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Regulatory News
 
CDE Solicits Public Comments on Six TCM Technical Guidelines 4/13/2017
CFDA Issues New Announcement (2017#42) for Clinical Data Self-Ins... 4/13/2017
Summary of Drug Registration Evaluation and Approval in the Past ... 4/12/2017
CFDA Solicits Comments on 2nd Draft of Document for Handling of C... 4/10/2017
CFDA and NHFPC Publish Their 2017 Budgets 4/7/2017
CDE Accepted 871 Drug Registration Applications in Q1/2017 4/7/2017
NHFPC, CFDA Issue Joint Notice to Strengthen Filing and Regulatio... 4/6/2017
CFDA Issues Document for Product Classification under Generic Dru... 4/5/2017
CFDA Announce Decision to Adjust Certain Drug Approval Processes 4/5/2017
NPC to Undertake Inspection of Drug Administration Law Enforcemen... 4/3/2017
CFDA Terminates Collection of Numerous Fees 3/31/2017
Pharma Industry Reform to Focus on First-to-copy Drugs and Import... 3/30/2017
CDE Seeks Comments on 2nd Draft of Phase I Trial Guidelines 3/29/2017
CFDA Holds National Drug Registration Conference, Highlighting Va... 3/27/2017
CFDA Issues Announcement for Package Insert Revision of Nicotine ... 3/23/2017
Review of Chinese Drug Evaluation and Registration in 2016 3/22/2017
CFDA Announces Outcome of Past Policy Cleanup 3/22/2017
State Council Amends Radioactive Drug Regulation, Liberalizing It... 3/22/2017
Ex-manufacturer Drug Price Tracing Policy Expected To Be Released... 3/22/2017
CFDA Releases List of Reference Formulations for Generic Drug Equ... 3/20/2017
CFDA Terminates Import of OM Pharma's Broncho-Vaxom 3/20/2017
CFDA Solicits Comments on Proposed Policy to Liberalize Import Dr... 3/17/2017
CFDA Releases Biochemical Drug Appendix of 2010 GMP 3/17/2017
CFDA Releases List of Reference Formulations for Generic Drug Equ... 3/17/2017
Snapshot of CFDA Approved Imported Drugs in 2016 3/16/2017
CFDA Issues New Rules for Drug Evaluation Expert Committee 3/9/2017
CFDI Announces Inspection Plan for Overseas Pharma Facilities in ... 3/9/2017
CFDA Minister Responds to Delayed Access to New Drugs 3/7/2017
CFDA Announces Designation of 12 Clinical Trial Institutions 3/6/2017
CFDI to Initiate Clinical Data Inspection of 32 Drug Products 3/6/2017
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