<--- Back to Details
First PageDocument Content
Pharmaceutical sciences / Center for Biologics Evaluation and Research / Center for Drug Evaluation and Research / Office of Regulatory Affairs / Center for Veterinary Medicine / Biologic / Regulatory affairs / Good Clinical Data Management Practice / Food and Drug Administration / Medicine / Clinical research
Pharmaceutical sciences
Center for Biologics Evaluation and Research
Center for Drug Evaluation and Research
Office of Regulatory Affairs
Center for Veterinary Medicine
Biologic
Regulatory affairs
Good Clinical Data Management Practice
Food and Drug Administration
Medicine
Clinical research

Staff Manual Guide[removed]

Add to Reading List

Source URL: www.fda.gov

Download Document from Source Website

File Size: 23,05 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