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
from hplc chromatogram how can we say that calibration is needed now?
Can any one tell me that which brand hplc column is used for levetiracetam imp- b test.
What r the different sop in or plant
You will be required to interact with patients. Tell us about your previous experience with patients and how did you deal with the experience.
How are you qualified for the position of Assistant Clinical Director?
concomitant administration of 6-mercaptopurine and which product results in severe bonemarrow suppression?
plz.mail me model papers of drug inspector of chhattisgarh..or MP.if Posible. Mail Id-recha_1428@rediffmail.com...mrs_1428@rediffmail.com,
What are your intentions towards the uplift of the hospital.
Anyone have any idea when to conduct Uniformity of Weight (UOW) and when need to conduct Uniformity of Dosage Units (UOD) or when need both? I read BP it only said if average weight < or = 0.04g then just conduct UOD, no need UOW. Under UOD section, it doesnt say when need to conduct UOD but just said UOD got two type, one is Mass Variation (MV), another is Content Uniformity (CU) and under what conditions to conduct them. For USP, no UOW section, only got UOD section.
What was your most difficult experience with this population and how did you deal with it?
Give an example of how you've handled a problem patient.
what is meant by artwork review and handling procedure with an example?
What is difference between Warm and Lukewarm Water as per pharmacopia.
What is the basic requirement for preparing drug master file , like EDMF , USDMF ?
How to do IR test of hydroscopic materials