Free Newsletter
Regulator investigates Nanjing plant
China's State Food and Drug Administration (SFDA) is investigating quality concerns at a Simcere Pharmaceutical Group (NYSE: SCR) plant in Nanjing. Production operations were suspended by the drugmaker's subsidiary, Jiangsu Yanshen Biological Technology, at the end of November.
At issue is the manufacturing of a human use rabies vaccine (vero cell). Four batches made between July and October 2008 "have been found to have quality problems," the company says in an announcement. Further details are currently unavailable.
The regulator ordered the drugmaker to halt marketing and production of all products made at the facility, including the human use rabies vaccine, "and has organized experts to provide an assessment of risks presented by the problem vaccine."
The week prior to the start of the SFDA investigation, Simcere says it had urged the board of Jiangsu Yanshen to replace its general manager and head of quality assurance. The internal suspension of operations followed.
- see the Simcere announcement
Related Articles:
China revising GMPs
Courses target Chinese drug makers
Paid Research Reports
- Trends in mHealth and Telemedicine
- The Global Aesthetic Dermatology Market Outlook
- Future Directions in Regenerative Medicine
- Pipeline Insight: Insulin Antidiabetics – Novel analogs show promise as alternative delivery methods prove less attractive
- Pipeline Insight: Non-insulin Antidiabetics - Rise of the weight-reducers: Once-weekly GLP-1 agonists and novel SGLT-2 inhibitor
- Forecast Insight: Antidiabetics - Diabetes market growth driven by epidemiological trends and rich pipeline

SHARE
WITH: