As a professional full-lifecycle Cleanroom Engineering Contractor, GENO is committed to providing turnkey cleanroom solutions—from conceptual design and project implementation to overall delivery—for high-tech industries such as pharmaceuticals, biotechnology R&D, food manufacturing, and semiconductors.

We hold multiple core qualifications, including architectural design, general contracting for construction, general contracting for mechanical and electrical construction, and specialized contracting for building mechanical and electrical installation projects.

We strictly adhere to international GMP standards, including China GMP (2010 Revision), EU GMP Annex 1, and FDA cGMP, to provide compliant and reliable cleanrooms for the pharmaceutical and food manufacturing. Basing the ISO 14644 series of standards as our design benchmark, our services cover the construction of semiconductor cleanrooms ranging from ISO Class 1 to ISO Class 8.

Supported by 18 years of industry accumulation, national high-tech enterprise qualifications, multiple national construction awards and a global service network covering North America, Europe and Southeast Asia, our integrated EPC model eliminates multi-party coordination risks and unifies all design, production and construction standards for every high class cleanroom project.

1 Vertically Integrated Hardware Support

We maintain self-production lines to support matched EPC system delivery, with our in-house product lineup split into three core categories:

1. Cleanroom Envelope System: Clean wall panels & airtight clean doors

2. Purification Terminal Equipment: FFUs & air supply diffuser systems

3. Independent Cleanroom HVAC System for full environmental regulation

All hardware adopts unified design standards to avoid cross-component compatibility issues during on-site construction.

2 Full-Lifecycle Pharmaceutical Cleanroom EPC Unified Execution Framework

As a professional Cleanroom Engineering Contractor, our core value lies in single-source accountability covering the entire project lifecycle, a distinction separate from hardware merchants without construction general contracting capacity. Our standardized EPC workflow follows a sequential, interlinked engineering logic:

1. Front-End Regulatory & Process Consulting: URS sorting, site survey, process flow planning and regulatory alignment layout design, referencing global industry standards as applicable to the target market

2. Integrated System Engineering: Unified coordination of enclosure, HVAC, utility, process pipeline and intelligent monitoring via BIM clash detection

3. Centralized In-House Manufacturing: Batch production of all structural and air treatment hardware under unified design specifications

4. Site Turnkey Construction: Centralized management of panel assembly, HVAC piping, electrical and special gas installation under one project team

5. Commissioning & Validation Support: Air balance testing, particle verification and complete IQ/OQ/PQ documentation assistance for audit preparation

6. Long-Term Global Technical Support: Spare parts supply, maintenance training and system upgrade consulting for all delivered Cleanroom Facility

Clients only liaise with one GENO project team throughout the whole cycle, removing fragmented responsibility and cutting cross-party communication overheads significantly. Supported by our long-term strategic alliances with top domestic design institutes, we can also expand service scope to pharmaceutical park infrastructure, laboratory complexes and hospital operating room integrated projects based on client demands.

3 Core Differentiators of GENO’s Integrated EPC Turnkey Model

Most competitors separate product supply and construction execution into independent business segments, leading to inconsistent technical benchmarks. Our vertically integrated EPC system delivers tangible project advantages for facility owners:
✅ Single contractual accountability covering all structural, HVAC, utility and auxiliary engineering scope
✅ Unified cross-system design standards from the drawing stage, eliminating component interface conflicts
✅ Optimized overall layout engineering to lower long-term energy consumption and routine maintenance costs
✅ Modular design framework adaptable to pharmaceuticals, biotech, medical laboratories, hospitals and food controlled environments
✅ Material formulations engineered to accommodate regular VHP disinfection cycles in sterile classified areas
✅ Fire-retardant, low-shed structural materials aligned with mainstream facility operation requirements
✅ Global service network covering 30+ countries, with local after-sales teams and completed local reference projects
✅ Full industrial chain extension capability: supporting API supply, pharmaceutical technology transfer, digital data platform and financial matching services for full-factory ecosystem construction

4 Brand Commitment: Customised Turnkey Solutions Aligned With Global Regulatory Requirements

Guided by our mission Pure Heart, Promise Kept, GENO focuses on scalable, operationally efficient Turnkey complete cleanrooms. Our product and engineering frameworks can be tailored for projects referencing ISO 14644, EU GMP Annex 1 and FDA regulatory requirements, without universal compliance overstatements.

Whether your project involves new greenfield pharmaceutical plants, biotech laboratory retrofits or hospital sterile facility upgrades, our integrated Cleanroom Turnkey Solution and full-spectrum EPC services can be adjusted to match your unique process, budget and validation targets.

If you are seeking a unified EPC general contractor with integrated hardware manufacturing, cross-system design coordination and global project delivery experience, connect our senior engineering team for customised project quotations, full catalogues and verified cross-border facility references.
Official Website: https://www.genopharmatech.com