Despite some progress, pharmaceutical companies have a long way to go in making their products accessible and affordable, this year's study finds. / read more /
A dissolution method should have adequate discriminatory power to detect formulation changes that affect the dissolution rate of a drug product. / read more /
This article will clarify reasonable expectations for the responsibilities of topical product formulation developers and for excipient suppliers regarding the information and samples for experiments needed for QbD. / read more /
A variety of strategies have been employed to deliver proteins and peptides in improved parenteral formulations and/or via noninvasive routes. / read more /
Flexible Manufacturing Solutions
Catalent combines more than 80 years' manufacturing expertise, superior product quality and reliable supply from a global network of over 30 sites for clients around the world. / Read more/
Date: 1 & 2 February 2017 Venue: Paris expo, Porte de Versailles, Paris The event dedicated to the pharma packaging & drug delivery industries.
2017 marks Pharmapack Europe's 20th successful year, and over its lifetime it has grown in size, profile and popularity from a bi-annual event to a major annual show that attracts 5,100+ visitors and over 380 exhibitors from more than 70 countries around the world. / Read more /
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 /
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.
