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Pharmacovigilance

Altizem offers you the entire management of Serious Adverse Events of your national and international trials.

Expertise

Training and support of site investigator for the management of Adverse Events and Serious Adverse Events
Collection, processing and sending notification to health authority of Serious Adverse Events.
Risk Management plan.
Notification to Ethic Committee.
Writing of reports and narratives.
Follow-up and reconciliation of pharmacovigilance and clinical databases.