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International Pharmaceutical Regulatory Monitor
> EMA Updates Guideline on Clinical Investigations of VTE Products
International Pharmaceutical Regulatory Monitor
June 2012
| Vol.
40 No.
6
EMA Updates Guideline on Clinical Investigations of VTE Products
The European Medicines Agency (EMA) has updated its draft guideline on clinical investigations of venous thromboembolism (VTE) products, adding new definitions for bleeding events and secondary endpoints to consider for clinical trials.
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