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  Pharmaceutical Technology Europe E-Alert
 
7 April 2015
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Featured Content
Europe Strives for a More Efficient Generic-Drug Approval Framework
Proposals to make the decentralized procedure more efficient were discussed at the January 2015 EGA conference. More...
 
USP Publishes Monoclonal Antibody Guidelines
A General Chapter on mAbs will be published in USP-NF as biologics increase their role in healthcare. More...
 
Considering GMPs In Room Design
Cleanability is crucial when choosing components for GMP manufacturing areas. More...
 
Top Stories
NIH Announces Positive Results for Experimental Ebola Vaccine
NIH announced positive safety results from the vaccine, VSV-ZEBOV, and found that all patients in the study experienced a strong antibody response. More...
 
Horizon Offers $1.1 Billion for Hyperion
Horizon Pharma offers to buy Hyperion Therapeutics for $1.1 billion in cash. More...
 
Industry News
GSK Announces US Vaccine R&D Center
GlaxoSmithKline announces global vaccines research and design facility to be based in Rockville, MD, USA. More...
 
Catalent Acquires Australia’s Pharmapak Technologies
Catalent acquires Pharmapak Technologies, a pharmaceutical packaging company based in New South Wales, Australia. More...
 
USP Establishes Elemental Impurities Implementation Dates
USP announces an implementation date of Jan. 1, 2018 for General Chapters <232> Elemental Impurities—Limits and <2232> Elemental Contaminants in Dietary Supplements. More...
 
Merck Joins CAR T-cell Market with $941 Million Intrexon Alliance
Merck Serono announces that it will work with Intrexon to develop a cancer therapy using chimeric antigen receptor T-cells. More...
 
Stronger Pipelines and Approvals Drive Small-Molecule APIs and CMO Opportunities
Statistics presented in a March webinar suggest a strong, but highly fragmented, small-molecule API market.  More...
 
Novartis Inks $250 Million Alliance with Aduro
Novartis announced that it entered into a multiyear alliance with Aduro Biotech to develop cancer immunotherapies, offering up to $250 million in upfront payments and equity investments. More...
 
Hamburg Era Ends at FDA
Commissioner Margaret Hamburg discusses globalization challenges and the need for investment in regulatory science during her last weeks at the agency. More...
 
FDA Denies Amgen's Certification Petition in Biosimilar Patent Dance
Biosimilar applicants will not be required to hand over their biosimilar applications and manufacturing dossiers to innovator companies, determines FDA. More...
 
Webcasts
Best Practices for Effective Environmental Monitoring Program in Bio/Pharmaceutical Production
(On Demand)
Sponsored by SGS Life Science Services
 
Practical Implications of the Lifecycle Approach to API Process Validation
(On Demand)
Sponsored by Regis Technologies Inc.
 
More Webcasts

Product/Service Profiles
DIOSNA Dierks & Söhne GmbH

DIOSNA CCS 10 in Isolator
The advantages of the compact design and ease of use of Diosna's pharmaceutical mixer P1-6 and fluid bed processor Midilab XP are the main reasons for integrating them in isolators when granulation equipment for high potent products at laboratory scale (approx.. 0.1 kg - 5 kg) is needed.
Read more


Reference Library

Pharmaceutical Technology Solid Dosage Combo
Increase your knowledge of solid dosage technology and solid dose tablet manufacturing processes. These comprehensive pharmacology reference guides cover a variety of solid-dosage form principles such as oral solid-dosage forms, powders, mixing and blending, excipients, tableting, and coating. Drug delivery system manufacturing professionals can use the solid dosage manufacturing books to stay current with compressed tablet manufacturing processes, solid dosage processing equipment, tablet-pressing processes, and pharmaceutical industry trends in oral solid dosage manufacturing and solid dosage form development. ... Click here

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