April 8th 2025
Lack of skills in the AI realm was a distant second among those surveyed about the biggest barrier to innovation while using the technology.
Contract service providers must step up their game to stay competitive in increasingly complex bio/pharma market.
Strategies for Early-Stage Drug Development
September 1st 2010Bristol-Myers Squibb's fit-for-purpose mode for clinical-trial materials for early-stage development seeks to achieve a better way in resource allocation. This article is part of a special issue on API Development, Formulation, Synthesis and Manufacturing.
Contract Manufacturing and Continuous Flow Reactor Technology for Early-Stage Drug Development
September 1st 2010The current trend in the pharmaceutical industry for the manufacture of small-molecule therapeutic agents is moving toward continuous flow processes. This article is part of a special issue on APIs.
Managing an outsourced biologics project
September 1st 2010Every biopharmaceutical is unique and products are defined as much by their manufacturing process as their analytical characterisation. Because of this, the development of biologics has many inherent complexities over small molecule projects.
Senate Introduces New Bill on Drug-Manufacturing Quality Standards
August 12th 2010Sen. Michael Bennet (D-CO) introduced a bill earlier this month, the Drug Safety and Accountability Act of 2010, which is designed to improve regulatory oversight of drug-manufacturing facilities and improve related quality standards and monitoring.