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R&D Ability

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Technology & equipment

According to the domestic and international drug registration requirement, the Peptide R&D center build the Standardized system including quality assurance QA system, R&D process risky management system and quality technology transfer system to guarantee the peptide R&D process always comply with the FDA and the CFDA registration requirements.

 

 

Peptide drug R&D center is equipped with the domestic first-class pharmaceutical R & D polypeptide hardware and software, with all kinds of advanced equipment, such as the United States SSI Prep-2000 high performance preparative liquidLC, Agilent LC-MS system Q-TOF6530, DAC-100 DAC-150 and trans phase preparation system, the US GE’S AKTA pure M1 chromatography development process chromatography systems, and other advanced equipment.

 


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