Creative Biolabs is offering the most comprehensive services for antibody development projects. With strict regulation and effective execution, we are dedicated to providing the most valuable solutions to complete your projects.
HighlightsCreative Biolabs is offering the most comprehensive services for antibody development projects. With strict regulation and effective execution, we are dedicated to providing the most valuable solutions to complete your projects.
HighlightsCreative Biolabs has established a broad range of platforms for developing novel antibodies or equivalents. These cutting-edge technologies enable our scientists to meet your demands from different aspects and tailor the most appropriate solution that contributes to the success of your projects.
HighlightsWith deep understanding in antibody-related realms and extensive project experience, Creative Biolabs offers a variety of references to help you learn more about our capacities and achievements, including infographic, flyer, case study, peer-reviewed publications, and all kinds of knowledge that can assist your projects. You are also welcome to contact us directly for more specific solutions.
HighlightsGet a real taste of Creative Biolabs, one of the most professional custom service providers in the world. We are committed to providing highly customized comprehensive solutions with the best quality to advance your projects.
HighlightsCreative Biolabs can supply you the services on bio-manufacturing with traditional or novel bioreactors, both of them are certificated and licensed. A novel but certified bioreactor improves the traditional ones through oxygen transfer method. The new designed bioreactor can eliminate the blades which are caused by rotating blades and air sparging, and it can attract oxygen from ambient air efficiently. After process development, large scale fermentation or called cGMP manufacturing will be involved.
Large-Scale Fermentation
Distributed under Unsplash License, from Unsplash.
Creative Biolabs' staff scientists will transmit the process which is validated from the first Feasibility Study step to cGMP manufacturing staff and QC in a collaborative manner. The process development is the key for filing FDA IND CMC part. The manufacturing process will not be changed when clinical trials initiate.
Our validated equipment is designed by highly reputable suppliers, and the suites with full flexibility and quality are engineered by our team to achieve our shared objectives, and that ensures us a consistent and in-controlled operation.
All listed services and products are For Research Use Only. Do Not use in any diagnostic or therapeutic applications.
