Safety reports processing from clinical trials and post-marketing sources

DADA is capable of receiving safety data on your behalf from the public, from health professionals, competent authorities, clinical trials and literature sources, amongst others. The experienced team at DADA will conduct triage of case reports to determine seriousness, enter the data into our pharmacovigilance database, code the medical information according to standardised MedDRA terminology and provide medical review and ongoing surveillance of case reports.