Fabtech
Fabtech Technologies is a biopharma engineering company dedicated to building pharmaceutical and biotech capabilities worldwide. Their mission is to ensure access to affordable, life-saving medicines by providing innovative engineering solutions, turnkey projects, and advanced manufacturing equipment. They focus on quality, safety, and sustainability, supporting healthcare systems globally, especially in underserved regions. Their expertise includes cleanroom systems, water purification, containment solutions, and biosafety labs, all aligned with GMP standards. Fabtech aims to impact lives positively through their engineering excellence and collaborative approach, making them a reliable partner in the life sciences ecosystem. They are committed to upholding GMP standards, continuously striving for excellence and innovation in pharmaceutical engineering, and delivering start-to-finish engineering solutions for pharmaceutical and biotech companies worldwide.
Industries
Products
Modular cleanroom systems
Prefabricated, ISO-classified cleanroom units for rapid deployment and scalable expansion of controlled manufacturing or testing spaces.
Containment glove ports and half‑suit access systems
Standardized glove ports, glove-sleeve arrangements and half-suit assemblies providing airtight access and interchangeability for manipulation inside containment systems.
Aseptic filling lines (vial, ampoule, syringe, prefilled syringe)
Complete filling and closing machinery for aseptic liquid and powder filling with feeding, detection and rejection systems for quality control and isolator compatibility.
High-purity water generation systems
Systems producing purified water and WFI with continuous distribution and storage, designed to remove ions, particulates, organics and endotoxins for pharmaceutical use.
Pass-through chambers compatible with VHP decontamination
Static and dynamic pass boxes and pass-through chambers designed for integration with vaporized hydrogen peroxide decontamination workflows to maintain material transfer integrity.
Single-use bioreactor modules
Single-use bioreactor units and supporting disposable process equipment intended to reduce downtime and contamination risk in bioprocess workflows.
Modular cleanroom systems
Prefabricated, ISO-classified cleanroom units for rapid deployment and scalable expansion of controlled manufacturing or testing spaces.
Containment glove ports and half‑suit access systems
Standardized glove ports, glove-sleeve arrangements and half-suit assemblies providing airtight access and interchangeability for manipulation inside containment systems.
Aseptic filling lines (vial, ampoule, syringe, prefilled syringe)
Complete filling and closing machinery for aseptic liquid and powder filling with feeding, detection and rejection systems for quality control and isolator compatibility.
High-purity water generation systems
Systems producing purified water and WFI with continuous distribution and storage, designed to remove ions, particulates, organics and endotoxins for pharmaceutical use.
Pass-through chambers compatible with VHP decontamination
Static and dynamic pass boxes and pass-through chambers designed for integration with vaporized hydrogen peroxide decontamination workflows to maintain material transfer integrity.
Single-use bioreactor modules
Single-use bioreactor units and supporting disposable process equipment intended to reduce downtime and contamination risk in bioprocess workflows.
Services
Turnkey pharmaceutical engineering projects
End-to-end delivery including concept, design, procurement, manufacture, installation, commissioning and validation of pharmaceutical and biopharma facilities.
Cleanroom and containment systems supply and installation
Design, manufacture and install ISO-classified cleanrooms, containment enclosures, pass-throughs and associated air-handling systems for clinical and manufacturing environments.
Pharmaceutical process equipment manufacturing and integration
Custom manufacture of process lines and laboratory equipment and integration into contained production workflows for oral solids, sterile products and bioprocessing.
High-purity water systems supply, validation and consultancy
Supply and validation of PW/WFI systems and consultancy on water-treatment design, source-water adaptation, membrane selection and operator practices to ensure reliable regulatory-grade water production.
Validation, qualification and GMP readiness services
Execution of IQ/OQ/PQ, process and environmental validation, and preparation of regulatory-ready documentation and reports to support facility commissioning and inspections.
Cell and gene therapy cleanroom design and equipment supply
Design of ISO 5/BSL‑2 cleanrooms and supply/integration of equipment for gene and cell therapy workflows including biosafety cabinets, laminar flow hoods, incubators, cryostorage considerations and VHP-compatible pass-throughs.
Turnkey pharmaceutical engineering projects
End-to-end delivery including concept, design, procurement, manufacture, installation, commissioning and validation of pharmaceutical and biopharma facilities.
Cleanroom and containment systems supply and installation
Design, manufacture and install ISO-classified cleanrooms, containment enclosures, pass-throughs and associated air-handling systems for clinical and manufacturing environments.
Pharmaceutical process equipment manufacturing and integration
Custom manufacture of process lines and laboratory equipment and integration into contained production workflows for oral solids, sterile products and bioprocessing.
High-purity water systems supply, validation and consultancy
Supply and validation of PW/WFI systems and consultancy on water-treatment design, source-water adaptation, membrane selection and operator practices to ensure reliable regulatory-grade water production.
Validation, qualification and GMP readiness services
Execution of IQ/OQ/PQ, process and environmental validation, and preparation of regulatory-ready documentation and reports to support facility commissioning and inspections.
Cell and gene therapy cleanroom design and equipment supply
Design of ISO 5/BSL‑2 cleanrooms and supply/integration of equipment for gene and cell therapy workflows including biosafety cabinets, laminar flow hoods, incubators, cryostorage considerations and VHP-compatible pass-throughs.
Expertise Areas
- Turnkey pharmaceutical project management and execution
- Cleanroom and containment engineering for sterile manufacturing
- Aseptic fill–finish and sterile production line integration
- High-purity water system design, validation and operation
Key Technologies
- Modular cleanroom systems (prefabricated ISO-classified units)
- HEPA-filtered laminar airflow and laminar flow hoods
- Isolators and contained access interfaces (glove ports/glove sleeves)
- Aseptic filling and closing machinery (vial/syringe/ampoule)