7/25/2024CDE Solicits Public Comments on the Technical Guidelines for Quality C...

7/24/2024CDE Solicits Public Comments on the Guidelines for Setting Limits on R...

7/24/2024CDE Solicits Public Comments on the Technical Guideline for the Study ...

7/19/2024CDE Solicits Public Comments on the Technical Guidelines for In Vitro ...

7/18/2024NMPA Suspends Import, Sales and Use of Daiwoong's Cefodizime Sodium fo...

7/18/2024NMPA Solicits Public Comments on Drafts of the 'GMP for Pharmaceutical...

7/17/2024CDE Issues the Technical Guidelines for Clinical Trials of Drugs for G...

7/17/2024CDE Solicits Comments on Draft Implementation Suggestions and Chinese ...

7/17/2024CDE Solicits Comments on the Technical Guidelines for Non-Clinical Res...

7/16/2024NMPA Announces Package Insert Revision of Spleen Polypeptide Injection...

7/15/2024CDE Solicits Comments on the Technical Guidelines for IVRT and IVPT St...

7/12/2024CDE Solicits Public Comments on ICH M14 and Its Chinese Translation

7/10/2024MOST Committee Issues the Ethical Guidelines for Human Genome Editing ...

7/9/2024CDE Solicits Comments on the Technical Guidelines for Drug Exposure-Ef...

7/9/2024CDE Solicits Comments on the Technical Guidelines for Clinical Pharmac...

7/8/2024CDE Issues the Technical Guidelines for Pharmaceutical Research on Ora...

7/8/2024NMPA Vice Commissioner Meets Senior Dutch Healthcare Officials.

7/5/2024CDE Solicits Comments on the Technical Guidelines for Non-Clinical Res...

7/5/2024CDE Issues the Technical Guidelines for the Study of Overfilling in Ge...

7/3/2024NMPA Announces Package Insert Revision of Dihydroxypropyl Theophylline...

7/1/2024CDE Issues the Notice on Pilot Implementation of Electronic Drug Regis...

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