Everything you need to collect regulatory compliant data in pre- or post-market Clinical Investigations.
Clinical Investigations for Medical Devices are as different as the devices are many.
The way you collect data in clinical investigations can highly differ from device to device.
The EDC you select must not only adhere to ISO14155:2020 and other industry requirements, but be flexible when it comes to both features and licensing.
Design custom eCRFs or data forms with automatic rules and validation.
Record adverse events with automatic notifications and live progress tracking.