Found 240 presentations matching your search
This presentation is regarding the rules in hipaa that are implemented by HHS followed by informatio...
The safety monitoring in a clinical trail accompanies by common practices in safety monitoring, comm...
Good Clinical Practice Principle of ICH GCP Institutional Review Board (IRB)/IEC Informed Consent
Project management is a critical aspect of clinical trials, which involves coordinating and managing...
CT
here you can learn details about Preclinicals studies, clinical trails and Pharmacovigilances
clinical trails
These slides re prepared to give the basic knowledge about the planning and execution of clinical tr...
Regarding the Pharmacovigilance safety monitoring in clinical trails
Clinical trails unit for BTech and M.Sc. Chemistry students
Safety Monitoring in Clinical Trails, Safety Proicedures to be Fallowed
Drug development , uses and it's applications, pre clinical trails
Lets, just get to know more about safety reporting in clinical trails with some terminologies, repor...
The New Drug Application is an application submitted to FDA for permission to market a new drug. To ...
This presentation is about the basic responsibilities and functions of CDSCO explaining the regulato...
complete details on clinical studies
Clinical Trial Protocals, Composition of Institutional Ethical Committie, IRB, their functins
which increase the excretion of urine by kidney. They leads to the secretion of excess water and sal...
Clinical trial and types
Bioequivalence studies are conducted to compare the rate and extent of absorption of a generic drug ...
The underrepresentation of minority populations in clinical research has long been a critical issue,...
This presentation gives knowledge on ICH and its History, Mission, and overview of ICH Quality, Safe...
It is unique in bringing together the regulatory authorities and pharmaceutical industry to discuss...
good
