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Top Stories
Roche launched imCORE, a global network of cancer immunotherapy centers of excellence.
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Nine fellows recognized for research ranging from cancer treatment to improved vaccines.
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Industry News
AAPS presents Dale E. Wurster award to Stephen Byrn for his work in the field of solid state chemistry.
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The Broad Institute and IBM Watson Health will collaborate on a $50 million project to study how cancers become resistant to therapies.
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PODCAST
Jennifer Zieverink, senior director of marketing and alliance management at Aprecia, and Grant Brock, vice-president of engineering at Aprecia, spoke with Pharmaceutical Technology about the company's ZipDose Technology, which is a three-dimensional printing technology used to make solid-dosage drugs.
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Take charge of your tablet design with Natoli Engineering's TabletCAD. This free web-based software allows you to design shapes, derive punch tip force and total volume, generate drawing to share with colleagues and more! TabletCAD is a simple, cost-effective way for you to create tablets to your organization's specifications. Join the growing number of manufacturers who are designing their tablets in the cloud.
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Supplier News
The new Boston laboratory offers advanced analytical testing services.
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Dedicated facility will address enhanced regulation of metals and impurities in pharmaceuticals.
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Bio/Pharma News
The agreement allows Bristol-Myers Squibb exclusive license to manufacture and commercialize Nitto Denko Corporation's NASH treatment.
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The study in 48 healthy adults will assess the safety and immunogenicity of a prime-boost regime of two different intranasal doses of the RSV vaccine, SynGem.
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Guidelines and Regulations for cGMP Mapping
There are 5 different guiding and regulating agencies for cGMP mapping processes. This document summarizes the agencies and the specific articles that should govern your mapping project in warehouses, production facilities, rooms and chambers.  Download the document (PDF file). |
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Regulatory News
The agency recommended nine drugs including treatments for diabetes, hepatitis B, and HIV.
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FORMULATION
A dissolution method should have adequate discriminatory power to detect formulation changes that affect the dissolution rate of a drug product.
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PEER-REVIEWED RESEARCH
This article will clarify reasonable expectations for the responsibilities of topical product formulation developers and for excipient suppliers regarding the information and samples for experiments needed for QbD.
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DRUG DELIVERY
A variety of strategies have been employed to deliver proteins and peptides in improved parenteral formulations and/or via noninvasive routes.
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Events
December 7–8, 2016
January 9–13, 2017
May 16–18, 2017
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REFERENCE BOOKS |
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Increase your knowledge of solid dosage technology and solid dose tablet manufacturing processes. These comprehensive pharmacology reference guides cover a variety of solid-dosage form principles such as oral solid-dosage forms, powders, mixing and blending, excipients, tableting, and coating. Drug delivery system manufacturing professionals can use the solid dosage manufacturing books to stay current with compressed tablet manufacturing processes, solid dosage processing equipment, tablet-pressing processes, and pharmaceutical industry trends in oral solid dosage manufacturing and solid dosage form development.
/ Click here /
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eBOOKS
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Read feature articles on accelerated scale-up for vaccine production, standards for air cleanliness classification, aseptic filling advances, a flexible approach to cleanroom design, a science-driven approach for microbial control, removing genotoxic impurities, regulatory enforcement, drug shortages, and validation of single-use shipping systems. |
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