Priyanka chaudhari

Chemical Process Equipment & Pharma Engineering

We provide outsourced compliance documentation support for chemical and pharmaceutical process equipment manufacturers. Our role is to reduce internal QA workload, ensure audit-ready documentation, and support on-time project execution for domestic and export orders.

Scope of Services

Design Qualification (DQ) documentation

Installation & Operational Qualification (IQ / OQ)

Factory & Site Acceptance Test (FAT / SAT) reports

GMP-aligned Risk Assessment (RA)

Equipment documentation dossiers

BOM and instrument list documentation support

All documents are prepared in line with GMP principles and client audit expectations, using structured formats, clear acceptance criteria, and traceable compliance logic.