OR WAIT null SECS
Advancements in personalized medicine and other innovations are transforming the way dosage forms are viewed.
This study aimed to develop a taste-masked drug resin complex using the ion exchange resin Kyron T-114.
Novel genetic engineering technologies are transforming the design and manufacture of bispecific antibodies, which are emerging as a promising new class of biologics.
January 05, 2016
Ionis Pharmaceuticals receives orphan drug designation for HTTRx for the treatment of Huntington’s disease.
January 04, 2016
BioPharm highlights the monoclonal antibodies that may gain United States regulatory approval in 2016.
January 02, 2016
Parenteral packaging of the future will include more automated lines, ready-to-fill packaging formats, and supply-chain transparency.
Infrastructure and payer decisions will determine drug choices in emerging and developed regions.
Amid corporate restructurings, regulatory initiatives, and aging R&D assets, will drug development accelerate or stall in 2016?
FDA approved 45 novel new drugs in 2015, the highest number of approvals since 1996 and second-highest ever.
Regulatory, corporate restructuring, and manufacturing issues will challenge bio/pharma to meet the needs and expectations of patients around the world.
January 01, 2016
Liquid formulations in hard-shell capsules or softgels are becoming a popular option for HPAPIs because of advantages such as improved safety and lower risk of potential exposure and product cross contamination.
The DF30Plus, a new version of Aptar Pharma’s aerosol metering valve for pressurized metered dose inhalers (pMDIs), incorporates an elastomeric cyclic-olefin-copolymer (COC) neck gasket.
Synthetic biology promises to drive tomorrow’s therapies, while continuous processing is already being used in some new drugs.