AE-Connect 5.8 (Adverse Event/Side Effect Reporting Form Collection Management)
Electronically collect side effects and adverse events (safety information) using mobile devices to improve the situation of MR!
AC-Connect: A new standard for collecting adverse event information that balances accuracy and speed, making adverse event reporting smarter. 'AE-Connect' is a system that allows medical representatives (MRs) to quickly and reliably report safety information obtained to the pharmacovigilance (PV) department using a smartphone. When an MR obtains information about an adverse event at a facility, they can input the necessary information for the initial report through the web browser on their mobile device. The initial report from the MR is immediately displayed in a list on the management screen of the safety management department (PV department), where detailed information can be confirmed. Additionally, inquiries to the MR can be made as needed. Furthermore, new information can be added as supplementary information to previously reported data. 【Features】 ■ Streamlines the time of busy MRs ■ Maintains the accuracy of reported information, allowing the PV department to receive it in a normalized and structured state through input validation features ■ Achieves data linkage with other systems using an industry-standard (E2B) interface (XML linkage) ■ Retains activity records between MRs and PV, as well as audit trails of collected data, ensuring compliance with regulations ■ Allows files to be attached to contact report information, enabling centralized management of information related to the contact report *Please feel free to contact us.
- Company：d-Solutions
- Price：Other
