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Contents: European Medicines Agency (EMA) IMPD Introduction Contents of IMPD Objectives Scope Intro...
Aliskiren (Tekturna) is the first orally active renin inhibitor approved for clinical use. It was ap...
The European Medicines Agency (EMA) relies on the results of clinical trials carried out by pharmace...
Various countries around the world have distinct drug regulatory bodies tasked with overseeing the s...
Pharmacovigilance is the science and activities related to the detection, assessment, understanding,...
its about the regulatory agencies all over the world
ICH GUIDELINES Q S E M & REGULATORY REQUIREMENTS OF EU, MHRA, TGA & ROW COUNTRIES
Essential Safety Requirements (ESR) in healthcare refer to a set of criteria and standards that medi...
Project work ppt
In the pharmaceutical industry, API pharmaceutical production is vital for creating high-quality gen...
This slide cover basic aspects , regulatory body and marketing authorisation process in uk and Euro...
Regulatory affairs
it is a presentation about Pharmacovigilance, what is? what is the basic information about it? what ...
What are regulatory bodies:- In the present scenario, pharmaceuticals are considered as the most hig...
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PV history
Nicely described regarding about the overview of ICH guidelines as per PCI syllabus specially for Ph...
Pharmacovigilance
General Introduction of the Central Drugs Standard Control Organization (CDSCO).
'Over-the-Counter (OTC) Medicines' means drugs which are legally allowed to be sold by pharm...
Main regulatory agencies involved in Clinical Trial in nutshell
Regulatory affairs, introduction, History, DRA
Role of all the Government Pharma Regulatory Bodies
![cmc [ chemistry manufacturing control ]](https://slidepub.com/thumb/1133/123501133.jpg)
