We support revamp and upgradation of existing facilities and new projects built to EU GMP, USFDA, PIC/S or WHO requirements, with quality, production and engineering design documentation and validation.
Our team of quality, production, architecture and engineering professionals includes process, mechanical, HVAC, electrical, automation and validation specialists for pharmaceutical, medical device, biotech and food processing facilities.
Quality, production and engineering design review, proposed engineering solution documentation and validation for revamp and upgradation of existing facilities.
Gap Assessment
GMP gap analysis of a facility against current cGMP requirements, to prioritise revamp and optimisation.
Learn more
Engineering Services
Quality, production and engineering design review, solution documentation and validation.
Learn more
Upgradation & Automation
Revamp, retrofitting and upgradation, including 21 CFR Part 11 compliant upgradation projects.
Learn more
2D & 3D Drawing Smart P&ID
2D and 3D models, smart P&IDs and walkthroughs for GMP facilities, equipment and utilities.
Learn more
CQV
Commissioning, qualification and validation for revamp projects.
Learn more
MEP
MEP engineering services and design deliverables.
Learn more
EU GMP, USFDA, PIC/S or WHO compliant new projects: quality, production and engineering design documentation and validation.
Engineering Services
Design documentation and validation for EU GMP, USFDA, PIC/S or WHO compliant new projects.
Learn more
Quality Policy (QMS)
QMS implementation and optimisation, document control, change control, deviations and complaints.
Learn more
MEP
MEP engineering services and design deliverables for new GMP projects.
Learn more
CQV
CQV with risk assessment, following the ISPE baseline guide.
Learn more
2D & 3D Drawing Smart P&ID
2D and 3D models, smart P&IDs and walkthroughs for new facilities.
Learn more
GAMP Services Limited 2026. All Rights Reserved.