Found 281 presentations matching your search
Safety pharmacology is a critical discipline that evaluates the potential adverse effects of new pha...
history of computers m pharm
“CSR is a detailed regulatory document which gives the information about the methods and results (...
Quality-by-Design In Pharmaceutical Development: Introduction, ICH Q8 guideline, Regulatory and ind...
A presentation covering QbD inclusive of its definition, goals, advantages, QTTP, Risk Assessment Me...
for the better understanding of the student
regulatory studies
Brief overview of stability testing and its protocol to be followed for stability testing for herbal...
Validation is a Science and even the most mundane tasks in healthcare environments, like hand washin...
Pharmaceutical Quality Assurance B.Pharmacy Third Year Sem- VI As Per PCI syllabus
Concept of SOP in Pharmaceutical organization
Pharmaceutical Manufacturing Technology
Slides prepared for IIUM GCP Workshop
pharmaceutical development report PDR is the one of the significant document of CTD (common technica...
ICH Guideline: Q1A(R2): STABILITY TESTING OF NEW DRUG SUBSTANCES AND PRODUCTS
DABT Study Guide ICH Guidelines M4
Pharmacovigilance is the science and activities related to the detection, assessment, understanding,...
An overview of ICH-GCP guidelines of clinical trials. Good clinical practice (GCP): a standard for t...
ICH Guidelines for stability testing (ICH Q Guidelines)
ICH Q7A means the good manufacturing practice guidance for active pharmaceutical ingredients develop...
Unit-III, Chapter 1. Registration of Indian Products in Overseas Market. B. Pharm. Final Year, Sem-V...
ASEAN COMMON TECHNICAL DOSSIER
clinical research
Bagian RnD industri farmasi berencana mengembangkan sediaan oral Immediate Release untuk dua obat B...
