Inside Standards

November 01, 2016

US and Chinese pharmacopeial standards groups commit to collaboration on standards for drug safety.

June 27, 2016

ICH detailed the highlights of the council’s June 2016 meeting.

June 02, 2015

Will biosimilars share a compendial identity like generic drugs do?

March 02, 2015

A General Chapter on mAbs will be published in USP-NF as biologics increase their role in healthcare.

January 15, 2015

USP establishes Jan. 1, 2018 as the implementation date for its elemental impurities guidelines for existing drugs.

January 02, 2015

In late 2014, standards organizations continued to work towards harmonization and securing drug safety.

July 02, 2014

Regulators and industry leaders take on the task of securing the drug supply chain.

June 02, 2014

The European Pharmacopoeia Commission re-evaluates its policy on the development of monographs for finished drug products.

March 02, 2014

USP evaluates quality attributes for synthetic peptides.

February 02, 2014

PDA works with FDA to create pharmaceutical quality metrics.