GENO Pharmatech implements the strategy of 'strong alliance and establishes in-depth cooperative relationships withmany senior design instiutes in the industry to complement each other's advantages Adhering to the "customer-cen-ered" service concept, the Company provides customers with professional technical services throughout the full lifecycleservices from concept to qualified facility, including project feasibility study, investment decision-making and projectimplementation management, with 17 years of experience and professional accumulation in the industry.
Business Direction
We provide integrated professional services throughout the entire lifecycle of pharmaceutical projects, from strategic planning in the early stages to operational support in the later stages, to create comprehensive solutions for pharmaceutical companies and related parks.
In the project consulting phase, we focus on the core needs of the industry, conduct market and regulatory policy research, and help enterprises accurately grasp industry trends and compliance requirements; Thoroughly analyze the investment feasibility of pharmaceutical parks and factories, combined with business models and financial analysis, to provide scientific basis for project investment decisions; At the same time, we provide GMP/FDA/EU regulatory compliance consulting, tailor project roadmaps and execution strategic plans to ensure that projects are aligned with industry standards and corporate development goals from the outset.
In the engineering design phase, we have professional capabilities in pharmaceutical facility design, covering overall planning of pharmaceutical facilities, GMP lounge and containment design, as well as core content such as process design (PFD, P&ID), utility system design (HVAC, PW), etc. We also use Building Information Modeling (BIM) technology to visualize and refine the design process, laying a solid foundation for subsequent construction and operation.
Procurement and configuration services are committed to building an efficient supply chain system, integrating high-quality resources through global procurement of process equipment; Provide pharmaceutical production line integration, process equipment configuration, and automation and control system integration services to ensure smooth connection of production processes; At the same time, relying on professional logistics and supply chain management capabilities, ensure timely and accurate delivery of equipment and materials.
In terms of engineering management, we focus on turnkey EPC project management, coordinating key aspects such as GMP cleanroom construction, public works, and process pipeline installation; Strictly control progress, quality, and cost, and establish a full process control system; Always adhere to safety and HSE compliance standards to ensure the safe and standardized construction process of the project.
In the professional service phase, we provide comprehensive support for project implementation and compliance operation, including technical services such as system debugging (CX), equipment identification (IQ/OQ/PQ), GMP validation support (process/cleaning), etc; Provide facility start-up assistance to assist in the rapid production of projects; Conduct operator and maintenance training to enhance the professional skills of enterprise personnel.
Operation and maintenance services focus on the long-term stable operation of projects, providing facility management services, establishing preventive maintenance procedures, and reducing equipment failure risks; Improve production efficiency and resource utilization through process optimization and energy-saving solutions; Continuously providing regulatory qualification re certification support to ensure the continuous compliant operation of enterprises; Simultaneously provide spare parts and technical support to promptly solve various problems during operation.
GENO Pharmaceutical Technology provides a one-stop integrated solution covering laboratory "design consulting + engineering installation + after-sales operation and maintenance" for biological laboratories, physical and chemical laboratories, animal room laboratories, P3 laboratories, etc. of medical institutions, disease control centers, universities, inspection and testing institutions. This includes overall planning and design consulting, implementation of decoration, HVAC, ventilation, electrical, water supply and drainage, special gas system engineering, construction of intelligent management platforms and safety management platforms for laboratories, production and installation of laboratory supporting furniture and equipment, and other services.
Our services cover the full lifecycle management of pharmaceutical equipment, from planning, procurement, installation and commissioning to daily operation and maintenance, fault repair, preventive maintenance, and technical upgrades. We also provide value-added services such as compliance verification, personnel training, and digital system construction to help pharmaceutical companies achieve efficient, stable, and compliant equipment operation.
The EPC service for cleanroom projects covers the entire process: from preliminary requirement research, standard establishment and scheme design, to the procurement of core purification equipment and building decoration materials, to the construction of the main structure, purification system and auxiliary system, and finally to the completion of commissioning and testing, completion acceptance and personnel training, as well as providing one-stop services such as maintenance and upgrading in the later stage, to ensure the efficient and standard operation of the cleanroom.
Antibody production can be divided into three major stages: upstream (cell culture to harvest), downstream (purification to filling), and formulation. According to the process, a complete upstream and downstream process system can be provided for the preparation of denosumab, tocilizumab, rituximab, trastuzumab, etc.