For near-approved ADC new drugs, attention needs to be turned to the current good manufacturing practice (cGMP) in preparation for scale-up and commercialization. ADCs need to be prepared according to the general regulations and guidelines required by sterile drug manufacturers. The ADC manufacturing team of BOC Sciences provides ADC fill/finish process services with our state-of-the-art development and manufacturing facilities. Our fill/finish equipment can automatically fill, plug and edge multi-specification containers and closed configurations.
We offer high performance aseptic filling and finishing capabilities, including complete integrated fill and finish lines. The filling and finishing of our ADC is carried out in strict accordance with the FDA's cGMP guidelines, and an independent quality department has been set up to conduct a comprehensive review of the production process.
With manufacturing facilities in the US and UK, we provide non-cGMP/cGMP pilot and commercial scale solutions for your ADC. Our ADC manufacturing capabilities include:
BOC Sciences has provided world-class ADC development and manufacturing services at competitive prices for many years. In addition to providing various preclinical R&D technical support, we also provide ADC scale-up and commercialization contract manufacturing services. Our products follow the analysis of quality assurance (QA) procedures to ensure delivery of high-quality finished products that meet customer requirements. If you have any needs about ADC filling and finishing, please feel free to contact us for more information.
BOC Sciences' cGMP manufacturing can prepare ADCs for scale-up and commercialization. We have strict cGMP manufacturing standards, including scientific isolation controls, rigorous cleaning and sterilization processes, and FDA-compliant production and purification facilities.