Why a Turnkey Project, Not Just Machines
Building or expanding a pharmaceutical facility involves far more than buying equipment. Process design, cleanroom construction, water and HVAC utilities, equipment integration, validation and regulatory documentation must all fit together. When these come from different suppliers, the integration risk — and the blame when something doesn't line up — falls on you.
Buying machines separately
AIPAK turnkey project
Our Turnkey Project Process
Every AIPAK turnkey project follows a structured process — so you always know what stage you are at and what comes next.
Consultation & Requirements
We start from your product, capacity target, market and regulatory requirements, and define the User Requirement Specification (URS).
Concept & Layout Design
Process flow (PFD/P&ID), cleanroom zoning, personnel/material flow and utility load calculation — delivered as a plant layout and 3D concept.
Proposal & Engineering Design
Detailed engineering: equipment specification, cleanroom design, HVAC, water system, and a full project scope aligned to EU-GMP / PIC/S.
Manufacturing & FAT
Equipment is manufactured and tested at our factory; you or your consultant join the Factory Acceptance Test (FAT) before shipment.
Delivery & Logistics
Packing, shipping and customs support to your site, coordinated for the Middle East, Central Asia and other regions.
Installation & Commissioning
Our engineers install and commission the line on site, integrating equipment, cleanroom and utilities.
SAT & Qualification
Site Acceptance Test (SAT), then IQ / OQ / PQ qualification to verify installation, operation and performance.
Training & Hand-over
Operator and maintenance training, complete documentation package hand-over, and support to your first production batches.
After-sales & Support
Ongoing spare parts, remote and on-site support, and assistance for your GMP audits.
From your first enquiry to your first validated batch — one team, one plan, one responsibility.
Why AIPAK as Your Turnkey Partner
One point of responsibility
Process, equipment, cleanroom, utilities and validation under one contract.
Full validation package
URS-to-PQ documentation aligned with PIC/S and EU-GMP — audit-ready.
Engineering depth
Process design, utility calculation and cleanroom (Annex 1) design in-house.
Regional delivery
Experience delivering and installing in the Middle East and Central Asia, with logistics and after-sales support.
Start Your Turnkey Project
Tell us your product, target capacity and market — we'll prepare a preliminary scope and layout proposal.
