Found 29 presentations matching your search
"Introduction to Ethical AI and the Importance of Fairness" explores how artificial intell...
“Building a Better Tomorrow: Data Annotation for Social Impact Projects” highlights the crucial ...
"Data Annotation Techniques: The Foundation of AI" explores how accurate data labeling and...
Non Clinical Drug Development: Global submission of IND, NDA, ANDA.
NEW DRUG APPLICATION INVESTIGATIONAL NEW DRUG ABBREVIATED NEW DRUG APPLICATION
Product Development & Technology Transfer
Pharmacogenetics and Pharmacogenomics
Nill
Basic information for beginners...
The NDA application is the vehicle through which drug sponsors, such as biotech and pharmaceutical c...
505(b)(2) new drug application (NDA) is one of three U.S. Food and Drug Administration (FDA) drug wh...
phases of a clinical trial /oncology
B. Pharm. Final Year, Sem-VIII, BP804 ET: PHARMACEUTICAL REGULATORY SCIENCE (Theory). Unit-I Chapter...
Regulatory Requirements For New Drug Approval. This topic is from Industrial Pharmacy-II, B.Pharm Fi...
A dossier refers to a comprehensive collection of documents submitted to a regulatory authority to d...
Include information about Hatch- waxmann act and amendments, this also include information about pos...
regulatory affairs
Unit-III, Chapter 1. Registration of Indian Products in Overseas Market. B. Pharm. Final Year, Sem-V...
regulation of combination medicine and medical devices
Schedule Y
CLINICAL DATA MANGEMENT (CDM)
In Japan, the pharmaceutical industry operates under strict regulatory oversight by the Pharmaceutic...
Dive into the intersection of Artificial Intelligence (AI), Robotics, and Computational Fluid Dynami...
Technology development and transfer