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RAW MATERIALS It is basically the chemical ingredients of a process. starting material, in producti...
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An Investigational New Drug Application (IND) is a request from a clinical study sponsor to obtain a...
GLP for pharmaceutical QC laboratory
validation in pharmacy
It is a graded seminar presentation of Mohammad Abuzar Shaikh Umer on the topic of quality by design...
SUPAC respresents the changes recommended by US FDA at the time of scale up or approval of NDA / AND...
cGMP Training: Deviation handling is important area to reporting and investigation & documentati...
ICH GUIDELINES Q8, QbD
Eisenmenger syndrome is developed in chd when it becomes irreversible
user specification requirements, factory acceptance test, & design qualification is the part of ...
Main regulatory agencies involved in Clinical Trial in nutshell
A presentation outlining the causes of angina, mechanism of action of various anti-anginal drugs, th...
Documented Information
Validation
NSF was founded in 1944 as the National Sanitation Foundation to help standardize sanitation and foo...
GMP and vigilance of pharmacology
Pharmaceutical Validation ( As per M.Pharm 1st sem Syllabus)
Concept of URS,DQ,IQ,OQ,PQ
B.PHARM VI SEM
BPR
Analytical Method Validation is a process that is used to demonstrate the suitability of an analytic...
inotropism - physiology , various inotropes, use of inotropes in anaesthesia and critical care , new...
