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  Pharmaceutical Technology Europe E-Alert
 
9 July 2013
IN THIS ISSUE
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Featured Topics
Europe Calls for Guarantee of GMP Standards
Falsified Medicines Directive requires imported APIs to have written confirmation of GMP standards. More...
 
FDA Creates Programs to Expedite Drug Development
Programs assist in the fast track of drugs for serious conditions. More...
 
Public Perceptions of Clinical Research Improves
A study shows significant improvement in public perceptions of clinical trial safety, trust in the motives of research professionals, and appreciation for trial volunteers. More...
 
Croatia Joins European Medicines Network
Europe prepares for inclusion of Croatia in EMA activities. More...
 
Industry News
Seattle Genetics Forms ADC Pact with Bayer
Seattle Genetics could potentially receive approximately $500 million in fees, milestones and royalties. More...
 
Aspen to Acquire Select API Assets and Finished Products from Merck
The $1-billion deal includes select parts of Merck’s manufacturing site in Oss, The Netherlands and Sioux City, Iowa as well as 11 finished products. More...
 
Onyx Rejects Amgen’s Unsolicited Acquisition Bid
The Onyx board of directors rejects $120-per-share proposal as significantly undervaluing the company. More...
 
MorphoSys and Celgene Sign Monoclonal Antibody Pact
The companies agree to jointly develop and promote MOR202, an oncology mAb in a deal potentially valued at more than $800 million. More...
 
Roche, AstraZeneca Partner in Medicinal Chemistry
Companies hope the collaboration will result in identifying potential new drug candidates using fewer rounds of design, synthesis, and testing. More...
 
Almac Adds Contained Drug Handling and Bottling Capabilities
Almac introduces handling and bottling capabilities in EU and US headquarters. More...
 
Xencor Partners with Merck in Antibody Technology
The partnership provides access to Xencor’s Fc engineering patents for monoclonal antibodies. More...
 
WIL Research Acquires Ricerca’s Pharma Service Business in Lyon, France
The move doubles the CRO’s capacity in Europe. More...
 
Hermes Pharma Completes FDA Inspection
Hermes Pharma announced that the company completed a successful inspection by the US FDA of its production facility located in Wolfratshausen, Germany. More...
 
Webcasts
Integrated Solutions for Maintaining Product Quality without Sacrificing Titer
Wednesday, July 17, 2013 at 11:00 AM EDT
Sponsored by Life Technologies
 
Overcoming Challenges in Development of Oral Enteric and Controlled-Release Dosage Forms
Thursday, July 18, 2013 at 11:00 AM EDT
Sponsored by Patheon
 
More Webcasts

Products/Services Profiles
Agilent
Do More Together with Open Access Solutions
Agilent’s open access solutions enable pharmaceutical scientists to accelerate discovery by simplifying the management of multiple LC/MS and NMR instruments.  New MassHunter Walkup Software allows analytical chemists to easily configure and maintain multiple MS instruments, spending more time doing other work.  New Vnmr J 4 Persona Manager provides NMR facility managers with a flexible platform for managing multiple users and spectrometers.  Attend a webinar. www.agilent.com/chem/togetherpharma#openaccess
 
Catalent Pharma Solutions
Catalent’s OSDrC® OptiDose™ enables the design of dividable, multi-layer, single or multi-core tablets with a practically endless variety of core numbers, shapes, sizes, and placement within the tablet.Read More
 
Colder Products Company
Colder’s new genderless AseptiQuik® G Connectors make single-use sterile connections faster, easier and safer—even in non-sterile conditions. Universal mating simplifies systems integration, increases process flexibility and minimizes operator error.Read More
 
Agilent
Agilent’s open access solutions enable pharmaceutical scientists to accelerate discovery by simplifying the management of multiple LC/MS and NMR instruments.Read More

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Reference Library

Pharmaceutical Technology presents its Process Analytical Technology resource guide combo
A compilation of informative, useful articles designed to help you meet the challenges of process analytical technology, become more efficient in testing, reduce over-processing, enhance consistency, and minimize rejects ... Click here


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