Charles River has more than 20 years of experience in developing customized manufacturing services to meet clients' unique needs. Our current Good Manufacturing Practice (cGMP)-compliant biopharmaceutical manufacturing capabilities complement our testing services to help accelerate the development of a biologic from concept to product release.
Biologics Manufacturing & Production Services
From early preclinical formulation development through clinical and commercial manufacturing and release, we provide timely, tailored science and services to support cGMP large molecule manufacturing. Our team of scientists can ensure the quality, consistency and integrity of a client's cell and viral banks, promoting a smooth and successful outcome for their manufacturing campaigns.
Our manufacturing/production capabilities include:
|기본 배송비||교환/반품 배송비|
결제 및 환불 안내
교환 및 반품 접수
|교환 및 반품 접수 기한|
|교환 및 반품 접수가 가능한 경우|
|교환 및 반품 접수가 불가능한 경우|
교환 및 반품 신청
Charles River의 다른 상품들
Charles River has more than 20 years of experience in developing customized manufacturing services to meet clients' unique needs.
Extensive cell line characterization is required for mammalian, microbial and insect cell substrates used to generate biopharmaceuticals. This includes phenotypic or genotypic identity testing and a broad range of adventitious agents testing.
To help clients generate the data needed to gain the level of product characterization required for regulatory submission, Charles River offers protein analysis as part of an integrated package of expert analytical services.
Clearance studies are an essential part of a manufacturer’s program to ensure product safety.
To ensure that client biopharmaceuticals, pharmaceuticals and medical devices are produced according to the strict requirements of Good Manufacturing Practice (GMP)