Found 127 presentations matching your search
This document describes the detailed information of clinical trial protocol and protocol design. The...
contract research organization
“CSR is a detailed regulatory document which gives the information about the methods and results (...
Presentation providing brief description of clinical trials, their phases, types, Protocol, developm...
Regulatory Affairs
clinical trail documentation
This presentation enumerates the responsibilities of various clinical trial players whilst managing ...
describe about role of sponsor and CRO on clinical trial process
Regulatory writing
Drug development , uses and it's applications, pre clinical trails
ICH GUIDELINE .M.PHARM , B.PHARM REGULATORY AFFAIRS
Seminar on Medical Ethics, presented on 11/02/2018
Requirements And Guidelines For Permission To Import / or Manufacture of New Drugs For Sale or To Un...
#pharmacognosy #drsiddhiupadhyay #sigmainstituteofpharmacy
Schedule y
Japan Regulation Drug Regulatory Affairs
quality control tools, NABL, ISO 9000, ISO 14000 , total quality management, quality by design, ICH ...
The safety monitoring in a clinical trail accompanies by common practices in safety monitoring, comm...
Contract Research Organisations- An Overview in Pharma Field
regulatory affairs
Stability, safety, advertising , labelling and packaging of biologics in EU
Safety Monitoring in Clinical Trails, Safety Proicedures to be Fallowed
Digit HF trial review presentation by a resident
Working on Clinical Trials – Getting started Very few clinical trials are conducted only in one c...
