OR WAIT null SECS
January 27, 2005
Warning Letter
ISA-88 Automation Standard Gains IEC PAS Status
January 20, 2005
MHRA to Reinspect Chiron Flu Vaccine Plant
January 12, 2005
FDA Warning Letters December 2004
January 07, 2005
NABP Issues Criteria for "Specified List" of Drugs Susceptible to Diversion
January 02, 2005
A swab-sampling method was developed for cleaning validation of a residual active pharmaceutical ingredient in samples collected after cleaning the sampling suite. A summary of the strategies and results of the method development is presented.
Comparative studies of the US Pharmacopeia (645) "Conductivity" and the European Pharmacopeia "Heavy Metals" tests were conducted to demonstrate that the USP method can determine the presence or absence of heavy metals in process water samples.
December 02, 2004
This article provides guidance for developing dissolution testing for poorly soluble compounds. It is the second of a series of articles based on material from a 2003 PhRMA workshop about acceptable analytical practices.
Pharmaceutical Science & Technology News
On the other hand, if we don't keep up the pressure on counterfeiting in the US, we may share the plight of the developing world, where nearly 25% of all drugs sold are fakes.