Pharmaceutical Technology Europe, Jan 1, 2012 - Pharmaceutical Technology

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PharmTech Europe

Pharmaceutical Technology Europe, Jan 1, 2012
Editor's Comment
Go UK Bio
By Rich Whitworth
Firstly, Happy New Year! Please help yourself to a slice of cake.
Special Feature
Multilayer Tablets: A Piece Of Cake?
By Marcus Behrens , James Calvin , Doug Kirsch , LakshmiDevi Ethirajan
Multilayer tablets: A piece of cake or just a passing fad? We bring experts together to find out.
Multilayer Tablets: Critical Factors To Consider
By Vilayat A. Sayeed
Multilayer tablets can be challenging, but meeting regulatory expectations is crucial. We speak with Vilayat Sayeed from the FDA, to find out more about the critical factors that need to be fully understood.
Breaking The Mould
By David Beach
PTE interviews Accu-Break's David Beach about using multilayer technology to create accurate breakable tablets and flexible fixed-dose combination drugs.
Fixed-Dose Combinations
By Dr Ajay Gupta , Dr N. Udupa , Dr D. Sreedhar
Fixed-dose combinations (FDCs) reduce the number of pills that must be taken, but they have also been a topic of concern, mainly because of the perceived potential for increased adverse events. PTE speaks with researchers to explore the benefits and concerns of FDCs.
Industry Insider
European Pharma Companies Set To Surge Ahead Of US Rivals
By Nathan Jessop
The next two years may see a shake up in the world's current top pharmaceutical companies, with Pfizer likely to be the only US firm to remain in the top five by sales.
By Stephanie Sutton
The past few years have witnessed some dreary numbers in both Europe and the US when it comes to new products, but 2011 figures released by the European Medicines Agency may be early indicators for a 2012 upturn.


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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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