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Turnkey Projects

Greenfield facility development from concept through to an operational, GMP-compliant manufacturing plant.

Concept to Commissioning 15+ cGMP Designs 4+ Regions Served
Overview

One Accountable Partner from Empty Site to First Batch

Turnkey pharmaceutical projects fail at the handovers — between architect and engineer, between contractor and validation team, between commissioning and quality. We hold the whole chain, so GMP requirements are designed in at concept stage rather than retrofitted after construction.

The result is a facility that qualifies first time, because the qualification protocols were written against the design that was actually built.

At a Glance

  • Feasibility studies and master planning
  • Facility design and engineering
  • Construction, commissioning and validation

Need this scoped for your facility and target market? A senior consultant will give you a candid read at no cost.

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Project Components

Six workstreams delivered under a single project structure.

Feasibility & Master Planning

Capacity modelling, site selection, investment case and the GMP master plan that governs the design.

Facility Design & Engineering

Layout, personnel and material flows, cleanroom classification, HVAC, utilities and containment strategy.

Construction & Commissioning

Contractor oversight, construction quality supervision, systems commissioning and turnover documentation.

Regulatory Approval & Validation

Qualification of facility, utilities and equipment, process validation and preparation for authority inspection.

Plant Modifications & Retrofit

Upgrading existing facilities to current GMP standards while maintaining production continuity.

Automation & System Integration

BMS, EMS, SCADA and MES integration with the computerised system validation that follows.

Where We Deliver

Regional experience across four project environments.

  • Europe — EU GMP compliant facility design and qualification for EU market supply.
  • India — Cost-efficient construction with cGMP design standards for regulated export markets.
  • CIS — Facilities designed for PIC/S and national authority requirements.
  • Africa — Greenfield plants and technology transfer supporting local manufacturing initiatives.
Next Step

Ready to Transform Your GxP Strategy?

Book a no-obligation consultation and get practical answers about turnkey projects for your specific product, facility and target market.