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Platform Technologies
March 2, 2012
By:
Erik Greb
,
Angie Drakulich
The standardization of upstream and downstream bioprocessing is growing, but several kinks need to be ironed out.
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Robots' Role in Flexible Fill–Finish Lines
January 18, 2012
By:
Erik Greb
The pharmaceutical industry has a history of developing innovative medicines and novel drug-delivery systems, but not all of its manufacturing processes use cutting-edge technologies. Demands to increase productivity in fill–finish lines are fueling the arguments of proponents of robotic automation to expedite manufacturing.
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Ranbaxy Signs Consent Decree with FDA
December 29, 2011
By:
Erik Greb
On Dec. 21, 2011, Ranbaxy Laboratories signed a consent decree with FDA and pledged that it would strengthen procedures and policies to ensure data integrity and to comply with current good manufacturing practices. The agreement is subject to approval by the US District Court for the District of Maryland.
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Baxter and Momenta to Develop Follow-On Biologics
December 29, 2011
By:
Erik Greb
Last week, Baxter International and Momenta Pharmaceuticals entered into a global collaboration to develop and commercialize follow-on biologic products. The two companies expect to close the transaction during the first quarter of 2012, subject to customary closing conditions.
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HHS and Novartis Dedicate First Cell-Based Flu Vaccine Plant in US
December 22, 2011
By:
Erik Greb
Last week, the US Department of Health and Human Services and Novartis Vaccines and Diagnostics dedicated a manufacturing plant that can create influenza vaccine using cultured animal cells instead of the conventional expression system of fertilized eggs.
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Moving from a Reactive to a Systemic Approach to Manage Risk
December 21, 2011
By:
Erik Greb
Risk assessment is not a new concept to the pharmaceutical industry, but lately the phrase has become a mantra. A systemic, science-based way to manage risk is becoming essential to meeting the spirit and letter of FDA requirements.
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FDA Warns Novartis of Violations at Three Plants
December 15, 2011
By:
Erik Greb
In a Warning Letter, FDA cited "significant violations" of CGMP regulations, including several repeat observations, at three Novartis facilities located in Colorado, North Carolina, and Canada.
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PhRMA Foundation Funds Comparative-Effectiveness Research
December 8, 2011
By:
Erik Greb
Last week, the Pharmaceutical Research and Manufacturers of America Foundation awarded Johns Hopkins University and the University of Washington each a $250,000 grant to establish a three-year graduate certificate program. The program is formally known as the PhRMA Foundation Center of Excellence for a Comparative-Effectiveness Research Educational Program. The funds are the foundation's first grants to educational institutions.
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