Pharmaceutical Technology, Sep 1, 2013 - Pharmaceutical Technology

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PharmTech

Latest Issue
PharmTech Europe

Pharmaceutical Technology, Sep 1, 2013
Featured Content
Gaining Insights on Contract Chemical API Manufacturing
By Patricia Van Arnum
Industry experts share their views on the outsourcing model and the current and future direction of contract chemical API manufacturing.
Optimizing Quality by Design in Bulk Powders and Solid Dosage
By Conrad Winters , Filipe Neves
Case studies on the manufacture of a bluk powder and the development of a tablet show the application of QbD principles.
Coating and Taste Masking with Shellac
By Beverly Schad , Brian Cheng , Eric Van Ness , Tom Riley , Jeff Scholten , Houston Smith
The authors describe the background and applications of fully formulated aqueous shellac for film-coating systems.
Risk Assessment of Excipients
By Patricia Van Arnum
Industry experts share perspectives on risk assessment and mitigation in excipient manufacture and the excipient supply chain.
Making the Best of a Bad CMO-Client Relationship
By Eric Langer
A CMO perspective on the CMO-client partnership.
Examining the Role of Cocrystals in Drug Development and Manufacturing
By Cynthia Challener, PhD
A recent FDA guidance places greater attention on cocrystals as a tool in solid-dosage formulation.
Advancing API Synthesis
By Cynthia Challener, PhD
Commercial-scale amide formation and an improved process route for a tetracycline derivative are some recent developments in API synthesis.

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Survey
FDASIA was signed into law two years ago. Where has the most progress been made in implementation?
Reducing drug shortages
Breakthrough designations
Protecting the supply chain
Expedited reviews of drug submissions
More stakeholder involvement
Reducing drug shortages
70%
Breakthrough designations
4%
Protecting the supply chain
17%
Expedited reviews of drug submissions
2%
More stakeholder involvement
7%
View Results
Eric Langerr Outsourcing Outlook Eric LangerRelationship-building at Top of Mind for Clients
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerRisk Reduction Top Driver for Biopharmaceutical Raw Material Development
Jill Wechsler Regulatory Watch Jill Wechsler Changes and Challenges for Generic Drugs
Faiz Kermaini Industry Insider Faiz KermainiNo Signs of a Slowdown in Mergers
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