OR WAIT null SECS
There is a great need for sensitive, precise, and easily accessible analytical detection techniques for protein sequencing.
The emergence of mRNA vaccines and cell and gene therapies has pushed innovation in analytical methods.
Effective analytics will eliminate failures, deviations, and non-conformances.
February 02, 2012
Where is the variability coming from and what have we done to minimize it?
The Asian nation is strategizing to take the lead over its regional competitors in pharmaceutical exports.
New product reviews for February 2012.
February 01, 2012
In Part I of a three-part article, the authors discuss what constitutes an impurity and the potential sources of impurities in APIs and finished drug products.
January 02, 2012
Technology may expedite operations, but the absence of the human element could cost dearly.
The European Union market takes steps toward continuous processing and modular facilities.
December 21, 2011
PharmTech's monthly newsletter, Equipment and Processing Report, reviews the Editor's Picks for the December 2011 edition from Banner Engineering and Eriez.
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.
December 02, 2011
Cleanliness is crucial, even if zapping and trapping is necessary to reduce product contamination.
The seventh in a series of eight case studies from the Product Quality Research Institute focuses on packout remedies.