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On June 7, 2022, CDE released the Annual Report on the Progress of Clinical Trials for New Drug Registration in China (2021). Based on the registration information of the drug clinical trial registration and information disclosure platform, the report comprehensively summarizes and analyzes the status quo of new drug registration clinical trials in China in 2021, and compares and analyzes the changing trend characteristics in the past three years.
2023-02-02
On July 18, 2022, the groundbreaking ceremony of the first phase of CDMO laboratory construction and the unveiling ceremony of the three major bases of Changrui Biotechnology (Chengdu) Co., Ltd. (hereinafter referred to as "Changrui Biotechnology") were held in Chengdu Tianfu International Biocity.
Changrui Biotechnology (Chengdu) Co., Ltd. entrusted Chengdu Green Island Enterprise Management Co., Ltd. to undertake the preparation of the environmental impact report of the carrier drug development and macromolecule biodrug R&D and pilot scale-up service platform project, and according to the Measures for Public Participation in Environmental Impact Assessment (Order No. 4 of the Ministry of Ecology and Environment), the relevant information of the project is hereby published as follows:
October 24, 2022 is a memorable day in the development history of Changrui Biotechnology, and all employees congratulated the housewarming at the new site of the company, Chengdu Tianfu International Biocity Area C Office Building.
Macromolecular Biopharmaceutical Research*
Changrui Biologics - a public technical service platform for vector drug development and macromolecular biopharmaceutical research
Changrui Biotech participated in the 2022 college campus job fair
Changrui Biotech participated in the signing ceremony of Chengdu Tianfu International Biocity with a total investment of more than 11 billion yuan - 2022 circle building strong chain project
2021 Annual Drug Evaluation Report Released - These issues are worth paying attention to
CDE issued three guiding principles, including the Technical Guidelines for Pharmaceutical Research and Evaluation of In Vivo Gene Therapy Products (Trial).