| TOPICAL DRUG FORMULATION |
Jason Carbol, Pia Isabel Tan, Yug Varma, David W. Osborne
Case studies compare efficacy testing of preservatives for topical formulations with probiotic actives.
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| ANALYTICS |
Feliza Mirasol
Stability testing on APIs/finished drug product helps define optimal drug packaging for shelf-life storage.
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| PEER-REVIEWED RESEARCH |
Yurii Pidpruzhnykov, Olena Ruban, Tetiana Kolisnyk
This article describes a new, combined, quantitative method for assessing excipient risks that has been developed by the authors as one possible risk evaluation method.
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| QUALITY |
Susan Haigney
Robert Iser of PAREXEL Consulting answers questions regarding the regulatory expectations of quality agreements and how companies can ensure the quality and safety of their products.
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| LAB OPERATIONS |
Amber Lowry
New and emerging products advance bio/pharma laboratory operations.
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| COLD-CHAIN DISTRIBUTION |
Agnes Shanley
Lower costs, fewer opportunities for temperature excursions, and a smaller carbon footprint are making ocean transport more attractive for pharmaceuticals. Poseidon, a new collaborative pharma initiative, seeks to leverage benefits.
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| EUROPEAN REGULATORY WATCH |
Sean Milmo
The upcoming serialization deadline and the United Kingdom's departure from the European Union could result in supply bottlenecks.
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| US REGULATORY WATCH |
Jill Wechsler
Manufacturers tackle regulatory and competitive issues to develop complex therapies and biosimilars.
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| OUTSOURCING REVIEW |
Ronald A. Rader
Development and adoption of new technologies create challenges that may take years to resolve.
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| ASK THE EXPERT |
Siegfried Schmitt
In-house experts can help select the right systems and suppliers, making validation and compliance easy, says Siegfried Schmitt, principal consultant at PAREXEL.
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