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Design & Build Services | Turnkey GMP Pharma Facility Execution Dubai - Pharma Connect
Design & Build

From design intent to facility readiness.

Design and Build brings facility planning and execution into one integrated pathway. We align engineering, procurement, construction, cleanroom installation, MEP systems, automation, CQV and handover under one coordinated delivery. One accountable team, one connected pathway.

Delivery ModelSingle accountability
CoverageProcure, Build, CQV
OutcomeValidated & operational
Pharmaceutical facility under turnkey construction
From engineering to handover
The approach

Integrated delivery. One accountable team.

We support pharmaceutical companies from design intent through to a validated, operational facility. Engineering, procurement, construction, cleanroom installation, MEP, automation, CQV and handover are coordinated as one connected delivery pathway, helping maintain alignment across every stage of the project.

Each part of the scope below is a discipline in its own right. Explore any of them to see how we plan, build and validate it.

The delivery pathway

Four phases, one connected delivery pathway.

One coordinated path from design to operation.

Each phase flows into the next, keeping engineering intent, procurement, installation and CQV aligned throughout the project. One coordinated delivery approach helps maintain continuity from early design through execution, qualification and final handover.

Procurement
Construction
CQV
Phase 01

Engineering

Process requirements, facility layouts, cleanrooms, HVAC, utilities, MEP, automation and equipment interfaces are developed into coordinated engineering information for procurement and execution.

Phase 02

Procurement & Supplies

Procurement planning, vendor coordination, technical bid evaluation, equipment and material sourcing, delivery tracking and supply alignment with approved engineering specifications.

Phase 03

Construction & Installation

Site mobilisation, coordinated execution and installation across cleanroom systems, MEP services, utilities, automation and equipment interfaces.

Phase 04

CQV & Compliance

Process requirements, facility layouts, cleanrooms, HVAC, utilities, MEP, automation and equipment interfaces are developed into coordinated engineering information for procurement and execution.

Design & Build Scope

Integrated disciplines, one connected delivery approach.

Explore the full Design & Build scope across the disciplines involved in pharmaceutical facility delivery. Each service is coordinated as part of one connected pathway, from engineering through execution and handover.

01

Process Design & Facility Flow

Utility integration, capacity and line balancing, operability and HAZOP, shaped around how the plant actually manufactures.

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02

Cleanroom & GMP Layouts

Cleanroom classification, pressure cascades, personnel and material flow, airlocks and cleanroom systems coordinated around contamination control and GMP operations.

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03

HVAC & Environmental Control

HVAC supports the environmental conditions required to maintain the classified environment. WHO guidance treats contamination and cross-contamination control as fundamental HVAC design considerations.

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04

Mechanical, Utilities & Piping

Piping distribution, pumps, manifolds, drainage and equipment interfaces designed to applicable engineering and project standards.

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05

Electrical & Lighting

Transformer and DG sizing, panels, UPS, load studies, lighting and earthing designed for safe, reliable power distribution and continuity of critical loads.

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06

Clean & Black Utilities

Purified water, WFI, pure steam, process air and supporting black utilities engineered for reliability and compliance.

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07

Automation, ELV, BMS & EMS

Process automation, building management, environmental monitoring, ICT, access control and security coordinated across connected facility platforms.

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08

QC Laboratory & Specialty Areas

Lab layouts, furniture and sample flow, plus warehousing, logistics, waste management and specialty support spaces.

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09

Construction & Installation

Site mobilisation, coordinated installation, inspection, documentation, system testing and handover aligned with approved engineering and site requirements.

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10

CQV & Compliance Readiness

Commissioning, qualification and validation planned through risk-based strategies aligned with applicable GMP requirements and recognised guidance.

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One accountable team, one connected pathway

Ready to build?
Let's engineer the path to it.

Whether you are scoping a new facility or expanding an existing one, we will take it from approved design to a validated, operational facility.