Clinical Trials
Atessia Vigilances manages the pharmacovigilance of phase II, III and IV clinical trials in compliance with regulatory requirements, ensuring the quality and safety of your pharmacovigilance data.
- Manage SAEs and SUSARs, from reception to submission to health authorities and CPPs / Ethics Committees
- Request clarifications or queries from investigators
- Write and send Dear Investigator Letters
- Write DSURs
- Participate in the writing, proofreading, and commenting on protocols
- Carry out unblinding
