Interested to Buy Any Domain ? << Click Here >> for more details...
Answer Posted / deepika singh, ipqa navdeep bi
Good Laboratory Practice (GLP) embodies a set of principles
that provides a framework within which laboratory studies
are planned, performed, monitored, recorded, reported and
archived. GLP helps assure regulatory authorities that the
data submitted are a true reflection of the results
obtained during the study and can therefore be relied upon
when making risk/safety assessments.
Good manufacturing practice- is a part of quality system
which ensures that products are consistently produced and
controlled to the quality standards appropriate to their
intended use and as required by the marketing authorization.
| Is This Answer Correct ? | 11 Yes | 0 No |
Post New Answer View All Answers
What is the basic requirement for preparing drug master file , like EDMF , USDMF ?
why you are become a medical representative
please e-mail me the model of Tamil Nadu drug inspector question papers
plz.mail me model papers of drug inspector of chhattisgarh..or MP.if Posible. Mail Id-recha_1428@rediffmail.com...mrs_1428@rediffmail.com,
while formulation of Gliclazide floating tablets why we are using direct cmpression technique why not wet granulation and what happend with that
Tell us about a situation in which you took the extra step for a patient.
Do you think it is possible to rehabilitate?
How are you qualified for the position of Assistant Clinical Director?
What do you mean by GTT? What are the effect of GTT on film coating.
How can I assign a retest date for solvents e.g. toluene, methanol, etc?
when we connect the capacitor banks in series with the circuit? 2 144 pH is having unit?
What r the different sop in or plant
what is meant by artwork review and handling procedure with an example?
what is the mechanism of action of local anaesthetics?
How to perform forced degradation on tablet sample or suspensions?
