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DOCUMENTATION IN PHARMACEUTICAL INDUSTRY : WORKING INSTRUCTIONS AND RECORD FORMATS To define specifi...
Main regulatory agencies involved in Clinical Trial in nutshell
B. Pharm. Final Year, Sem:- VII, INDUSTRIAL PHARMACY-II, Unit 4 final chapter 5 Quality management ...
QUALITY MANAGEMENT SYSTEMS (QMS)
Concept of Quality, Total Quality Management, Quality by Design, Six Sigma concept, Out of Specifica...
Slide deck for Pharmacovigilance students/beginners, Healthcare professionals, pharmacists, nurses. ...
hfhurh
Good Laboratory Practice (GLP),Organization for Economic Co-operation and Development(OECD),National...
CLEANROOM
Best practices for people working in cleanrooms: gowning, cleaning, hand spraying, behaviours and as...
Pharmaceutical Regulataory Affairs
A Study on Documentation Maintenance in the Pharmaceutical Industry which includes the main records ...
Current Good Manufacturing Practices (cGMP) form the scientific foundation of pharmaceutical quality...
Food Safety in India
Concept of URS,DQ,IQ,OQ,PQ
STUDY OF VALIDATION PARAMETERS
Introduction, Regulatory requirements for validation, Role of FDA, Code of Federal regulation, Vali...
Concepts of GLP and ISO 9000. The Good Laboratory Practices Guideline (GLP) is an FDA regulation. Go...
BRIEF DESCRIPTION OF VARIOUS TYPES OF DOCUMENTS IN PHARMACEUTICAL INDUSTRY
This is the process that goes into making sure good quality medication is made.
Materiovigilance, Medical device safety, and MvPI (Materiovigilance Programme of India)
#pharmacognosy #drsiddhiupadhyay #sigmainstituteofpharmacy
In this topic , it covers about standard operating procedure in pharmaceutical quality assurance. t...
Use of QA and QC in Pharmaceutical Industries
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