patinet-using-electronic-digital-medical-consent-australia

Why Consentic

Consentic supports doctors and health care practitioners to explain and consent patients to their procedure, treatment or clinical trial.

Consentic standardises your consent process, offering medicolegal protection, whilst saving time and giving you peace of mind.

Every 5 minutes we facilitate one informed consent in Australia.

What does Consentic do?

Consentic provides a suite of comprehensive yet informative and easy to understand medical explanations, in the form of peer reviewed animations, or illustrated PDFs.

Patients can be emailed, SMS’d or complete the consent on site, prior to answering questions agreeing to the risks of the procedure/treatment or clinical trial, before electronically signing a consent form. This is stored in the patient’s electronic medical record.

What are the features of Consentic?

  • Peer reviewed medical explanations, or bespoke content
  • Automated follow-ups and tracking to help you manage patient communications
  • Ability to email or sms consents to patients
  • Peer reviewed medical explanations, or bespoke content
  • Automated follow-ups and tracking to help you manage patient communications
  • Ability to email or sms consents to patients
  • Can be integrated into practice management software
  • Medicolegally designed to help you and your practice meet and exceed the required standard of care
  • Content for patients from culturally and linguistically diverse backgrounds
  • Can be integrated into practice management software
  • Medicolegally designed to help you and your practice meet and exceed the required standard of care
  • Content for patients from culturally and linguistically diverse backgrounds
  • Peer reviewed medical explanations, or bespoke content
  • Automated follow-ups and tracking to help you manage patient communications
  • Ability to email or sms consents to patients
  • Can be integrated into practice management software
  • Medicolegally designed to help you and your practice meet and exceed the required standard of care
  • Content for patients from culturally and linguistically diverse backgrounds

How Consentic Works

informed consent

STEP 1

The consent video/form is selected for the patient’s procedure or clinical trial. Any risks specific to that patient can be documented on the platform by the clinician, and additional information can be uploaded.

informed consent

STEP 2

The patient watches the animation or reads the form relevant to their procedure. At any time, patients can pause, rewind and repeat any section of the video. The patient can be emailed a link to watch the video from home.

informed consent

STEP 3

The patient is prompted to complete questions about the procedure/clinical trial that highlight specific risks. Patient queries are alerted to the clinician.

informed consent

STEP 4

The consent is signed by the patient and the clinician. This is emailed to a practice/study site and loaded into the patients medical record. The consent form is securely stored on the platform, protecting you now and into the future.

How Consentic Works

informed consent

STEP 1

The consent video/form is selected for the patient’s procedure or clinical trial. Any risks specific to that patient can be documented on the platform by the clinician, and additional information can be uploaded.

informed consent

STEP 2

The patient watches the animation or reads the form relevant to their procedure. At any time, patients can pause, rewind and repeat any section of the video. The patient can be emailed a link to watch the video from home.

informed consent

STEP 3

The patient is prompted to complete questions about the procedure/clinical trial that highlight specific risks. Patient queries are alerted to the clinician.

informed consent

STEP 4

The consent is signed by the patient and the clinician. This is emailed to a practice/study site and loaded into the patients medical record. The consent form is securely stored on the platform, protecting you now and into the future.

FEATURES

  • Compatible with all browsers
  • Audit trails to track activity, confirming patient has received, opened information and signed
  • Intuitive, and easy to use
  • Encrypted data in transit and at rest
  • Integratable with practice management software
  • CFR Part 11 compliant
  • All data in line with relevant data protection laws
informed consent