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Turnkey projects

Greenfield Pharma Project Solutions by Univita – From Concept to Fully Operational Facility
Univita is a trusted provider in Europe, India, CIS & Africa offering fully integrated solutions for Greenfield project development.
With a strong focus on the pharmaceutical industry, we deliver complete project lifecycle support—covering everything from initial idea generation, planning, and design through to execution and final commissioning.
Whether you are establishing a new Greenfield pharmaceutical venture or developing a modern manufacturing unit, our expert team ensures a smooth, well-coordinated journey from concept stage to full-scale production.

What Does a Pharmaceutical Greenfield Project Mean?

A pharmaceutical Greenfield project involves creating an entirely new production facility on untouched land, built completely from the beginning. Unlike brownfield projects that focus on renovating or expanding existing plants, Greenfield developments are constructed on vacant sites, offering complete freedom in design and execution. This approach enables highly tailored facility planning, improved operational flow, and easier alignment with regulatory standards.

With Univita’s Greenfield engineering expertise, you gain access to:

  • Capacity calculation & Business plan preparation
  • Facilities specifically engineered for maximum operational efficiency
  • Smart layout planning that enhances process and material movement
  • Adherence to both national and global GMP requirements
  • Scalable infrastructure designed to support long-term growth

Why Select Univita for Greenfield Projects?

Strong Expertise Across Pharmaceutical Segments

With extensive experience in Greenfield plant development, Univita delivers customized solutions for a wide range of operations including APIs, finished dosage forms, biotechnology units, and sterile manufacturing facilities.

GMP-Driven Facility Engineering

Our approach is fully aligned with GMP principles, ensuring compliance with global regulatory authorities such as FDA, WHO, EU, and PIC/S. As a trusted name for GMP service support, we have consistently helped clients achieve successful audits with no major observations.

Comprehensive Greenfield Project Support

Univita provide complete, structured assistance across every stage of Greenfield facility development, including: 

  • Feasibility and viability assessment
  • Master planning of the site
  • Detailed plant layout engineering
  • Utility system planning and design
  • HVAC systems, water systems, and cleanroom solutions
  • Construction supervision and commissioning
  • Regulatory approvals and validation support

Regulatory Compliance Built Into Every Phase

Being a provider of GMP services in Europe, CIS, India and Africa, we integrate compliance directly into project execution. Every stage of development is aligned with global regulatory expectations such as:
  • Current Good Manufacturing Practices (cGMP)
  • WHO-GMP standards
  • USFDA requirements
  • EU GMP guidelines
  • MHRA and other international regulatory frameworks
This ensures your facility is fully prepared for inspections and audits right from the start.

Key Benefits of Working with Univita

  • Single-point responsibility: Streamlined execution without managing multiple contractors
  • Cost efficiency: Optimized engineering and procurement reduce both capital and operational expenses
  • Timely project delivery: Structured project management ensures adherence to deadlines
  • Future-ready design: Facilities planned for expansion and technological upgrades
  • Nationwide reach: Providing GMP support services across India, from major industrial hubs to emerging zones

Plant Modification Expertise – Upgrade, Retrofit & Expand with Complete GMP Compliance

Modernizing and upgrading existing pharmaceutical facilities is essential to ensure ongoing GMP compliance, improve operational performance, and align with changing regulatory and production requirements.
At Univita, we provide end-to-end pharmaceutical plant modification solutions designed around your business objectives, compliance needs, and future expansion strategies.
From small-scale retrofitting to full facility transformation projects, our experienced professionals ensure smooth, efficient, and compliant execution throughout every stage.
Recognized among leading pharma consultants in India, Univita delivers high-quality plant modification services across Europe, CIS, India, UK & Africa, supporting diverse pharmaceutical manufacturing setups.

Why Pharmaceutical Plant Modifications Matter

Pharmaceutical production facilities must continuously adapt to meet evolving global regulatory frameworks such as WHO-GMP, EU-GMP, US FDA, and MHRA. Plant modifications play a key role
  • Strengthening GMP compliance standards
  • Integrating advanced technologies and automation systems
  • Adjusting production lines for new requirements
  • Expanding manufacturing capacity
  • Improving utility systems and process workflows
  • Enhancing overall energy efficiency
  • Supporting introduction of new product segments
With us, clients benefit from well-planned retrofit and modification strategies that reduce downtime while maintaining uninterrupted operations.

Univita – Your Trusted Plant Modification Partner

Univita brings extensive experience in plant modification engineering and GMP-compliant facility upgrades. We deliver fully integrated turnkey solutions that are practical, compliant, and tailored to each client’s requirements—from initial planning through to final commissioning. Our capabilities include:
  • Cleanroom modification and layout optimization
  • Utility system rerouting and upgrades
  • HVAC redesign, balancing, and optimization
  • Facility expansion projects
  • Production line reconfiguration
  • Automation and control system integration
  • Equipment relocation and modernization
  • Electrical, fire safety, and civil infrastructure improvements

Our Core Service Areas

  • Customized plant modification solutions
  • Facility expansion and upgrade projects
  • Process plant improvement services
  • Existing facility renovation and adaptation
  • GMP-compliant facility enhancement solutions