Merck expands biodevelopment centers in North America, China and Europe

Merck, a leading science and technology company, has announced the expansion of its end-to-end biodevelopment centers to meet increasing customer demand for its turnkey portfolio of bioprocessing products, manufacturing capabilities and industry leading technological expertise.
The expansion, which includes the opening of two new process development centers in the US and China, follows the commercial success of Merck’s biodevelopment center in Martillac, France. The two new units will be located in close proximity to customers in the Shanghai and Boston metropolitan areas. Each will provide a full range of process development capabilities and services. This includes cell line development services, both upstream and downstream process development, as well as non-GMP clinical production.
“We are seeing an increasing global demand for end-to-end process development solutions and Merck offers a one-stop shop for biopharma customers,” said Udit Batra, Member of the Merck Executive Board and CEO, Life Science. “This expansion reinforces our position as the premier supplier of all process development and clinical stage manufacturing solutions, materials and services needed for the production of biologics. This is a strategic, high-potential investment for Merck specifically designed to meet customer needs on three continents.”
Merck’s biodevelopment center in Martillac, France, is a fully operational single-use, GMP facility for manufacturing clinical stage batches. Equipped with a full suite of Merck technologies, including the 2000 liter single-use Mobius® bioreactor, Martillac offers biopharma companies a complete solution to support their clinical development programs.
Merck’s end-to-end offering delivers important benefits and addresses key challenges for biopharmaceutical companies at all stages of molecule development and commercialization in any geography. In addition to the Mobius® bioreactor, the end-to-end portfolio includes solutions such as Lynx® CDR, Viresolve® Process Area Modules, Pellicon® and Centinel™ Intelligence Virus Defense.
Early-stage companies with limited resources and infrastructure benefit from a partner with strong expertise and experience developing processes and GMP clinical manufacturing to help accelerate early clinical development programs. Companies in more advanced stages need to overcome the challenges of moving from late phase clinical development into commercial manufacturing, accelerating availability of affordable life-enhancing drugs. With an end-to-end approach, Merck can facilitate and accelerate scaling and technical transfer of an entire process to a new location.