OR WAIT null SECS
February 02, 2013
The US Pharmacopeial Convention contiues to make modernization of standards a top priority in 2013.
January 31, 2013
Two general chapters on elemental impurities? limits and procedures are to become official Feb. 1, 2013, with implementation proposed for May 1, 2014.
January 29, 2013
EMA announces collaboration with Israel, and USP updates chapter on elemental impurities.
January 02, 2013
USP's focus in 2013 involves standards relating to organic impurities, measurement of residual DNA and host-cell proteins in biotechnology products, and elemental impurities.
November 21, 2012
Overt and covert packaging technologies have evolved to authenticate drugs and fight counterfeits.
November 20, 2012
USP announces new drug naming policy and FDA releases two guidance documents.
November 05, 2012
USP revises labeling requirements for Heparin.
November 02, 2012
The US Pharmacopeia's revised General Chapters on elemental impurity limits and testing procedures are set to take effect in December 2012.
The Pharmaceutical Inspection Co-operation Scheme (PIC/S) has finalized a risk-based inspection planning tool for inspectorates to use in applying science- and risk-based principles to planning GMP inspections.
October 16, 2012
New US Pharmacopeial Convention standards provide a universal approach to organizing labels for prescription containers dispensed by US pharmacists in an effort to improve patient understanding.