Join Medidata and LMK Consulting for a Nov. 15 webinar on the future of eTMF (electronic trial master file) management. Learn how Medidata eTMF provides an integrated eTMF solution that’s clean, simple and intuitive.

Hear from Frederico Braga, Medidata Principal of Platform Strategy and Adoption, on the value of eTMF integration and automation; Sholeh Ehdaivand from LMK will present on how Clinical Ops & Clinical IT processes can be improved as a result. Learn how Medidata eTMF manages all your data and content--from study planning to close--on one platform, accelerating study startup and ensuring compliance & inspection readiness. Register today!

Featured Speakers:

Frederico Braga

Principal, Platform Strategy and Adoption
Medidata

Frederico has deep Life Science experience developing and contributing to the implementation of various IDMP and eTMF solutions and has overseen eClinical Programs leading to the implementation of Scientific Computing Environments (SCE), Clinical Data Warehouses (CDW) and Metadata Repositories (MDR). He has lead implementations with a variety of clients including CSL Behring, Grünenthal, Xellia, Alexion, Roche, BMS, Takeda and Johnson & Johnson.

Sholeh Ehdaivand

President and CEO
LMK Clinical Research Consulting

Sholeh is an internationally known TMF Subject Matter Expert with over 15 successful years of experience in the Clinical Research Industry. 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.

NOW AVAILABLE ON-DEMAND

Register now for this webinar