3/19/2013SFDA Withdraws Buflomedil from the Chinese Market

3/14/2013SFDA Issues 2012 Annual Adverse Drug Reaction Report

2/22/2013Chinese Court Rules against Bayer over Clinical Trial-Related ADR Clai...

2/7/2013China Jails Seven for Making and Selling Chromium-tainted Medicine Cap...

2/1/2013Pharmaceutical Company Loses CNY 1 Billion after 140-word Weibo Messag...

7/23/2012Four Major Pharma Associations Issue Joint Policy Statement on Counter...

7/13/2012SFDA Issues Statements on EU Investigated Roche Products with Missing ...

7/9/2012Roche Drugs under EU Investigation Trigger Questions in China

6/8/2012SFDA Revises Package Inserts of Lamotrigine HCl and Misoprostol Oral F...

5/31/2012SFDA Releases 2011 Annual Report for National Adverse Drug Reaction Mo...

5/25/2012SFDA: 254 Pharma Producers Used Unsafe Drug Capsules

5/8/2012MOH Issues "Provisions for Clinical Application of Antibacterial ...

5/7/2012SFDA Revises the Package Insert of Orlistat

5/4/2012SFDA Revises the Package Insert of Pioglitazone

3/23/2012China face tough battle against antibiotic resistance

3/22/2012SFDA seeks comments on draft of "Guidelines for Preparing Periodi...

2/27/2012The SFDA Complaint and Reporting Center becomes operational

1/2/2012SFDA issues new rule for food and drug complaint reporting

12/8/2011State Council passes the National Drug Safety Plan (2011-2015)

11/17/2011SFDA issues guidelines for ADR surveillance infrastructure building

11/11/2011SFDA issues alert over increased risk of bladder cancer associated wit...

10/25/2011SFDA issues alert on serious allergic reactions of injectable Thymopep...

9/28/2011SFDA seeks public comments on new rule for food and drug safety interv...

6/1/201111 counterfeiters of Roche's Avastin face severe punishments

5/24/2011SFDA issues the Provisions for Adverse Drug Reaction Reporting and Mon...

4/25/2011SFDA issues 2010 annual ADR report

4/15/2011SFDA issues warning over diphosphonate drugs

3/4/2011SFDA warns about ADRs of weight-loss drug Orlistat

2/9/2011MOH issues new rules to ensure timely reporting of medical accidents

12/2/2010SFDA revises package insert for Levonorgestrel tablets

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