Routine Pharmacovigilance activities

Routine Pharmacovigilance activities

Bluereg can support you in your routine pharmacovigilance activities for early access program, clinical trials or post-marketing, especially for:

• PV case processing (recordings, database entry, case translation and follow-up)
•  Establish causality assessment for PV cases
• Submission to competent authorities
• Literature review

“All these activities are carried out in full compliance with Good Vigilance Practices and local standards.”