TELOS-C can provide EUQPPV (as per EU directives) and the pharmacovigilance local contact person (as per Belgian regulation) for any clinical trial and postmarketing activities conducted within the European Union.
SAE Reconciliation:
For Serious Adverse Events (SAE), we offer medical coding services and performs SAE reconciliation between pharmacovigilance data and CRF data.
Literature review:
Our company has extensive experience in literature review required in the frame of pharmacovigilance activities.
Training:
With over 20 years of expertise in pharmacovigilance, we offer efficient training to external personnel.