End-to-End Solutions
Turnkey Manufacturing Project Solutions
From a blank site to a fully licensed, production-ready manufacturing facility — IMEX manages every phase so you don't have to coordinate multiple agencies.
50+
Turnkey Projects
100%
On-Time Delivery
15+
Years Experience
20+
States Pan-India
Our Process
How We Deliver Your Facility
Feasibility & Planning
- Regulatory feasibility assessment
- Site selection guidance
- Project scope definition
- Budget and timeline planning
Design & Engineering
- Plant layout and flow design
- GMP-compliant architectural plans
- HVAC and utility system design
- Equipment selection and specification
Construction & Setup
- Civil construction oversight
- Equipment procurement and installation
- Utility commissioning
- Clean room qualification
Validation & Licensing
- IQ / OQ / PQ validation protocols
- Schedule M compliance documentation
- License application and submission
- Regulatory inspection support
Sectors We Serve
Turnkey Solutions Across Manufacturing Categories
Pharmaceutical Manufacturing Units
Greenfield and brownfield pharmaceutical plants — oral solids, liquids, injectables, and topicals — designed and licensed to Schedule M GMP standards.
Cosmetics Manufacturing Facilities
Complete setup for skincare, haircare, and personal care product manufacturing — from plant design to BIS certification and State FDA licensing.
Nutraceutical & Food Supplement Plants
FSSAI-compliant manufacturing units for health supplements, nutraceuticals, and functional foods — designed for both domestic and export markets.
Ayurvedic & Herbal Manufacturing
Traditional medicine manufacturing units compliant with AYUSH guidelines — from raw material processing to finished product licensing.
WHO-GMP Compliant Facilities
Pharmaceutical manufacturing facilities designed and qualified to WHO-GMP standards — supporting international regulatory approvals and export market readiness.
International Standards
WHO-GMP Consultancy Services
IMEX provides comprehensive WHO-GMP compliance consultancy for pharmaceutical manufacturing facilities — from gap assessment and QMS development to inspection readiness and international audit preparation.
WHO-GMP Gap Assessment
- Comprehensive facility evaluation against WHO-GMP requirements
- Identification of critical, major & minor compliance gaps
- Detailed gap analysis report with corrective action recommendations
- Risk-based compliance assessment
Audit Readiness & Inspection Support
- Pre-audit and mock inspections
- Inspection preparedness programs
- Documentation review and compliance verification
- Audit response strategy and CAPA implementation
Quality Management System (QMS)
- Quality Manual preparation
- SOP development and review
- Deviation, Change Control, CAPA & Risk Management systems
- Data Integrity compliance and document control
Facility & Engineering Compliance
- Facility design and layout review
- HVAC system qualification support
- Water System Validation (PW, WFI)
- Cleanroom qualification and environmental monitoring
- Equipment Qualification (DQ, IQ, OQ, PQ)
Validation & Qualification
- Process, Cleaning & Analytical Method Validation
- Computer System Validation
- Qualification Master Plan preparation
- Validation Protocols and Reports
Production & QC Compliance
- BMR and BPR review
- Laboratory compliance assessment
- Stability study program evaluation
- OOS, OOT and laboratory investigation systems
- Reference standard and reagent management
Manufacturing Facilities Covered
- Tablets and Capsules
- Oral Liquids and Syrups
- Dry Syrups
- Ointments, Creams and Gels
- Sterile Products
- Injectables
- Ophthalmic Preparations
- Veterinary Products
- Nutraceuticals & Supplements
- Medical Devices
- Cosmetics Manufacturing
- External Preparations
Training & Capacity Building
- WHO-GMP awareness programs
- GMP training for production personnel
- QA and QC training
- Data Integrity training
- Inspection readiness workshops
Key Benefits
- Improved GMP Compliance
- Enhanced Product Quality Systems
- Increased Regulatory Confidence
- Better Inspection Outcomes
- Global Market Readiness
- Sustainable Quality Culture
Why Choose IMEX
The Turnkey Advantage
- Single-point accountability from concept to commissioning
- In-house regulatory team ensures compliance from day one
- Established vendor network for equipment and construction
- Parallel processing of construction and licensing timelines
- Post-commissioning compliance support included
- Experience across 50+ turnkey projects pan-India
Start Your Project
Tell us about your manufacturing vision and we'll provide a free feasibility assessment.