Interested to Buy Any Domain ? << Click Here >> for more details...
what is meant by CAPA?what is the source for deviation
(unplanned) to occur, though the process developed by
standard validation procedures?
- 3 Answers
- 11154 Views
- GSK GlaxoSmithKline, I also Faced
- E-Mail Answers
Answer Posted / deepika singh, ipqa, navdeep b
Corrective action and preventive action. No process
deviation shall be permitted under standard validation
procedures, but if occur likedeviation in the grade of
active raw material could affect the process parameters and
other critical quality attributes of formulation.
additional testing and revalidation should justify such
deviations
| Is This Answer Correct ? | 2 Yes | 0 No |
Post New Answer View All Answers
What interests you about the position of Medical Librarian in our company?
what is factor?
Can any one tell me that which brand hplc column is used for levetiracetam imp- b test.
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
What are the regulatory commitments in markets like USA, Canada, Europe, Brazil, South Africa and Japan
How to preform dissolution profiling
You will be required to interact with patients. Tell us about your previous experience with patients and how did you deal with the experience.
concomitant administration of 6-mercaptopurine and which product results in severe bonemarrow suppression?
what is meant by artwork review and handling procedure with an example?
Iam a B.PHARMA GRADUATE from DELHI UNIVERSITY and I am looking forward for DRUG INSPECTOR EXAM..kindly mail me any ques papaers reg the same...
If calibration of 12 bowl dissolution apparatus does not meets single stage procedure, how can u proceed calibration?
WHAT IS MEANING OF DEAIATION WITH EXAMPLE
What are your intentions towards the uplift of the hospital.
from hplc chromatogram how can we say that calibration is needed now?
