Is it the Validation Policy is a separate document from Validation Master Plan? If yes, could somebody share a sample copy of the VP. or further clarify about this. Thank you.
Yes it is
in general the validation approach is described on the Validation Master Plan but all the Guidelines (FDA21 CFR part 820, EMA eudralex Volume 4 part 1 chapter 1, ICH Q10, ISO 9001) say the Quality System of a Company shall have a quality policy. The Validation Policy is a part of Quality Policy.
I put in order this documentation:
- Manual of Quality
- Site Master File
Regards
3) Validation Master Plan
3i) Validation Plan
All this documents can describe the Validation Policy.