Join us to learn best practices for evaluating and implementing eTMF systems, engaging eTMF users, improving clinical data management, and achieving .. Read more cost savings and workflow efficiencies. As integrated technology permeates every aspect of pharmaceutical, biotech, and medical device clinical trial research it is vital to constantly improve the function of the data processing of your organization. This event will touch upon eTMF user engagement, improving clinical data management, and achieving cost savings and workflow efficiencies. Sholeh is an internationally known TMF Subject Matter Expert with over 15 successful years of experience in the Clinical Research Industry. Her expertise and knowledge in all areas of study management and operational aspects of the clinical trial and document management processes has made her a leader and trusted expert. Her experience includes the TMF Reference Model Subject Matter Expert, eTMF management, domestic and international pharmaceutical and biological clinical trials, clinical trial management, site selection, vendor relations, electronic document management, regulatory submissions, quality control processes and implementation and regulatory inspection preparation and participation. LMK Clinical Research Consulting provides expert solutions and services in quality document management to the life sciences industry.
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