Adverse Event Intake

Highly Experienced Staff with Expertise in Global Adverse Event Data Collection

As a pharmacovigilance (PV) provider and medical information contact center, ProPharma Group understands what our clients need from adverse event (AE) data collection. We intake nearly 100,000 AEs per year and understand the importance that each data element collected has on case assessments for seriousness and expectedness, as well as other aspects of AE management. It may be the only opportunity to speak with the reporter so it is critical to get as much information as possible on the initial contact.

Our highly-trained staff follow established processes and guidelines to obtain as much AE information as possible. That comprehensive AE data is documented in our database and the AE case records are sent to the client’s pharmacovigilance department within one business day. We also offer clients the option for ProPharma Group to execute outbound follow-up communication to collect additional data that was not available at initial intake, lessening the burden on their internal pharmacovigilance department.