OR WAIT null SECS
March 02, 2016
Asking the right questions is crucial to establishing a biopharmaceutical facility design.
The pharma company revealed in a fourth quarter call that it will improve its cell-culture capabilities by focusing on the use of naïve, highly proliferative cells to manufacture its CAR-T drug candidate.
March 01, 2016
The author lists five key areas to consider when selecting a CDMO to develop highly potent formulations.
February 18, 2016
Manufacturing of antibody drug conjugates requires high-containment solutions, such as high-performance aseptic isolators.
The course, intended for healthcare professionals, provides an overview of biosimilar products and FDA’s biosimilar product development programs.
February 11, 2016
Vaccine R&D has grown exponentially in recent years, spurred by ethical and medical needs to combat lethal infectious outbreaks and increased funding from public and private agencies and organizations.
February 09, 2016
There are no clinically meaningful differences between Celltrion’s CT-P13 and Remicade, according to an FDA briefing released ahead of the formal panel meeting.
February 04, 2016
Although switching has occurred in European markets for some biosimilars, most biosimilar manufacturers will focus on securing new users, according to Merck.
ViaCyte and Janssen Biotech have entered Phase I/Phase II clinical trials for VC-01, a candidate treatment for the treatment of type 1 diabetes.
February 02, 2016
Scale-down modeling is instrumental in supporting the development of downstream biopharma manufacturing processes.