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
- 11109 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
why you are become a medical representative
How to do IR test of hydroscopic materials
while formulation of Gliclazide floating tablets why we are using direct cmpression technique why not wet granulation and what happend with that
why didn't you go back to previous employer after shifting to bangalore?
Why SLS used as dissolution medium
what is factor?
How to perform forced degradation on tablet sample or suspensions?
Do you think it is possible to rehabilitate?
what is the mechanism of action of local anaesthetics?
Explain difference between sonication and homozinization?
difference between RF and correction factor?
What is forced degradation study?
What are the regulatory commitments in markets like USA, Canada, Europe, Brazil, South Africa and Japan
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 is the leak test procedure of filled bottles (liquid)
