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This presentation explains the stages of drug discovery and the clinical evaluation process. It cove...
CARCINOGENICITY
ICH GUIDELINES Q S E M & REGULATORY REQUIREMENTS OF EU, MHRA, TGA & ROW COUNTRIES
This presentation provides a comprehensive overview of Good Clinical Practice (GCP), an internationa...
The given presentation is a short description about OECD GUIDELINES.
DABT Study Guide ICH Guidelines M4
ICH GUIDELINE .M.PHARM , B.PHARM REGULATORY AFFAIRS
Clinical trial and types
A standard for the design, conduct, performance, monitoring, auditing, recording, analyses and repor...
The Slides present guidelines for Acute oral testing of drugs as well as other OECD guidelines in sh...
This presentation will give an idea about basic definition and different types of toxicology.
ICH Guidelines: purpose, participants, process of harmonization, Brief overview of QSEM, with specia...
OECD guidelines for acute and chronic toxicity studies
This presentation will help to understand the principle and purpose of acute dermal toxicity study i...
The guidelines describe about the subacute toxicity studies in rodents with a comparison with the pr...
SINGLE DOSE AND REPEATED DOSE TOXICITY STUDIES: FACTORS AFFECTING SUCH STUDIES AS SPECIES,SEX, ROUTE...
ICH Guidelines of Quality, Safety, Efficacy and Multidisciplinary guidelines that implemented by Int...
Drug development , uses and it's applications, pre clinical trails
INTERNATIONAL CONFERENCE ON HARMONISATION (ICH) E2e GUIDELINES
Pharmacovigilance planning is a systematic approach to ensuring the safety of pharmaceutical product...
M. Pharmacy - Pharmaceutical Regulatory Affairs (MRA) 1st Semester - Regulations and Legislation for...
It is unique in bringing together the regulatory authorities and pharmaceutical industry to discuss...