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Pharmacovigilance Management
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Global Reporting Assessments
Pharmacovigilance Consulting
 

GLOBAL REPORTING ASSESSMENTS
International regulations for clinical trials safety and post-marketing pharmacovigilance require expertise and creativity in order to respond to the initiative of Volume 9A including electronic reporting (E2B), and Qualified Persons for Pharmacovigilance (QPPv) for our complex safety environment. DSA can assess and prepare your international regulatory reports and also help you navigate the complex environment abroad. Ask the drug safety experts about going global.

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