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Medpace

Medpace, a global full-service clinical research organization, provides Phase I-IV core development services for biopharmaceutical and device programs. Medical and regulatory expertise in multiple therapeutic specialties allows Medpace to conduct strategically integrated studies for sponsors - executing at all levels - providing complete and seamless global drug development services.

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Locations

Africa
APAC
Australia
Europe
North America
South America

Overview Accreditations / Enablement

Therapeutic Areas

Cardiovascular
Devices and Diagnostics
Endocrinology
Hematology
Immunology
Infectious Diseases
Metabolic Diseases
Nephrology
Neurology
Oncology
Other
Psychiatry
Rare Disease
Vaccines

Accreditations / Enablement

Partners are trained on the functionality of the Coder application, process optimization, and scope of Coder services. This Accreditation teaches Partners to integrate the medical coding solution with EDC studies and administer Coder segments. Coder Accreditation is dependent on the successful completion of the Rave EDC accreditation.

Partners are trained on the functionality of the electronic data capture (EDC) and clinical data management (CDM) system, process optimization exercises and scope of Medidata Rave services. This Accreditation teaches the staff to perform end user training, user and site administration, study build, reporting, outputs and amendment manager.

Partners are trained on the functionality of the targeted source document verification (TSDV) application, process optimization, and scope of TSDV services. This Accreditation teaches Partners to implement TSDV in line with regulatory compliance and data quality strategies. TSDV Accreditation is dependent on the successful completion of the Rave EDC Accreditation.

Partners are trained on the functionality and administration of Site Cloud: End of Study content distribution. This includes study and site access provisioning, site content download, and electronic signature acknowledgement. This Accreditation teaches the Partner to administer the electronic distribution and management of study files to sites, including the centralized collection of acknowledgement of receipt documents following delivery.