Validation Protocol

Avenue Mould’s┬ásignificant expertise in validation (IQ,OQ & PQ), Class 8 (100,000) clean room and in-depth knowledge of regulatory requirements has earned us a reputation for excellence among our customer base.

Our capabilities include in-house protocol generation, with validations also carried out to customer supplied protocols.

In both instances all validation protocols and reports are sufficiently comprehensive to meet FDA (code of Federal Regulations, 21CFR, part 820) and Global Harmonisation Task Force (GHTF) Process Validation Guidance.