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.”

 

pharmaco-organisations-1

Discover our last white Paper

Learn more