Found 1,480 presentations matching your search
Change control within a QMS is a formal process used to ensure that a change to a system is introduc...
history of computers m pharm
Medical termination of pregnancy
PRESENTING AND REPORTING IN RESEARCH
Gjjjjhhhjjhhhhjjjjhhgghhhhhhhhjjjhhhhjhh
I'm Mohamed Usman Syed, Pursuing M.Sc, Microbiology at Sri Paramakalyani College, Alwarkurichi -...
The detection of safety signals during clinical trials is a critical component of drug development, ...
Merger and Acquisitions
this slide tells about schedule Y, Good Clinical Practice, CDSCO, Ethics committee, consent form, Se...
#computer #pharmacy #drsiddhiupadhyay #sigmainstituteofpharmacy #preclinicaldevelopment
Product Development & Technology Transfer
Clinical Trial Monitoring as per ICH-GCP E6 R2
Safety pharmacology is a critical discipline that evaluates the potential adverse effects of new pha...
Basics of Clinical Research
An Investigational New Drug Application (IND) is a request from a clinical study sponsor to obtain a...
GxP is a general abbreviation for the "good practice" quality guidelines and regulations. ...
Introduction to Clinical Data Management Process Overview in Pharmaceuticals, Bio-Pharmaceuticals, M...
The interview question series on clinical research is important for several reasons: Assessment of ...
Setting of specification limits as per ICH Q6A
Guidelines By ICH and special emphasis on Quality.
Explanation about quality by design c0ncept
phases of a clinical trial /oncology
The mission of the Clinical Trials Registry-India (CTRI) is to ensure that all clinical trials condu...
