5thPort

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Digital Patient Engagement and e-Consent Platform for Clinical Trials

5thPort is a patient engagement & eConsent solution that improves drop-out rates, conversion rates, protocol adherence & audits.

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131 Continental Drive, Suite 409,
Newark, DE 19713,
United States of America
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5thPort is a patient engagement and eConsent solution that improves drop-out rates, conversion rates, protocol adherence and audits.

Built to support sponsors, CROs and sites, it is purposefully designed to tackle four primary challenges in site-based, decentralized and hybrid trials:

  • reduce your patient drop-out rates
  • improve your participant conversion rates
  • enhance patient protocol adherence
  • simplify your consent-related audit and regulatory compliance processes

Essentially, 5thPort eliminates any reliance on paper informed consent that could otherwise leave an organization open to litigation caused by lost/altered/incomplete forms.

The 5thPort solution is designed to improve drop-out rates, conversion rates, protocol adherence and audits.
The platform helps organisations avoid litigation by not relying on paper informed consent.
Our digital informed consent system can be signed from any device, at any time and any place.
5thPort allows sites to standardise their e-consent creation and review process at scale using ‘one-and-done’ templates.
Our platform is externally validated and complies with 21 CFR Part 11, EU Annex 11, ICH-GCP and HIPAA standards.

BYOC (Build Your Own Content)

5thPort offers a variety of multimedia content that can be customized. You have a host of options including videos, comprehension testing with teach-back, the ability to flag areas for discussion, surveys, acknowledgements and documents that ultimately lead to a digital informed consent that can be signed from any device, at any time and any place.

You can choose to leverage our library of healthcare videos or load your own. The same goes for uploading your own images, comprehension tests, teach-back quizzes and other interactive elements.

Drive Efficiencies in Your Next Clinical Trial

5thPort gives time back to your overburdened clinical research staff.

Sites are enabled to standardize their eConsent creation and review process at scale by using 5thPort’s ‘one-and-done’ templates. They’re then able to drive efficiencies in a secure manner by distributing these study materials and consent forms to multiple sites, simultaneously. And when instances of re-consenting occur, it can be tracked using 5thPort’s version control tool.

5thPort speaks with other platforms: it easily integrates with other systems (such as EHR, EMR, CTMS etc), allowing you to exchange data seamlessly and build a simplified workflow.

Reduce Compliance Risk

A powerful tool, our One Touch Compliance™ report helps arm yourself with the detailed information you need to eliminate expensive informed consent-related audit findings. Actions taken by staff and study participants in real-time are logged as separate date and time-stamped events, with details on the specific action taken and when the action took place.

5thPort’s version control tool ensures that study participants always interact with the most up-to-date version of an engagement or ICF document.

Our platform is externally validated and in compliance with 21 CFR Part 11, EU Annex 11, ICH-GCP (electronic records and signatures) and HIPAA (security and encryption).

Ready to See 5thPort in Action?

Fill in the enquiry form at the top of this page or drop us a note at Info@5thPort.Com for a quick 15-20 minute demo.

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Address
131 Continental Drive, Suite 409
Newark, DE 19713
United States of America

Email address
Address
Toronto office
15 Allstate Parkway, Unit 320
Markham, Ontario
L3R 5B4
Canada