OR WAIT null SECS
October 02, 2011
The authors describe the concept of the limiting discriminatory the limiting discriminatory threshold (LDT) as an objective means of evaluating the inherent quality requirement of a large-sample content-uniformity test.
September 02, 2011
Might European officials reverse their position on acceptable production methods?
After a series of structural changes, the author wonders whether USP is undergoing an identity crisis. USP CEO Roger L. Williams responds.
September 01, 2011
By providing an information "fingerprint", infrared red spectroscopy is a useful tool for identifying counterfeit pharmaceuticals. The authors identify best practices for ensuring compliance.
USP and the Brazilian National Agency of Sanitary Surveillance are teaming up to develop joint education activities for professionals involved in formulating and using pharmacopeial monograph standards in Brazil.
The author examines sample-preparations methods used in inductively coupled plasma–optimal emission spectroscopy for four test metals.
August 02, 2011
USP promotes horizontal standards for biologics' quality attributes.
June 02, 2011
Ensuring compliance though increased statistical knowledge and resources.
May 18, 2011
How do you assign a minimum sample weight for a US Pharmacopeia balance application when the tested repeatability gives a standard deviation of zero?
May 02, 2011
Regulators and standard-setting bodies are re-examining over-the-counter drugs.