1/8/2026China to Implement ICH E6(R3) Guideline for Drug Clinical Trial Qualit...

1/8/2026NMPA Clarifies Application of ICH Q12 to Strengthen Pharmaceutical Lif...

1/8/2026NMPA Moves to Accelerate Approval of Overseas-Approved Drugs for Urgen...

1/7/2026NMPA Issues Announcement on Strengthening Oversight of Contract Drug M...

1/6/2026China Solicits Comments on 102nd Batch of Reference Formulations for C...

1/4/2026China Sets New Records in Innovative Drug Approvals and Overseas Licen...

1/4/2026China Issues Fourth Batch of Encouraged Generic Drug List to Strengthe...

1/4/2026China Solicits Comments on Draft List of Newly Appointed External Drug...

1/1/2026CDE Issues the Technical Guidelines for Using Single-Arm Clinical Tria...

1/1/2026CDE Issues Technical Guidelines for Clinical Trials of Eosinophilic Es...

1/1/2026CDE Issues Technical Guidelines for Clinical Trials of Drugs Treating ...

1/1/2026CDE Releases Technical Guidelines for Targeted Biologics in Chronic Ai...

1/1/2026CDE Issues Technical Guidelines for Pan-Cancer Drug Clinical Developme...

1/1/2026NMPA Publishes 100th Batch of Reference Formulations for Generic Drugs

1/1/2026China's NMPA Issues Updated Bevacizumab Labeling Requirements

12/27/2025CDE Seeks Comments on Chinese Translation of ICH M8 eCTD Guidelines

12/27/2025NMPA Announces Adoption of ICH E6(R3) Guidelines for Clinical Trial Qu...

12/22/2025NMPA Announces Revision of Montelukast Product Labels to Strengthen Dr...

12/19/2025China Seeks Public Comments on Draft 101st Batch of Reference Formulat...

12/17/2025China Launches Pilot Program for Classified Management of Imported Foo...

12/17/2025CDE Solicits Comments on Draft Guidelines for Generic Ophthalmic Eye ...

12/17/2025China Opens Consultation on First ICH M13A Low-Risk Formulation List f...

12/15/2025CDE Solicits Comments on First Batch of ICH M13A Low-Risk Formulation ...

12/15/2025CDE Seeks Comments on Draft Technical Guidelines for Generic Ophthalmi...

12/5/2025China Issues Revised Guideline on Grading Adverse Events in Vaccine Cl...

12/5/2025China Releases 99th Batch of Reference Formulations Catalogue for Gene...

12/3/2025CDE Seeks Comments on Draft Guidelines Defining Major Deficiencies in ...

11/25/2025CDE Solicits Comments on Draft Guidance for Computerized Systems and E...

11/21/2025NMPA Issues New Rules on Inspections and Export Certificates for Drug ...

11/18/2025CDE Solicits Comments on Technical Guidelines for Common Clinical Issu...

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