Industry 10 / 10
R&D Facilities
Research and development facilities must stay flexible as programs change, while pilot and clinical-supply areas still need GMP-grade control. Modular room planning, spare service capacity, and a clear boundary between development and GMP zones keep future reconfiguration practical.
Engineering focus
- 01
Modular laboratory and pilot suite planning for changing programs
- 02
Clear boundaries between development and GMP clinical-supply zones
- 03
Flexible utility drops and spare service capacity
- 04
Scale-up and technology transfer to commercial production
Relevant services
- 02Master Planning & Concept EngineeringZoning, flows and phasing fixed early, while changes are still inexpensive.
- 03Facility & Architectural DesignPharmaceutical architecture shaped by the process, the people and the flows between them.
- 06Process UtilitiesSteam, air, gases, water and drainage systems sized and specified for regulated production.
- 07GMP & ComplianceFacility design reviewed against GMP requirements at every stage.
- 09Project ManagementOne point of control for scope, cost, schedule and interfaces.
Next step
Planning a pharmaceutical project?
Share the product type, the current stage and the main constraints. We will respond with a proposed scope and next steps.
+20 101 171 1700