NEB Enhances Rowley Facility for Demanding Product Specs
New England Biolabs (NEB) has announced enhanced manufacturing capabilities at its Rowley facility. The site now operates under more stringent infrastructure and process controls to meet increasingly demanding product specifications and customer requirements.
NEB's commitment to quality is evident in its Rowley facility, which is certified to both ISO 9001 and 13485 standards. The company's dedication to Good Manufacturing Practice (GMP) grade production ensures high-quality products for its clients.
NEB offers comprehensive support to its clients through dedicated account managers, technical scientists, and production and quality teams. This personalized collaboration allows NEB to work as an extension of its clients' teams, providing tailored solutions.
The company's Customized Solutions Team, based in Frankfurt am Main, specializes in helping clients navigate the complexities of regulated markets. They assist in accessing novel products, meeting quality specifications, speeding up time to market, and streamlining supply chains. Despite the lack of information on the leadership of this team, their expertise is undeniable, with the company boasting 50 years of experience in enzymology and reagent manufacturing.
NEB's enhanced manufacturing capabilities at its Rowley facility, coupled with its comprehensive support services and customized solutions, position the company to meet the evolving needs of its clients. While NEB does not manufacture Active Pharmaceutical Ingredients (APIs) or operate in full compliance with all Current Good Manufacturing Practice regulations, its commitment to quality and personalized collaboration ensures high-quality products and services.
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