PHARMACEUTICAL & LIFE SCIENCES EPC
From Project Concept to a GMP-Ready Facility
GENO aligns process planning, multidisciplinary engineering, cleanroom systems, procurement, construction, commissioning and qualification support within one accountable project framework—helping owners control critical interfaces across design, supply, site execution and start-up.
For greenfield, expansion and facility-upgrade projects.
Structure · Production · Technical Mezzanine / Concept
Process-led Planning
Integrated Engineering
Controlled Supply Chain
Commissioning & Qualification Support
PROJECT ACCOUNTABILITY
One Project. One Accountable Delivery Team.
The highest project risks often sit between process, layout, HVAC, utilities, equipment, construction and qualification. GENO brings these interfaces into one controlled delivery framework.
Coordinate before construction
Control interfaces during delivery
Prepare evidence for handover
PROJECT LIFECYCLE
Full-Lifecycle EPC Delivery
Seven connected stages move the project from controlled requirements to start-up and handover.
CONCEPT
Establish the project, process and flow basis before design expands.
- Project basis
- Process concept
- Scope matrix
DESIGN
Coordinate disciplines, equipment and utilities against one design basis.
- Coordinated layouts
- System specifications
- Interface register
DELIVERY
Control procurement, manufacturing, construction and installation against approved information.
- Procurement packages
- Inspection records
- Site documentation
START-UP
Prove system readiness and organize qualification and handover evidence.
- Commissioning records
- CQV support
- Turnover dossier
ENGINEERING IN PRACTICE
From Coordinated Design to Site Execution and Handover.
Concept illustrations of design, installation and handover. AI-generated, not photographs of completed projects.
Recent Projects
Contractual scope and current stages of GENO projects. Design renderings do not represent completed or certified facilities.
Material procurement
BIOPharma Korea
BIOPharma Korea cleanroom project in Jecheon, Republic of Korea. Contract scope: design, cleanroom envelope, HVAC and MEP, procurement, installation, commissioning, DQ/IQ/OQ and BIM rendering. Design basis: GMP. Signed 26 August 2026; planned duration: 120 days from the seller’s receipt of the advance payment.
Send Your Inquiry
Contract signed · Awaiting commencement
Prex Pharma
Prex Pharma facility in Jeddah, Saudi Arabia. Contract scope: civil EPC, cleanrooms and process equipment supply. Awaiting the first advance payment and commencement conditions; construction has not started. Planned duration: 730 days from the seller’s receipt of the advance payment.
Send Your InquiryFACILITY SOLUTIONS
Facilities We Support
Facility concepts are shaped by product, process, risk and target-market requirements.
Pharmaceutical Manufacturing
Process-led facilities for oral solid dose, liquid, topical and related operations, coordinated around containment, equipment, utilities and target-market requirements.
Learn MoreAseptic & Biotechnology Facilities
Aseptic and biotechnology environments coordinated from the outset around contamination control, segregation, critical utilities, environmental stability and the project qualification strategy.
Learn MoreMedical Device Facilities
Controlled assembly and packaging environments shaped by product cleanliness, particle sensitivity, material flow, inspection needs and the justified quality basis.
Learn MoreLaboratories & R&D Environments
Flexible laboratory and development environments integrating workflows, equipment, samples, ventilation, utilities, personnel safety and future operational change requirements.
Learn MoreHealthcare & Special Medical Environments
Selected healthcare and special medical environments coordinated around air quality, pressure relationships, hygiene, specialist equipment and operational continuity requirements.
Learn MoreAdvanced Clean Manufacturing
Clean production environments engineered around particle, temperature, humidity, electrostatic, chemical, vibration and utility-stability risks for sensitive manufacturing operations.
Learn MoreFACILITY SYSTEMS
Integrated Cleanroom & Facility Systems
Room, air, utility, equipment and control systems are coordinated as one facility relationship.
CONTROLLED FACILITY INTERFACEGENO coordination
01PROCESS
02CLEANROOM
03HVAC
04UTILITIES
05EQUIPMENT
06MEP
07CONTROLS
DELIVERY ECOSYSTEM
An Integrated Delivery Ecosystem
GENO remains the project-facing technical, commercial and coordination interface while project-specific engineering, supply and local execution resources work within a controlled responsibility structure.
PROJECT OWNER
GENO PHARMATECHEPC PROJECT COORDINATION
EngineeringProcurementManufacturing NetworkConstructionCommissioning & CQVLocal Execution Support
PROJECT REQUIREMENTS
Designed Around Target-Market Requirements
Applicable classifications, technical standards, deliverables and qualification responsibilities are defined through each project's URS and contract.
ISO 14644EU GMP / Annex 1WHO GMPApplicable FDA cGMP Requirements
References do not imply certification or regulatory approval. The applicable framework is confirmed through the project URS and contract.
PROJECT QUESTIONS
Clear Answers Before the First Discussion
Four practical questions for owners preparing an EPC project review.
01Can GENO deliver a complete turnkey pharmaceutical facility?
GENO can structure a coordinated EPC or turnkey delivery scope across planning, engineering, controlled procurement, construction, commissioning and qualification support. The exact scope, local statutory roles and owner responsibilities are defined through the URS and contract.
02Can GENO work with local civil and installation contractors?
Yes. GENO can coordinate with qualified local contractors where the execution model requires local civil works, labor, permits or installation resources. Interfaces, supervision, quality controls and responsibility boundaries must be agreed before site work begins.
03Can GENO support commissioning and DQ/IQ/OQ/PQ activities?
GENO can support agreed commissioning, testing, documentation and qualification activities, including interfaces with DQ, IQ, OQ and PQ plans. Validation strategy, product qualification and regulatory acceptance responsibilities remain project-specific.
04What information should I send for the first project review?
Share the product and dosage form, planned capacity, target market, site or building data, process flow, equipment list, current layout, utility information and target schedule. Preliminary inputs are acceptable when assumptions and gaps are clearly identified.
01PROJECT DEFINITION
PROJECT INSIGHT
What Information Is Needed to Start a Pharmaceutical Facility Project?
A practical checklist covering product type, capacity, target market, site conditions, process flow, cleanroom classification, utilities, schedule and project delivery model.
Read the project readiness checklistNEXT PROJECT STEP
Planning a Pharmaceutical Facility?
Share your product, capacity, target market, site information and current layout. These inputs will help structure the first technical discussion and identify the next engineering steps.