Found 208 presentations matching your search
The safety monitoring in a clinical trail accompanies by common practices in safety monitoring, comm...
This PPT covers the B. Pharm, Pharmaceutical Jurisprudence Unit-I topics with Objectives, Definition...
Development Safety Update Report
LinkedWorld Flow Deck
Pharmaceutical Regulatory Affairs
NEW DRUG APPLICATION AND ABBREVIATED NEW DRUG APPLICATION
Safety Monitoring in Clinical Trails, Safety Proicedures to be Fallowed
This Presentation is an Unit - I of Organizational Design, Change and Development. In this presentat...
Regulatory requirements of BIOAVAILABLITY & BIOEQUIVALENCE STUDIES
Validation is a Science and even the most mundane tasks in healthcare environments, like hand washin...
clinical trials history and types
DRUG DEVELOPMENT
Regulatory writing
New Drug Application (NDA) Filing
Drug development , uses and it's applications, pre clinical trails
505(b)(2) new drug application (NDA) is one of three U.S. Food and Drug Administration (FDA) drug wh...
Indian Accounting Standards
That slides would help students to know about clinical trials, safety of patient/healthy subjects an...
Indian regulatory requirements- CDSCO
Regulatory Requirements For New Drug Approval. This topic is from Industrial Pharmacy-II, B.Pharm Fi...
Describes in detail definition, purpose, participants and goal of good clinical practices (GCP). Giv...
The ppt gives a basic information about ICH-GCP, how it originated , what led to the formation of IC...
Abbreviated New Drug, New Drug Application
