Turnkey Projects Consultant in Chennai | Isha’s GMP Consultancy
Isha’s GMP Consultancy — leading turnkey projects consultant in Chennai for pharma & biotech industries. End-to-end design, validation, HVAC, commissioning & documentation.
Overview
Turnkey Projects Consultant in Chennai
As a trusted Turnkey Projects Consultant in Chennai, Isha’s GMP Consultancy specializes in providing complete, regulatory-compliant facility solutions for pharmaceutical, biotechnology, food, and cosmetic industries. With over 15 years of proven expertise, we manage every stage of your project — from concept design to final commissioning — ensuring a seamless handover of a fully operational, GMP-compliant plant.
Our team’s strength lies in setting up cleanrooms, laboratories, HVAC systems, utilities, and quality management systems that meet stringent WHO, EU, and FDA standards. Serving Chennai and major industrial hubs such as Sriperumbudur, Oragadam, and Tambaram, we deliver turnkey solutions that combine engineering precision with regulatory excellence.
Whether you’re establishing a pharmaceutical formulation plant, a biotech R&D lab, or a cosmetic production facility, Isha’s GMP offers tailored turnkey services that ensure efficiency, quality, and compliance — on time and within budget.
Our Turnkey Services in Chennai
We offer complete, end-to-end turnkey consultancy and execution support covering all aspects of project delivery:
- Facility Design & Engineering (GMP, FDA, WHO, EU-compliant)
- HVAC Systems & Clean Room Setup
- Modular Laboratory & R&D Facility Setup
- Pharma, Biotech, Food & Cosmetic Plant Setup
- Mechanical, Electrical & Plumbing (MEP) Works
- Process Equipment Sourcing & Integration
- Automation & SCADA Systems
- Validation & Qualification (DQ, IQ, OQ, PQ)
- Regulatory Compliance & Audit Preparation
- Documentation & Regulatory Filing Support
- GMP Trainings & Quality Management Systems (QMS)
From initial design to commissioning and validation, we deliver turnkey projects that meet both national and international compliance standards, ensuring your facility is audit-ready from day one.
Past Projects in Chennai Region
Case Study 1: Pharma Manufacturing Facility – Sriperumbudur, Chennai
Client: Confidential (Pharma Formulations)
Scope: Complete turnkey execution — design, civil, HVAC, utilities, validation, and documentation.
Outcome: Delivered a 40,000 sq.ft. WHO-GMP compliant plant in 15 months. Facility cleared WHO and FDA audits within the first operational year.
Case Study 2: Biotech R&D Laboratory – Guindy Industrial Estate, Chennai
Client: Biotech Startup
Scope: Modular lab setup with HVAC, process utilities, gas piping, validation, and audit documentation.
Outcome: Delivered a ready-to-operate R&D facility in 5 months, enabling the client to meet early-stage testing and regulatory milestones.
What Our Clients Say
“Isha’s GMP handled every phase — from design to regulatory documentation — with exceptional professionalism. Their team ensured our plant passed WHO-GMP inspection without a single observation.”
– Dr. S. Kumar, Director, Pharma Company, Chennai
“Their turnkey consulting saved us months of coordination. Isha’s GMP team understood our technical needs and delivered a compliant facility well ahead of schedule.”
– Anjali R., Operations Head, Biotech Firm, Sriperumbudur
Frequently Asked Questions (FAQs)
A turnkey projects consultant oversees the entire setup process of a facility — from concept, design, and construction to equipment integration, validation, and documentation — ensuring a ready-to-use, compliant operation.
Depending on project scale, small laboratories can be completed in 3–6 months, while large manufacturing facilities may require 12–18 months
Yes, we provide complete validation services (DQ, IQ, OQ, PQ) and all regulatory documentation for audits, inspections, and filings.
We specialize in pharma (API, formulations), biotech, cosmetics, nutraceuticals, and food & beverage manufacturing.
Absolutely. Our team has guided clients through WHO, EU, USFDA, and MHRA inspections with comprehensive audit preparation and documentation support.