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This slide cover basic aspects , regulatory body and marketing authorisation process in uk and Euro...
Analytical method validation is a process of documenting/ proving that an analytical method provides...
In these slides you can get the information of clinical trials which have four phase I,II,III, IV. b...
PCR
about lead identification techniques
Quality by Design Need of QbD Implementation of QbD Analytical QbD Process Analytical Technology GMP...
The Commonwealth of Independent States is a regional intergovernmental organisation, formed in 1991
It describes daily activities of clinical pharmacist
quality by design for formulation and development
An in vitro – in vivo correlation (IVIVC) is defined as a predictive mathematical model describing...
NARGUND COLLEGE OF PHARMACY
Technology transfer (TT) refers to the process of conveying results stemming from scientific and tec...
homeopathic pharmay
Role of pharmacist in hospital pharmacy
Pharmaceutical Validation ( As per M.Pharm 1st sem Syllabus)
Information regarding the regulatory requirements in Rest of the world
presentation on technology transfer in pharmaceutical industry
Rational Chemoprophylaxsis
COMPLAINT HANDLING IN PHARMACEUTICAL COMPANIES,�PRODUCT RECALL,RETENTION RECORDS, DISTRIBUTION RE...
Non-clinical Trials before clinical trials
Review of stability of packaged material like containers and closures. The whole ppt is regarding th...
Regulatory Requirements For New Drug Approval. This topic is from Industrial Pharmacy-II, B.Pharm Fi...
this presentation deals with drug price control in India. it has also updated information on drug pr...
Mallige college of pharmacy
