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
Why SLS used as dissolution medium
what is factor?
Tell us about a time when you failed to meet a deadline. What were the repercussions?
What skills have you acquired that would apply to the position of Clinical Data Manager?
What are your intentions towards the uplift of the hospital.
How can I assign a retest date for solvents e.g. toluene, methanol, etc?
What r the different sop in or plant
What is the basic requirement for preparing drug master file , like EDMF , USDMF ?
What are the filing requirements for ANDA-USA, Europe, Brazil, South Africa, Japan and Emerging Markets
why nitrogen charecter as a inert gas plz identified
from hplc chromatogram how can we say that calibration is needed now?
what is the leak test procedure of filled bottles (liquid)
when i come in contact with any metal items or clothes of fur i find myself shock and when run my fingers on fur clothes or matters, i find sparks. Is there any vitiams deffecieny in my body. If so, what i have to do?
WHAT IS MEANING OF DEAIATION WITH EXAMPLE
How to preform dissolution profiling
