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  • 7/1/2020CDE Issues the M4 Module 1. Administrative Information and Prescribing...
  • 7/1/2020CDE Issues the Guidelines for Evaluation and Management of Safety Info...
  • 7/1/2020CDE Issues the Guidelines for Clinical Trial Registration and Informat...
  • 7/1/2020NMPA Reports on Crackdown of Fake and Substandard Drugs in 2019
  • 7/1/2020China's First COVID-19 mRNA Vaccine Approved for Clinical Trials
  • 7/1/2020Financial-related Company News in Brief
  • 7/1/2020ObsEva and Yuyuan Bio Announce Submission of Chinese Pre-IND Dossier f...
  • 7/1/2020NMPA Issues Announcement on Drug Registration Fee Standards and Rules
  • 7/1/2020NMPA Issues the Requirements for Drug Record and Data Management (Inte...
  • 7/1/2020CDE Issues the Guidelines for Safety Update Reporting During R&D (Inte...
  • 6/30/2020BeiGene Launches Amgen's XGEVA (Denosumab) in China
  • 6/30/2020Recent Executive Movements
  • 6/30/2020NMPA Issues the Chemical Drug Registration Classification and Dossier ...
  • 6/30/2020NMPA Issues the Biologic Product Registration Classification and Dossi...
  • 6/30/2020NMPA Publicizes the List of Reference Formulations for Generic Drug Eq...
  • 6/30/2020Fitch: No Near-Term Impact on Chinese API Makers as Pharma Supply-Chai...
  • 6/30/2020Ex-USPTO Head, Retired Judge Back China Pharma IP Reform
  • 6/30/2020Helsinn Announces Launch of Oral Formulation of Akynzeo in China
  • 6/30/2020How Data Protection Matters for Pharma Cos in Mainland China? - Ensuri...
  • 6/30/2020China to Initiate Use of a Controversial Covid-19 Vaccine in Its Milit...
  • 6/29/2020Lee's Pharma Gains Chinese Import Approval of Unidrox Prulifloxacin Ta...
  • 6/29/2020CDE Seeks Comments on the Guidelines for Use of GnRH Stimulants in Cli...
  • 6/29/2020Burning Rock and CStone to Co-develop Companion Diagnostics for Pralse...
  • 6/25/2020BeiGene's sNDA of Tislelizumab for Frontline Advanced NSCLC Accepted i...
  • 6/25/2020Boehringer Ingelheim's China-developed CSF Live Vaccine Approved
  • 6/25/2020Sinovac Receives Approval from China for its Quadrivalent Influenza Va...
  • 6/25/2020China's Vaccine Development Enters Phase III Trial
  • 6/25/2020Henlius Biotech Gets NMPA Nod for Denosumab Biosimilar
  • 6/25/2020Chi-Med Announces US$100M Equity Investment by General Atlantic
  • 6/24/2020CDE Solicits Comments on the Technical Guidelines for Clinical Trial o...
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