Concerns have emerged that continued growth in the biosimilars market could be limited by mounting pressure to push down on prescription drug outlays. / read more /
Following the United Kingdom’s decision to leave the European Union, there are two areas that demand attention—clinical trials and marketing authorization. / read more /
Getting the Full Picture Predicting Protein Stability Using Chemical and Thermal Denaturation
Live Webinar: Thursday, September 28 at 11:00 am EDT Register now
Swab recovery parameters are reviewed in detail to define best practices and highlight common mistakes to assure successful recovery studies using a risk-based approach. / read more /
In the pharmaceutical factory of the future, data collected by internet-connected manufacturing equipment improves operational efficiency. / read more /
The media blitz surrounding drug shortages has stopped, but critical medications that have no substitutes remain in short supply. Can new approaches turn this situation around? / read more /
World's first system Fully automated sample preparation module for LC-MS Shimadzu has released a new and unique fully automated sample preparation module (RUO) connected online for LC-MS to the four major clinical research markets in Europe, i.e. Germany, France, Italy and Spain. / Read more/
Date: Exhibition: 4th-6th October, 2016 Pre-Connect Congress : 3rd October 2016 Venue: Fira de Barcelona Gran Via, Barcelona, Spain CPhI Worldwide, the world's leading pharmaceutical platform, co-located together with ICSE, InnoPack, P-MEC and FDF, brings together year on year over 36,000 industry experts from 153 countries around the world to meet and greet, do business and shape the future of the global pharmaceutical industry.
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A three-volume set of drug delivery system handbooks. A compilation of articles related to 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 /
Read feature articles on accelerated scale-up for vaccine production, standards for air cleanliness classification, aseptic filling advances, a flexible approach to cleanroom design, a science-driven approach for microbial control, removing genotoxic impurities, regulatory enforcement, drug shortages, and validation of single-use shipping systems.
