Privacy Policy
Last updated: July 9, 2026
1. Introduction
Lynd Clinical, Inc. (“Lynd Clinical,” “Lynd,” “we,” “us,” or “our”) provides a clinical-trial participant recruitment, screening, and electronic-signature platform used by research sites, investigators, and study sponsors. This Privacy Policy explains how we collect, use, disclose, and protect information when you:
visit our website at lyndclinical.com (the “Website”);
use the Lynd platform (the “Platform”); or
receive communications from us, including email, telephone calls, and text (SMS) messages (collectively with the Website and the Platform, the “Services”).
This Privacy Policy describes how we handle your information. By using the Services, you acknowledge that you have read and understand this Policy.
2. Our Role and Health Information (HIPAA)
While the information that you provide to us may not be subject to regulation under federal health privacy laws, certain of the health information in the Services may be deemed to be Protected Health Information (“PHI”) that belongs to, and is provided by, the research sites and their affiliated healthcare providers (collectively, the “Research Sites”) who use Lynd. The Research Sites that provide this information to Lynd Clinical are the covered entities under the Health Insurance Portability and Accountability Act (“HIPAA”). Lynd Clinical may process the information on their behalf as a Business Associate under HIPAA. . Our handling of this PHI is governed by our Business Associate Agreements (“BAAs”) with those organizations, and where a BAA conflicts with this Policy as to PHI, the BAA controls.
For information you provide to us directly — such as when you visit our website, contact us, or consent to receive text messages — or information that we receive via your HIPAA-compliant authorization, Lynd Clinical determines how that information is handled, as described in this Policy and as described in the terms of any applicable authorization.
HIPAA and consent to receive messages are separate. Authorizing the use or disclosure of your health information (a HIPAA authorization) is not the same as consenting to receive text messages, and consenting to receive text messages is not a HIPAA authorization. Each is requested separately, and you may decline or withdraw either one.
3. Information We Collect
Depending on how you interact with us, we may collect the following categories of information:
Identifiers and contact information — name, email address, telephone/mobile number, mailing address, and, for participants, date of birth and medical record number (MRN).
Health information — medical history, diagnoses (e.g., ICD-10 conditions), laboratory and imaging results, medications, allergies, encounter history, and demographic and eligibility details.
Screening and eligibility information — responses to study screening questionnaires and related recruitment status.
Consent and communication records — your contact-method consents (including SMS opt-in/opt-out), HIPAA authorization records, and the date, method, and content of disclosures you were shown.
Electronic-signature records — your electronic signature, the document and its version, the meaning of the signature, and the date, time, IP address, and device/browser used to sign.
Eligibility assessments — match scores, rationales, and related output generated by our software to support recruitment decisions.
Audit and security records — an append-only audit trail of actions taken in the Services, attributable to the acting user.
Technical and usage data — IP address, browser/device information, and log data generated when you use the Website.
4. Cookies and Tracking Technologies
Our Website uses cookies and similar technologies such as tracking pixels and web beacons (collectively referred to as “cookies”) to collect user activity information, including your browsing activities and preferences. We may use the following types of cookies:
Performance and Functionality Cookies. These cookies are used to enhance the performance and functionality of our Websites but are nonessential to their use. However, without these cookies, certain functionality (like videos) may become unavailable.
Analytics and Customization Cookies. These cookies collect information that can help us understand how our Website is being used. This information can also be used to measure effectiveness in our marketing campaigns or to curate a personalized Site experience for you.
Advertising Cookies. These cookies are used to make advertising messages more relevant to you. They prevent the same ad from continuously reappearing, ensure that ads are properly displayed for advertisers, and in some cases select advertisements that are based on your interests.
Social Networking Cookies. These cookies enable you to share our Website’s content through third-party social networks and other websites. These cookies may also be used for advertising purposes.
Some internet browsers have “Do Not Track” or “DNT” features which, when turned on, send a signal to a website that the individual visiting the website does not wish to be tracked. Such browser features and industry standards are not uniform, so our Website does not respond to DNT signals, but you can control your cookie preferences in the settings of your Internet browser. Please note that if you block or reject cookies on our Website, some functionality of the Website may be limited.
5. Mobile Information and Text Messaging (SMS)
This section describes how we handle information related to our text-messaging program. It is incorporated into, and is part of, this Privacy Policy.
What we collect and why. With your consent, we collect your mobile phone number to send you one-time verification and signing codes that confirm your identity when you electronically sign clinical-trial documents. Where you have separately opted in, we may also send service notifications such as appointment or study reminders. We do not send marketing text messages.
No protected health information is sent by SMS. Our text messages contain only the information needed to complete the action (for example, a numeric code) and never include your name, date of birth, MRN, diagnosis, or other health details.
We do not share or sell your mobile information. The following statement is a core commitment of our messaging program:
No mobile information will be shared with third parties or affiliates for marketing or promotional purposes. Text messaging originator opt-in data and consent will not be shared with any third parties.
We do not sell, rent, or trade your mobile phone number or your SMS opt-in/consent data. We use a trusted messaging service provider (a Communications-Platform vendor) solely to deliver messages on our behalf; that provider processes your mobile number only as needed to transmit our messages and is contractually prohibited from using it for any other purpose.
Consent. We send text messages only after you opt in (for example, by checking a clearly labeled, un-pre-selected box and providing your mobile number, or by texting a keyword to us). Consent to receive text messages is not a condition of any treatment, payment, enrollment, or participation in a study.
Frequency and cost. Message frequency varies; verification codes are sent only when you request to sign a document. Message and data rates may apply.
Opting out and getting help. You can opt out at any time by replying STOP to any of our messages; we will send a single confirmation and then stop sending messages to that number. Reply HELP for help, or contact us at privacy@lyndclinical.com. Opting out of text messages does not opt you out of email or other communications, which you can manage separately.
See our Terms of Use for the full SMS program terms.
6. How We Use Information
We use information to:
verify identity and deliver one-time signing/verification codes;
provide, operate, maintain, and secure the Services;
support participant recruitment, screening, and electronic signing on behalf of Research Sites and sponsors;
send service communications you have requested or consented to;
comply with legal, regulatory, and recordkeeping obligations, including applicable requirements under 21 CFR Part 11 and FDA recordkeeping rules; and
detect, investigate, and prevent fraud, abuse, and security incidents.
7. How We Share Information
We share information only as follows:
With the Research Sites, investigators, and sponsors for whom we process the information, consistent with our agreements and applicable law.
With service providers and subprocessors who perform services for us — for example, cloud hosting, transactional email delivery, telephony, and SMS delivery — under contracts that require them to protect the information and use it only to provide services to us.
For legal and safety reasons — to comply with law, regulation, legal process, or enforceable governmental request, or to protect the rights, property, or safety of Lynd, our users, or others.
In a business transfer — in connection with a merger, acquisition, financing, or sale of assets, subject to this Policy.
We do not sell your personal information, and — as stated in Section 5 — we do not share mobile opt-in data or consent with third parties, and we do not share mobile information with third parties or affiliates for marketing or promotional purposes.
8. How We Protect Information
We maintain administrative, technical, and physical safeguards designed to protect information, including:
encryption in transit (TLS/HTTPS) and encryption at rest;
network isolation of our databases (no public network exposure);
unique, named user accounts with multi-factor authentication required for production access, role-based least-privilege authorization, and organization-level tenant isolation;
an append-only audit trail recording actions on records; and
session controls, access reviews, and timely deprovisioning.
No method of transmission or storage is completely secure, and we cannot guarantee absolute security.
9. Data Retention
We retain information for as long as needed to provide the Services and to meet our legal, regulatory, and contractual obligations. Clinical records and their audit trail are retained in accordance with applicable regulatory requirements — including the requirement under the FDA regulations (21 CFR 312.62(c)) that require clinical-trial records to be kept for at least two years after a marketing application is approved (or after the investigation is discontinued) — and for any longer period required by the sponsor or protocol. Mobile numbers and SMS opt-in/consent records are retained for as long as your consent is active and as required to evidence consent and comply with law. We do not destroy clinical records before their retention period elapses.
10. Your Choices
Text messages: opt out anytime by replying STOP; reply HELP for help.
Email: use the unsubscribe link in our emails or contact us.
Access, correction, and deletion: because much of the health information we process was provided by – and remains under the control of – the research site or provider conducting the study, requests to access, correct, or delete that information may need to be directed to that organization; we will assist as required by our agreements and applicable law. For information you provided to us directly, contact us using Section 14.
HIPAA rights: you may have rights regarding your PHI (including the right to revoke a HIPAA authorization in writing); contact the research site or other healthcare provider that holds your records.
11. AI/Automated Processing
Lynd uses artificial intelligence and machine learning tools to help identify individuals who may be potentially eligible to participate in clinical trials. As part of this process, our AI model analyzes certain categories of personal data, which may include [categories of personal data used as inputs, e.g., demographic information, health-related data, geographic location, prior treatment history, and other relevant criteria]. These tools assist our team by generating preliminary assessments of potential eligibility; however, all outputs produced by the AI model are advisory in nature only. No decision regarding an individual's eligibility or participation in a clinical trial is made solely on the basis of automated processing. A qualified human investigator or other authorized personnel reviews all AI-generated outputs and makes the final determination before any action is taken with respect to an individual.
If you are a resident of a jurisdiction in the United States that provides rights related to automated decision-making, you may have the right to request meaningful human review of any decision that was significantly influenced by automated processing, to object to the use of automated processing with respect to your personal data, or to request a further explanation of the logic and criteria used in reaching a particular result. To exercise any of these rights, or if you have questions about how our AI tools process personal data, please contact us using the information provided elsewhere in this Privacy Policy. We will respond to your request in accordance with applicable law.
12. U.S. State Privacy Rights
Depending on where you live, state privacy laws may give you certain rights over the personal information we collect about you. These rights may include the right to:
Access the personal information we hold about you and request a copy of that information in a portable, readily usable format;
Correct inaccurate personal information we maintain about you;
Delete personal information we have collected from or about you, subject to certain exceptions;
Opt out of the sale or sharing of your personal information, if applicable; and
Limit how we use and disclosure certain personal information.
It is important to understand that certain of the health-related information collected and maintained through our Services is regulated under HIPAA or is used in connection with regulated clinical research. HIPAA provides its own comprehensive framework of privacy rights and protections for this type of information — including rights of access, amendment, and restrictions on how your health information may be used and disclosed. Because these protections already apply under federal law, information that is covered by HIPAA or associated with regulated clinical research is generally exempt from, or treated differently under, state privacy laws. This means that the state-based rights described above apply only to personal information that falls outside the scope of HIPAA and regulated clinical research activities.
To exercise any applicable rights, contact us using Section 14. We will not discriminate against you for exercising your rights.
13. Children’s Privacy
The Services are intended for use by adults (18+) and by authorized professional users. We do not knowingly collect personal information directly from children through the website. Where a study involves minors, information is provided through the Research Site and the minor’s parent or legally authorized representative, consistent with the applicable consent and authorization.
14. Changes to This Policy
We may update this Privacy Policy from time to time. We will post the updated version here and revise the “Last updated” date above. Material changes to our SMS practices will be reflected here and, where appropriate, communicated to you.
15. Contact Us
Questions about this Privacy Policy or our data practices:
Lynd Clinical, Inc.
817 Broadway, 7th Floor
New York, NY 10003
Email: privacy@lyndclinical.com