S.L. 458.35 · Pharmacovigilance Regulations (S.L. 458.35)
S.L. 458.35 Art. 19Procedures to obtain data.
Marketing authorisation holders shall establish procedures in order to obtain accurate and verifiable data for the scientific evaluation of suspected adverse reaction reports. They shall also collect follow-up information on these reports and submit the updates to the Eudravigilance database.