3 September, 2015. A comprehensive Trial Master File (TMF) requires filing and maintaining hundreds of thousands of clinical documents during clinical trials. This is important both for the patient and for the sponsor companies in order to ensure they are ready for inspection and that GCP guidelines are being followed. As life sciences companies move to semi-virtual environments, keeping only the most vital functions in house, more and more TMFs are being converted to an eTMF format. While implementing eTMF can be costly and training employees can be difficult, it can also ensure real-time monitoring of data. Join our online conference to learn more!
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