BioPharm International-07-01-2012

July 01, 2012

A New Era in Cell Culture Media Development

July 01, 2012

Steven S. Kuwahara, PhD, principal consultant at GXP BioTechnology LLC, gives an update on "Engineering the Cell-System Interface."

July 01, 2012

Industry wants more innovation, but can suppliers meet customers' needs?

July 01, 2012

This article contains online-exclusive supplemental material for Malik's article entitled, "Allogenic Versus Autologous Stem-Cell Therapy."

July 01, 2012

Collaborative R&D models coincide with new ways to fund translational research.

July 01, 2012

Unnecessary analytical testing can lead to unnecessary costs.

July 01, 2012

Although FDA cannot do anything to stop drugs from being discontinued, it can do something about supply and quality problems that lead to shortages.

July 01, 2012

The author discusses potential manufacturing costs & challenges of allogeneic & autologous stem-cell therapy.

July 01, 2012

Industry experts discuss methods for optimizing protein expression in bacterial and mammalian cell lines.

July 01, 2012

Selection of the right cell line, culture medium, and bioreactor conditions is key to setting up the upstream portion of the biopharmaceutical manufacturing process.

July 01, 2012

Cell-line specific complex media supplements combine chemically defined media additives into a single supplement.

July 01, 2012

Multiple initiatives are moving forward to maintain US leadership in biopharm R&D.

July 01, 2012

The authors present scale-up from a 5-L fermentor to a 50-L pilot-scale using the criterion of constant power consumption per unit liquid volume.

July 01, 2012

Harmonized regulations call for a risk-based and systematic approach to evaluating and selecting CPPs.