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  Pharmaceutical Technology Europe E-Alert
 
24 March 2015
IN THIS ISSUE
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Featured Content
Lyophilization Cycle Optimization of Cell-Derived Products
While the optimization of a lyophilization cycle for a biologic relies on a well-characterized formulation, viscosity and aggregation after product reconstitution must also be carefully managed. More...
 
Implementation of ICH Q3D Elemental Impurities Guideline: Challenges and Opportunities
Assessing risk factors is key to implementing the new ICH Q3D guidelines for elemental impurities. More...
 
CMOs Plan for Capacity Expansions
Is there enough talent to go around? More...
 
 
Top Stories
WHO Joins Forces with ESCMID in the Battle against Global Infections
International day for fighting infection sees European infection specialists advocating vaccines as a viable solution to tackle antimicrobial resistance. More...
 
Recipharm Delivers Serialization Solutions for Abbott in Korea
Recipharm expects to be rolling out further serialization projects during 2015. More...
 
Industry News
Sartorius Stedim Biotech Forms Pact with em-tec to Develop PAT Solutions for Flow Rate Measurements
The new flow sensors, BioPAT Flow, enable precise, reproducible data to be collected on flow rates and mass balances without coming in contact with the medium during measurement. More...
 
Catalent Unveils New Organization to Speed Up Drug Development
Sharon Johnson, senior vice president, Global Quality & Regulatory Affairs, will head the organization. More...
 
Mundipharma Launches Infliximab Biosimilar (Remsima) in Six European Markets
Remsima has demonstrated comparability to the reference product, Remicade, in terms of safety, efficacy, and quality. More...
 
Penn Pharma Adds Contained Roller Compaction Equipment in South Wales
Penn Pharma's equipment addition meets growing need for continuous dry granulation and for handling of highly potent drugs. More...
 
NSF International Publishes National Standard for Excipient Good Manufacturing Practices
NSF's consensus-based standard incorporates multiple regulatory and industry requirements into a single rigorous standard for the manufacturing and distribution of pharmaceutical excipients. More...
 
Valeant Adds $1 Billion to Salix Offer, Amid Bid Battle
Valeant announced that it would increase its original acquisition agreement with Salix to approximately $15.8 billion. More...
 
Kite Pharma Inks Deal to Spur Move into European T-Cell Market
Kite Pharma announced that it acquired T-Cell Factory B.V. in an effort to strengthen its T-cell portfolio. More...
 
Webcasts
Applying Water Activity to Pharmaceutical Technology
March 25, 2015 at 11AM ET
Sponsored by Decagon Devices
 
More Webcasts

Product/Service Profiles

Lucideon

Read Our New Pharmaceutical Newsletter
Download Lucideon's free pharmaceutical newsletter. Learn about our new state-of-the-art quality control testing laboratories and the pharmaceutical chemistry and microbiology services we offer. Meet our experienced team and find out how we can help you. And read about our inorganic controlled release technologies, such as iCRT-deter, an oral drug delivery platform that provides abuse deterrent controlled release. Click here

Podcast
Vetter Development Service Chicago: New manufacturing options tailored to your drug product needs

This podcast showcases Vetterīs capabilities in its Chicago development service site. Additionally, it will inform you about the completed site expansion with the addition of a third cleanroom. Clinical syringe projects are now being accepted at this facility. Learn more
 

Reference Library

Pharmaceutical Technology presents its Analytical Testing Resource Guide combo
A compilation of articles in a three-handbook set covering general Analytical Testing and Stability in the manufacture, packaging, storing, and testing of formulated products.... Click here

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