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  • 7/31/2023CDE Announces Office Relocation and Related Matters
  • 7/28/2023CDE Solicits Comments on Technical Guidance for Clinical Pharmacologic...
  • 7/27/2023CDE Solicits Comments on Bioequivalence Study Guidelines of Five Gener...
  • 7/27/2023CDE Issues on Three Guideline Documents on Patient-centered Clinical R...
  • 7/27/2023CDE Issues on the Guidelines for the Study of Disease Natural History ...
  • 7/25/2023CDE Solicits Comments on the Technical Guidelines for Clinical Applica...
  • 7/25/2023CDE Solicits Comments on the Technical Guidelines for Clinically Relev...
  • 7/25/2023CDE Issues the Technical Guidelines for Preparation and Research of Ne...
  • 7/24/2023NHC Launches One-Year Campaign to Crackdown on Corruption in Pharmaceu...
  • 7/24/2023CDE Solicits Comments on the Technical Guidelines for Radiolabeled Hum...
  • 7/21/2023US Congressional Panel Raises Concerns Over 'Inadequate' FDA Inspectio...
  • 7/21/2023NMPA Holds the 2023 National Drug Regulatory Work Symposium
  • 7/21/2023NMPA Issues Notice on Revision of Certain Articles of the Provisions f...
  • 7/18/2023NDRC Releases the Draft Industrial Structure Adjustment Guidance Catal...
  • 7/17/2023NMPA Solicits Comments on the Technical Guidelines for Clinical Resear...
  • 7/17/2023NMPA Issues the List of Reference Formulations for GQCE Studies (70th ...
  • 7/17/2023NMPA Announces Additional Professional Journal Approved for Rx Drug Ad...
  • 7/14/2023Snapshot of Import Drugs Approved by NMPA in 2022 (2)
  • 7/11/2023NMPA Issues the Technical Guidelines for Clinical Trials of Human Papi...
  • 7/10/2023NMPA Solicits Comments on the CDE Work Procedures for Safety Informati...
  • 7/10/2023CDE Issues the Principles for the Identification, Management, and Eval...
  • 7/5/2023NMPA and Chinese Customs Announce the Customs Commodity Codes of Oxeli...
  • 7/5/2023NMPA Issues the Provisions on Drug Standards
  • 7/4/2023CDE Publicizes the List of Reference Formulations for GQCE Studies (72...
  • 7/4/2023CDE Issues the Announcement for Applicability of ICH Guideline M10 Q&A...
  • 7/3/2023NMPA Solicits Comments on the Draft Measures for the Supervision and I...
  • 7/3/2023CDE Issues the Guidelines for Acceptance and Evaluation of APIs (Trial...
  • 6/30/2023NMPA Solicits Comments on the Draft Technical Guidelines for Preparing...
  • 6/29/2023NMPA Launches Nationwide Drug Safety Campaign
  • 6/29/2023NMPA Releases Draft Documents Relating to Drug Package Insert Reform
  • Page:7/9 Total number of articles:250: [First][<<] [5] [6] [7] [8] [9] [>>] [End]
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