<--- Back to Details
First PageDocument Content
Research / Pharmaceutics / Pharmacology / Pharmaceuticals policy / Clinical Data Management / International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use / Good manufacturing practice / MedDRA / MUT / Clinical research / Pharmaceutical industry / Pharmaceutical sciences
Date: 2012-06-21 12:45:03
Research
Pharmaceutics
Pharmacology
Pharmaceuticals policy
Clinical Data Management
International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use
Good manufacturing practice
MedDRA
MUT
Clinical research
Pharmaceutical industry
Pharmaceutical sciences

REPORT OF THE ICH GLOBAL COOPERATION GROUP

Add to Reading List

Source URL: www.ich.org

Download Document from Source Website

File Size: 64,21 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