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September 01, 2011
Direct dosing APIs during R&D studies can reduce the overall testing time of a drug candidate by allowing for a greater throughput of compounds through the R&D department.
The increasing cost of crucial manufacturing input factors, such as energy and raw materials, has been a severe threat to several companies.
As contract manufacturers and fine-chemical suppliers gather for CPhI/ICSE, effective strategies for technology differentiation are key in an increasingly competitive environment.
Recently, there have been many innovations in the latest techniques and technologies in API purification. In particular, the trend to single-use systems has had a significant impact on processes.
March 02, 2011
A new audit guide aims to improve supply-chain security and supplier qualification practice.
December 02, 2010
IPEC extends its reach to Brazil and Argentina in an effort to harmonize excipient best practices.
September 02, 2009
IPEC's new stability testing guide takes into account the full supply chain's storage conditions.
June 01, 2009
Today, approximately 1.5 million counterfeit medicine packs enter the legal supply chain each year - in other words, one pack in every 20000 is counterfeit.
May 02, 2009
The GDP committee of IPEC–Europe is trying to seal one more broken link in the supply chain. This article contains bonus online-exclusive material.
February 02, 2009
Without any GMP guidelines for excipients in Europe, change can't come soon enough for some industry groups.