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1-805-304-6109 info@hillgene.com
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Hillgene News & Blog
CDE issued “Guidelines on Clinical Trial Statistics of Drug Products for Rare Diseases (Interim)”
Jun 07 2022
CDE issued “Guidelines on Clinical Trial Statistics of Drug Products for Rare Diseases (Interim)”
Jun 07 2022
The Comprehensive Affairs Department of NMPA Solicits Public Comments on “Inspection Procedures of Drug Product MAHs (Draft for Comments)”
Mar 02 2020
The Comprehensive Affairs Department of NMPA Solicits Public Comments on “Inspection Procedures of Drug Product MAHs (Draft for Comments)”
Mar 02 2020
Center for Drug Evaluation (CDE) Issued the Notification of “Technical Guideline for the Pharmaceutical Study and Evaluation of Ex-vivo Genetic Modification System (Interim)” (No. 29, 2022)
Jun 01 2022
Center for Drug Evaluation (CDE) Issued the Notification of “Technical Guideline for the Pharmaceutical Study and Evaluation of Ex-vivo Genetic Modification System (Interim)” (No. 29, 2022)
Jun 01 2022