Bulk Lot Release Testing

Every lot of biopharmaceutical production, requires a series of tests on both unprocessed and purified bulk material. All products entering domestic or global pharmaceutical markets require different tests to ensure safety and quality of the product.

TFBS offers a wide range of safety and quality testing services for various stage of biopharmaceutical products. All assays performed are fully validated in compliance with global regulatory requirements such as FDA, EMA and PMDA. Our experienced scientists can design a Lot Release Program base on the characteristics of your biopharmaceutical products, or adapt an existing program to meet your requirement.

TFBS provides a full range of support to our clients, from biosafety concerns to potency analysis to determining purity, identity and sterility of biopharmaceutical products. Our commitment is to provide one-stop contract services for all our clients and help minimize the time to product release.