Pharmaceutical Technology Europe, Jan 1, 2013 - Pharmaceutical Technology

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PharmTech Europe

Pharmaceutical Technology Europe, Jan 1, 2013
Editor's Comment
Pharma Never Dies
By Adeline Siew, PhD
Happy New Year! It's the beginning of another year in this digital age where science and technology continue to advance with leaps and bounds. And one can't help but ask, what awaits pharma in 2013?
Product Spotlight
Product Spotlight
Editor's Picks of Pharmaceutical Science & Technology Innovations
Aseptic Processing: A Primer
PharmTech speaks to Ray O'Connor from the National Institute for Bioprocessing Research and Training (NIBRT) for an overview of aseptic processing.
Cover Story
A Look Ahead at Manufacturing and Regulation
By Angie Drakulich
FDA talks about the changing scope of regulatory science and its effect on drug reviews, site inspections, overall approaches.
Industry Insider
Manufacturing Misery in Vaccines
By Nathan Jessop
Vaccine manufacturing was predicted in 2008 to be on the cusp of a golden era, but instead the industry has experienced cost pressures, high-profile liability cases and production setbacks.


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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
Breakthrough designations
Protecting the supply chain
Expedited reviews of drug submissions
More stakeholder involvement
View Results
Eric Langerr Outsourcing Outlook Eric LangerTargeting Different Off-Shore Destinations
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerAsymmetric Synthesis Continues to Advance
Jill Wechsler Regulatory Watch Jill Wechsler Data Integrity Key to GMP Compliance
Sean Milmo European Regulatory WatchSean MilmoExtending the Scope of Pharmacovigilance Comes at a Price
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