OR WAIT null SECS
August 02, 2016
Three-dimensional printing allows unique benefits to be built in to solid-dosage forms.
A Q&A with FDA to gain insight on FDA's views of three-dimensional printing and its regulation in drug manufacturing.
PharmTech’s 2016 survey shows general satisfaction with existing solid-dose and parenteral manufacturing equipment, and slow adoption of continuous manufacturing processes.
June 16, 2016
The agency provides quality, development, manufacturing, and labeling recommendations.
June 02, 2016
This article presents recommendations based on a program that was set up to qualify members of a large, diverse team at one oral solid-dosage-form manufacturing facility.
May 18, 2016
A US government report on advanced manufacturing promotes continuous manufacturing of pharmaceuticals, which has had recent commercial success but faces challenges for widespread adoption.
May 02, 2016
Safe handling of HPAPIs requires determining exposure potential and selecting appro-priate containment strategies.
Armin Gerhardt, associate professor of Pharmaceutical Science, Concordia University Wisconsin School of Pharmacy, discusses the effects of moisture on product quality and how to achieve good control of moisture during pharmaceutical manufacturing operations.
April 12, 2016
FDA approved an update in the manufacturing of Prezista (darunavir) using a continuous manufacturing line at Janssen Supply Chain’s facility in Puerto Rico.