both systems.
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Articles in this issue
almost 22 years ago
Still Waiting for Answersalmost 22 years ago
Method Validation by Phase of Development: An Acceptable Analytical Practicealmost 22 years ago
November 2004almost 22 years ago
In the Spotlight-November 2004almost 22 years ago
Searching for a Viable Business Modelalmost 22 years ago
FDA Moves To Implement New GMP PoliciesAdvertisement
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