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The Good Clinical Practice (GCP) course is designed to prepare research staff in the conduct of clin...
Special emphasis on Q series guidelines
The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human ...
eMpower Contract Labor Management is an enterprise system which helps organizations in managing th...
ppt on ICH Q7
microorganisms present in raw milk and the sources of milk contamination along with its control.
Pilot plant scale up techniques: General considerations - including significance of personnel requir...
quality control tools, NABL, ISO 9000, ISO 14000 , total quality management, quality by design, ICH ...
Quality assurance ; Pharmaceutical validation
Detailed study of Schedule G,H,M,N,P,T,U, V,X,Y, Part XIIB ,Schedule F&DMR(OA)
THIS IS ABOUT SCHEDULES AND RULES IMPLEMENTED FOR MANUFACTURING, IMPORT, EXPORT, PRESCRIPTION, STOR...
A media fill, also known as an aseptic process simulation, is a critical test used in pharmaceutical...
food quality and assurance
GCP guidelines for clinical research
In this slides contain a ICH guidelines process and information about the organization. https://www....
This topic is included in M.pharm (Pharmaceutical quality assurance) Sub name: quality management sy...
Regulatory Requirements OF REST OF THE WORLD Countries by DIVYA PUSHP
B. Pharm. Final Year, Sem:- VII, INDUSTRIAL PHARMACY-II, Unit 5, chapter 6:- Indian Regulatory Requ...
Concept of Quality, Total Quality Management, Quality by Design, Six Sigma concept, Out of Specifica...
QUALITY MANAGEMENT SYSTEMS (QMS)
The development of therapeutic biologics involves a streamlined approach for their formulation and d...
A detailed study of the organisation and personnel involved in the pharmaceutical industry. These ar...
Elemental impurities and guidelines for impurities and there sources