Clinical trial compliance: Turn your consent form tracking nightmares into eConsent dreams.
Incomplete, incorrect and outdated informed consent forms not only pose risks to the integrity of your clinical study, but also demand substantial time and effort to rectify. This can pose problems with clinical trial compliance.
5thPort’s digital patient engagement and eICF (electronic informed consent form) solution challenges these issues head on, enabling you to achieve the highest standards of clinical trial compliance with powerful accuracy.
eConsent is the future. Rely on paper no more.
Gone are the days of numerous informed consent form paper copies circulating within your trials. With 5thPort you will be sure of:
- Streamlined digital consent workflows and monitoring
- Real-time access to eConsent historical data
- Trackable record-keeping of every patient/staff interaction on an Informed Consent Form
- Informed Consent Form version control
- Strict access permissions/credentials