<--- Back to Details
First PageDocument Content
Clinical research / Pharmaceutical industry / Clinical trials / Design of experiments / Food and Drug Administration / Contract research organization / Institutional review board / Case report form / Investigational device exemption / Site management organization / Clinical research coordinator / Monitoring in clinical trials
Date: 2015-12-14 16:21:29
Clinical research
Pharmaceutical industry
Clinical trials
Design of experiments
Food and Drug Administration
Contract research organization
Institutional review board
Case report form
Investigational device exemption
Site management organization
Clinical research coordinator
Monitoring in clinical trials

Microsoft Word - MAGI_Model_CTA v1.07 Abbreviated.doc

Add to Reading List

Source URL: magiworld.org

Download Document from Source Website

File Size: 152,00 KB

Share Document on Facebook

Similar Documents

The EVMS Autism Spectrum Disorder Program was started by Maria Urbano, M.D., and Kathrin Hartmann, Ph.D., in 2010 to provide clinical services, research, and community outreach to individuals and their families for Autis

DocID: 1vrwY - View Document

Towards a Composite Clinical Endpoint: Identifying a Core Set of Patient and Caregiver Relevant Outcome Measures Through Qualitative Research on the Global Impact of Dravet Syndrome Rima Nabbout1, Stephane Auvin2, Cather

DocID: 1vpIt - View Document

Clinical Research Registration at Public Registry

DocID: 1vnxr - View Document

Grattoni Alessandro, Ph.D. Chairman, The Department of Nanomedicine, The Houston Methodist Research Institute, Houston, Texas (USA) Dr. Grattoni’s research is dedicated to the development and clinical translation of im

DocID: 1vi9N - View Document

Clinical & Translational Research 101 Thursday, August 10, 2017 Time Location

DocID: 1vglz - View Document