Found 16 presentations matching your search
Code of Federal Regulations (CFR).CFR is the codification of the general and permanent regulations p...
Prashant Tiwari M. Pharm, Pharmaceutics. Columbia Institute of Pharmacy Raipur, C.G.
Computerized system validation
CGMP guidelines, CFR, CDER and CBER, PIC/S, Environment control in pharma industry, plant layout, ma...
In this slide contains introduction, qualification, preventive maintenance, requalification method. ...
Product Development & Technology Transfer
5. Unit-V- Regulatory Concepts. B. Pharm. Final Year, Sem-VIII, BP804 ET: PHARMACEUTICAL REGULATORY ...
Current Good Manufacturing Practices (cGMP) form the scientific foundation of pharmaceutical quality...
A brief discussion on informed consent process and its implementation in clinical trial.
These specifications are useful for students in pharmacy field
#pharmacognosy #drsiddhiupadhyay #sigmainstituteofpharmacy
OTC drugs (Amended rules) Drug and Cosmetic Act, 1940 & Rules,1945
It's all about the topic of documentation in pharmaceutical industry. In this the specifications...
It deals with the understanding and process for auditing pharmaceutical industries. This covers the...
Manual of clinical microbiology
Farmacologia Básica e Clínica - 13ª Ed.pdf
