The future of pharmaceuticals
Implementing automation into your pharmaceutical operations boosts efficiency, precision, and compliance, in turn enhancing product quality, and accelerating innovation for lasting industry success.Key services
Transform your pharmaceuticals lab processes with Labman’s advanced technological solutions.Transforming the innovation potential in drug development and production
Our extensive experience enables us to engineer cutting-edge solutions tailored to any drug discovery, clinical development, or manufacturing stage. We know automation is essential for streamlined workflows but also understand how crucial adhering to regulatory standards, ethical considerations, and cost-effectiveness is to ensuring responsible and sustainable drug development.Our Capabilties
Our mission is to enhance scientific pursuits with cutting-edge technology. Cultivating relationships with clients, some spanning over 25 years, emphasizes transparency and trust. Our dedicated team goes beyond transactions, actively engaging with clients for a profound understanding of project intricacies. This personalized approach distinguishes us and forms the foundation for consistently delivering technology that delights and inspires.- Hands-on team that will be your points-of-contact throughout the entire process of working with Labman.
- Mechanical, electrical, electronics and software are all in-house at Labman, so you can always be kept up-to-date with where every component is in the project.
- We keep an open door, so if you want to see your Labman technology at any stage in its development, you're always welcome to vist or to video call for updates.
- We understand the importance of industry compliance with all our custom projects meeting GxP regulation and FDA data integrity standards.
One modular system, endless possibilities
Our Bioprocess automation experts have extensive engineering and process experience with the development of manufacturing skids. These modular systems offer a huge range of scalability and flexibility to integrate seamlessly into your manufacturing operations. They comply with GMP 5 regulations with 21 CFR Part 11 to ensure data integrity. From chromatography , viral inactivation and filtration, these skids support the full scope of downstream purification.