---
title: Medical Device Testing Participant NDA Form Template | Paperform
description: Comprehensive confidentiality agreement for medical device clinical trial participants. Protect device data, enable adverse event reporting, and document study compensation with this professional NDA template.
url: "https://paperform.co/templates/medical-device-testing-participant-nda"
type: static
generatedAt: "2026-03-28T00:44:28.343Z"
---

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### Medical Device Testing Participant NDA Form

Conducting clinical trials for medical devices requires careful management of participant confidentiality agreements. This **Medical Device Testing Participant NDA template** helps research organizations, medical device manufacturers, and clinical trial coordinators establish clear confidentiality expectations with study participants while protecting proprietary device information and trial data.

#### Why medical device trials need specialized NDAs

Unlike standard non-disclosure agreements, medical device testing requires balancing participant safety rights with the protection of proprietary technology and unpublished research data. Participants need clear guidance on what information must remain confidential, how adverse events should be reported, and what compensation they'll receive—all while ensuring they understand their rights and obligations.

This form template addresses the unique requirements of medical device clinical trials by combining confidentiality provisions with adverse event reporting procedures and transparent compensation details, creating a comprehensive agreement that protects both the study sponsor and participant interests.

#### Who benefits from this template

This template is designed for:

 - **Medical device manufacturers** conducting pre-market clinical trials
 - **Contract research organizations (CROs)** managing multi-site device studies
 - **Clinical trial coordinators** at hospitals and research institutions
 - **Biotech startups** testing prototype medical devices
 - **University research departments** conducting device feasibility studies
 - **IRB administrators** ensuring proper participant documentation

#### Key features for device trial confidentiality

The form captures essential information including participant demographics, study understanding confirmation, specific confidentiality obligations regarding device specifications and performance data, adverse event reporting procedures, compensation details, and digital signature capture for legally binding acknowledgment.

Conditional logic ensures participants receive appropriate information based on their study role and compensation structure, while required fields guarantee no critical documentation is missed before enrollment proceeds.

#### Streamline your clinical trial workflows

Once a participant submits this NDA, **[Stepper](https://stepper.io)** can automate your entire enrollment workflow: send the signed agreement to your trial management system, create participant records in your CRM or database, schedule orientation appointments, trigger follow-up emails with study protocols, and notify the principal investigator and study coordinator team. You can also use **[Papersign](https://papersign.com)** to collect additional signatures from legal guardians, co-investigators, or compliance officers if your protocol requires multiple sign-offs.

With Paperform's SOC 2 Type II compliance and secure data handling, you can trust that sensitive participant information and proprietary device data remain protected throughout the trial lifecycle. Built-in calculations handle compensation automatically, while professional design ensures participants have a clear, trustworthy experience from first contact.
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