looking with QMS section i.e Validation Qualification ,Hold time study , Equipment requalification and IPQA

Looking with QMS section i.e Validation qualification, Process validation and IPQA

Routine IPQA activities.i.e dispensing area ,finished goods storage area to ensure online documentation and cGMP requirements.•Tablet formulation department documentation.•Sampling activity of bulk and finished goods and monitoring of RM & PM.•Reviewing of BMR & BPR .•Performing cleaning validation •Preparation of BMR & BPR . • Issuance of SOP ,Log book  and retrieval.• Compliance of new trial batches. • APQR