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  Pharmaceutical Technology Europe E-Alert
 
28 May 2013
IN THIS ISSUE
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Featured Topics
Should Regulation of Combination Products Become More Centralized in Europe?
While there are those who want combination products to be controlled by a centralized pharmaceutical-type approval system, the majority of the medical technology industry wants to retain a decentralized device-focused approach. More...
 
Regulatory Roundup
More changes at OGD, FDA budget crunch, and more. More...
 
Regulatory Convergence Sought for Global Pharma Market
Manufacturers work with international authorities to harmonize drug registration and supply-chain oversight. More...
 
 
News
US Government Signs Deal with GSK to Develop Antibiotics
The partnership’s aim is to support the development of drugs to fight antibiotic resistance and bioterrorism. More...
 
Novo Acquires Xellia for $700 Million
Novo A/S, the holding company of Denmark’s Novo Nordisk, has acquired Xellia Pharmaceuticals and purchased all shares of the group for approximately $700 million. More...
 
Pfizer Halts Phase III Trial of Cancer Drug in NHL Due to Futility
Pfizer has discontinued a Phase III study of its investigational cancer drug, inotuzumab ozogamicin, in relapsed or refractory aggressive non-Hodgkin lymphoma (NHL) after it failed to show benefit in overall survival. More...
 
Actavis to Acquire Warner Chilcott
Actavis and Warner Chilcott have entered into a definitive agreement under which Actavis will acquire Warner Chilcott in a stock-for-stock transaction valued at approximately $8.5 billion. More...
 
USP Offers Herbal Medicines Compendium
The US Pharmacopeial Convention is offering free online access to public standards to help ensure the quality of the herbal ingredients used in medicinal products. More...
 
AbbVie and Galapagos Extend GLPG0634 Collaboration
AbbVie and Galapagos have extended their collaboration on the clinical development of GLPG0634 to include Crohn’s disease. More...
 
SCHOTT Introduces Cartridge Design for High-Speed Filling
New design meets new process requirements. More...


Product/Services Profiles
Agilent
Support and Solutions from Agilent for Impurity Profiling: New Genotoxic Impurities Primer
Agilent partners with Pharma for great results. Download or request a hard copy of our new guide, Genotoxic Impurities in Pharmaceutical Products:  Regulations and Analysis, authored by Ludwig Huber. The guide provides specific guidelines for genotoxic impurities and recommendations for implementation according to EMA and FDA guidelines.
Get your copy now
 
Copyright
Webinar: Good Corporate Citizenship and the Respect for Copyright in Life Sciences
In the digital age, your employees share scientific research whenever and wherever they want. But did they ask the rightsholder for permission? Could routine information exchanges in the course of R&D collaboration place your organization at risk? Learn why respecting the copyright of others is the right thing to do for research-driven pharmaceutical companies and increasingly reflects good corporate citizenship.
Join us for a COMPLIMENTARY WEBINAR
 
Keofitt
Keofitt aseptic
The main products for this category is the unique single-use sampling bag systems allowing safe and aseptic sampling from any type of sterilizable sampling valve. Read more

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Upcoming events
World Biotechnology Congress 2013 (3–6 June | USA)
Late Stage Pharma Lifecycle Management (4–5 June | Belgium)
Forum LABO & BIOTECH (4–7 June | France)
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Reference Library

Pharmaceutical Technology Drug Delivery Guides
A three-volume set of drug delivery system handbooks. A compilation of articles on methods and processes of manufacturing and administering pharmaceutical compounds to achieve therapeutic effects. Topics include the development of controlled-release formulations and reformulating injectable drugs for oral delivery ... Click here


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