The House Committee on Oversight and Government Reform questioned Heather Bresch during a hearing on the company's decision to raise the price of EpiPen more than 400%. / read more /
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EXPERT INTERVIEW
Francis Flanagan, associate principal scientist at Merck, sat down with Pharmaceutical Technology to discuss using minitablets in pharmaceutical manufacturing.
The agency granted accelerated approval to Sarepta's controversial DMD treatment, under the condition the company conduct additional studies to demonstrate efficacy. / 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
Nanoparticulate technologies are showing promising potential in delivering both small-molecule drugs and biomacromolecules across the blood brain barrier. / 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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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 /
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.
