Turnkey Pharma Projects
From feasibility and plant layout to validation and regulatory approval, we deliver compliant manufacturing facilities on time and within budget.
Turnkey Pharma Projects by Zanax Health
Setting up a pharmaceutical plant involves hundreds of decisions across design, engineering, equipment, utilities and compliance. A single gap can delay approvals by months.
Our turnkey team brings process engineers, GMP consultants and validation specialists together under one contract. We plan, design, procure, install, qualify and hand over a facility that is ready for inspection from day one.
What We Deliver
Feasibility and DPR
Market study, capacity planning, capex estimate and detailed project report.
GMP Layout and Design
Man and material flow, zoning and cleanroom classification as per GMP.
HVAC and Utilities
HVAC, purified water, WFI, compressed air and clean steam systems.
Equipment Procurement
Vendor selection, FAT and SAT for process and packaging lines.
Qualification and Validation
DQ, IQ, OQ, PQ, process validation and cleaning validation.
Audit Readiness
Documentation, SOPs and mock audits before regulatory inspection.
Our Process
Feasibility and DPR
We assess your product mix, capacity and budget to build the business case.
Design and Engineering
Conceptual, basic and detailed engineering aligned to target regulations.
Build and Validate
Construction management, installation and full qualification of systems.
Handover and Audit
Trial batches, documentation handover and inspection support.
Why Clients Choose Us
- Single point accountability from concept to commissioning
- Designs aligned to WHO-GMP, EU-GMP, PIC/S and USFDA
- Optimised capex with phased expansion planning
- Qualified vendor network for equipment and utilities
- Post commissioning training for your team
Frequently Asked Questions
How long does a turnkey project take?
A typical oral solid dosage facility takes 12 to 24 months from design freeze to commercial production, depending on scale, approvals and site readiness.
Do you handle equipment procurement?
Yes. We prepare URS documents, evaluate vendors, attend factory acceptance tests and manage installation and site acceptance.
Can you upgrade an existing facility?
Absolutely. We carry out gap assessments and plan upgrades that bring existing plants up to current GMP expectations with minimal production downtime.
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Explore ServiceReady to Discuss Your Turnkey Pharma Projects Requirement?
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