Found 26 presentations matching your search
This presentation gives a brief knowledge of CIOMS, its history, missions and collaborations of CIOM...
CIOMS
CIOMS and applications
AEFI
Regulatory Affairs
Regulatory reporting is a fundamental aspect of scientific research and is crucial for ensuring comp...
THIS IS ICH E2A GUIDELINE -CLINICAL SAFETY DATA MANAGEMENT: �DEFINITIONS AND STANDARDS FOR �EXPE...
pharmacovigilance in INDIA,US,EUROPEAN UNION
Providing Submissions in Electronic Format — Post marketing Safety Reports
MedDRA is a terminology used in pharmacovigilance which is used in coding the different aspects in c...
The safety monitoring in a clinical trail accompanies by common practices in safety monitoring, comm...
This presentation points out the various guidelines laid out by World health organization for safe &...
Safety Monitoring in Clinical Trails, Safety Proicedures to be Fallowed
Introduction to Drug Safety & Pharmacovigilance Process Work Flow for Pharmaceuticals, Bio-Pharm...
An Adverse event following immunization (AEFI) is any untoward medical occurrence or event which fol...
An overview of international and Indian ethical codes for conducting research on human subjects
institutional ethics committee
UNIT-2-CODE OF CONDUCT.pptxUNIT-2-CODE OF CONDUCT.pptxUNIT-2-CODE OF CONDUCT.pptxUNIT-2-CODE OF COND...
CME on Pharmacovigilance at NIA
Pharmacovigilance
chap 3- principles of H.E for HEW.pptx
Here is a detailed description of ICH guidelines for PBRER (ICH E2C R2) & Expedited reporting (E...
