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.
