Main products:Laboratory automation non-standard customization, pharmaceutical liquid preparation system, biopharmaceutical filling and packaging production line, pharmaceutical and reagent, freeze-dried microsphere packaging machine, laboratory bubble cap machine, bubble cap packaging machine, liquid capsule preparation machine, etc
Recommended product: Automated sterile pharmaceutical filling machine
The automated sterile pharmaceutical filling machine is a compact solution for automatic filling lines. Suitable for small, medium, and small-scale production filling lines in pharmaceutical companies, biotechnology companies, in vitro diagnostic companies, and cosmetics companies.
Automated aseptic pharmaceutical filling machine
Product Features:
(1) A modular, efficient, and flexible system. Can complete various small-scale, multi batch, and multi variety automated sterile pharmaceutical filling machine projects
(2) Compatible with multiple bottle types, enabling flexible transformation of various bottle types, sizes, and cap types and sizes
(3) High cleanliness, matched laminar flow hood, isolator, etc., can achieve online monitoring of particles and floating bacteria
(4) Can match disposable sterile filling process, eliminate cross contamination, simplify cleaning certification
(5) High precision filling: filling volume range from 1ul to 100ul, with a repeatability accuracy of ± 1%
(6) Mechanical structure linkage control is adopted for execution and linkage to improve accuracy, precision, and system stability
(7) Strong scalability, expandable high-speed bottle sorting machine, capping machine, automatic homogenization, emulsification, automatic liquid preparation, etc
(8) High efficiency: Design unit filling/dual position filling/multi position filling methods
(9) The equipment is controlled by PLC or industrial computer, based on industrial Ethernet communication, and can interact with enterprise ERP system or LIMS management software to achieve digital factory
(10) High level of intelligence, software meets the requirements of FDA 21 CFR PART 11 for electronic records. Multi sensor feedback is used on site to monitor the production site in real-time. The software system integrates functions such as personnel management, electronic review, electronic signature, batch management, production statistics, audit tracking, and can generate data records, trends, reports, and graphics.
The company currently integrates design automation, non-standard design, manufacturing, intelligent design, software development, and integrated services. It has self operated import and export rights and maintains good cooperative relationships with numerous universities, research institutes, pharmaceutical manufacturers, testing institutions, etc. at home and abroad.