Found 83 presentations matching your search
Regulatory Requirements For New Drug Approval. This topic is from Industrial Pharmacy-II, B.Pharm Fi...
Biosimilars, its development and it's regulatory guidelines.
bioavailability and bioequivalence
Product Development & Technology Transfer
In Japan, the pharmaceutical industry operates under strict regulatory oversight by the Pharmaceutic...
BA and BE studies. Seminar presented in All India Institute of Medical Sciences (AIIMS - New Delhi)...
SUPAC Guidelines
cadd
Elimination Bioavailability and �Bioequivalence Factors Affecting Renal Excretion or Renal Clearan...
ICH Guidelines were created by The International Council for Harmonization of Technical Requirements...
ICH GUIDELINES IN DETAIL
ICH GUIDELINES STORAGE CONDITIONS
this slide tells about schedule Y, Good Clinical Practice, CDSCO, Ethics committee, consent form, Se...
cross over design,factorial design and equivalence design
This presentation covers the ICH guidelines coding no in details.
Non Clinical Drug Development: Global submission of IND, NDA, ANDA.
PPT
ICH Guidelines of Quality, Safety, Efficacy and Multidisciplinary guidelines that implemented by Int...
505(b)(2) new drug application (NDA) is one of three U.S. Food and Drug Administration (FDA) drug wh...
An Investigational New Drug Application (IND) is a request from a clinical study sponsor to obtain a...
Biosimilars
Nill
clinical trials- definition types of clinical trials various designs of clinical trials such as obse...
clinical trials history and types
