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TransCelerate BioPharma Inc. Takes Steps Toward Common Clinical Trial Site Qualification & Training
Date:6/20/2013

We look forward to continuing our work with TransCelerate to find other pre-competitive opportunities that will aid the sites, and thereby the industry. It is a true milestone that industry is listening to the sites and taking action like this."

Now that the SQT initiative has achieved these near-term goals, the initiative will move into its second phase, where member companies are continuing to realize efficiencies around pre-qualification efforts such as common oversight measures, training and forms, and assessing the benefits of a common comprehensive framework for investigator/staff and site prequalification.

A list of TransCelerate member companies and their acceptable minimum criteria for GCP training, as well as common forms for investigator CVs and site-specific profile information, can be found at the link under "Site Qualification and Training" here.

About TransCelerate BioPharma Inc.

TransCelerate BioPharma Inc. was formed in 2012 and is a non-profit organization focused on advancing innovation in research and development (R&D), identifying and solving common R&D challenges and further improving patient safety, with the goal of delivering more high quality medicines to patients. TransCelerate evolved from discussions at various forums for executive R&D leadership to discuss relevant issues facing the industry and solutions for addressing common challenges. Founding members include AbbVie, AstraZeneca, Boehringer Ingelheim, Bristol-Myers Squibb, Eli Lilly and Company, GlaxoSmithKline, Johnson & Johnson, Pfizer, the Roche Group, and Sanofi, and all have representation on the Board of Directors. Additional members include Astellas Pharma Inc., Biogen Idec, Braeburn Pharmaceuticals, EMD Serono, Inc. (a subsidiary of Merck KGaA, Darmstadt, Germany), Forest Research Institute (a subsidiary of Forest Laboratories, Inc.) and On
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