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BRIEF DESCRIPTION OF VARIOUS TYPES OF DOCUMENTS IN PHARMACEUTICAL INDUSTRY
B PHARMA 6TH SEM PHRAMACEUTICAL QUALITY ASSURANCE Pharmaceutical documentation Need of documentati...
The presentation is about documentation in the pharmaceutical industry. Many important topics are co...
Accenture's StartingPoint Submission Authoring Suite helps pharmaceutical and biotech companies ...
Pharmaceutical Engineering, Are the branch of Pharmaceutics which deals with Some metals and their p...
SlideShare Description: Technology Transfer Related Documents Welcome to SlideShare's collectio...
A dossier refers to a comprehensive collection of documents submitted to a regulatory authority to d...
Pharmacovigilance is the science and activities related to the detection, assessment, understanding,...
Indian Regulatory Requirements: Central Drugs Standard Control Organization (CDSCO). The Central Dru...
CoPP is necessary for exporting medicines and pharmaceutical products from India. The application fo...
#computer #pharmacy #drsiddhiupadhyay #sigmainstituteofpharmacy #preclinicaldevelopment
overview of dossier
it is about dossier filing in India, USA, Europe
In this slide contains SITE ACCEPTANCE TEST IN QUALIFICATION. Presented by: K. SANDHYA RANI (Depart...
Clinical research
Are you planning on opening a pharma company in India and want to get a basic idea? Then yes here yo...
Group presentation
Indian regulatory requirements- CDSCO
Management System is to encourage the: Process of Writing Reviewing Auditing Approving Publishing ...
B. Pharm. Final Year, Sem:- VII, INDUSTRIAL PHARMACY-II, Unit 5, chapter 6:- Indian Regulatory Requ...
Part of validation Process in Pharmaceutical Indistries.
Pharmaceutics
SUPAC
Indian GMP Certification & WHO GMP Certification by Mr. Vishal Shelke https://youtube.com/visha...
