Clinical Safety

Biomapas supports Sponsors in clinical research with the services of high-quality safety data processing, handling and reporting, including:

  • Safety management planning;
  • Adverse Events processing, including recording in Safety Database;
  • MedDRA coding;
  • Narrative writing;
  • Medical data review;
  • SUSARs handling;
  • Aggregate reporting.


For any inquiry regarding our services, please contact Biomapas Business Development team.