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Development of Generic drug product
Bpharmacy 8 semester pharmaceutical Regulatory science bp804T Unit I New Drug Discovery and develo...
documentation in pharmaceutical industry, master formula record (MFR), DMF (drug master file), distr...
Master formula record, DMF (Drug Master File), Distribution records. Generic drugs product developme...
Biopharmaceutic classification system (BCS) is a substantial part of drug designing and generic prod...
Contents Guidelines for Preparation of Documentation Clinical Study Reports Clinical Trial Monitorin...
Process involved in Generic product development
Regulatory affairs
regulatory affairs
DOCUMENTATION IN PHARMACEUTICAL INDUSTRY, BY Dr. UMESH KUMAR SHARMA
Abbreviated New Drug Application ANDA ppt by Akanksha puri
This comprehensive guide provides a detailed exploration of the ANDA (Abbreviated New Drug Applicati...
Introduction to Dissolution equipment's, Calibration of dissolution apparatus, Dissolution proce...
generic vs branded a comparison for the benefit of the society
The release of the drug substance from the drug product leading to the bioavailability of the drug s...
Pharmaceutical drug approval process regarding NDA and ANDA.
CLINICAL SIGNIFICANCE OF BIOEQUIVALENCE STUDIES, BIOEQUIVALENCE, REASONS TO PERFORM BIOEQUIVALENC...
An Abbreviated New Drug Application (ANDA) contains data which when submitted to FDA's CDER, Off...
A View For Upcoming Drug Discovery
Product Development & Technology Transfer
PPT
M.Pharm 2nd semester
Sishant Rao Divya from BBAU Lucknow
It is applicable for the Generic drugs
![Abbreviated New Drug Application [ANDA]](https://slidepub.com/thumb/5622/63215622.jpg)
