Parties
Identify all contracting entities and responsible individuals, including legal entity names, roles (sponsor, investigator, vendor), and primary contact details for notices and compliance.
A precise Education Study Agreement protects participants, preserves institutional compliance with FERPA and HIPAA where applicable, and documents researcher obligations. It sets expectations for data handling, sharing, and retention while enabling transparent review by IRBs, legal counsel, and administrative offices.
Common users include academic researchers, university legal and compliance offices, K-12 administrators, and external vendors conducting studies under institutional oversight.
Signatories usually include an authorized institutional representative plus the principal investigator or vendor representative; parental or guardian signatures are required for minors under applicable law.
Identify all contracting entities and responsible individuals, including legal entity names, roles (sponsor, investigator, vendor), and primary contact details for notices and compliance.
Describe objectives, methodology, participant selection criteria, locations, instruments used, and expected start and end dates to limit scope creep and establish measurable deliverables.
Specify categories of collected data, permitted uses, data minimization, de-identification steps, and conditions for sharing with third parties to meet FERPA and HIPAA obligations.
Detail the consent process, information given to participants or parents, withdrawal procedures, and whether assent or parental permission is required for minors.
State any payments, reimbursements, or incentives for participants, how funds are disbursed, and tax reporting responsibilities if applicable.
Include procedures for amendments, grounds for early termination, notice periods, and post-termination obligations such as data return or destruction.
| Field | Configuration |
|---|---|
| Authentication | Email link plus optional SMS code for higher assurance |
| Consent Disclosure | Present ESIGN consumer disclosure for consumer-facing studies |
| Audit Trail | Capture IP, timestamp, and signer email for each action |
| Retention Setting | Automatically archive signed PDFs to secure storage |
Confirm that the signing platform supports secure PDFs, detailed audit trails, and the integrations required by your institution.
Use platforms that meet institutional security and compliance requirements and that can produce a tamper-evident executed record for long-term retention.
Submit complete materials before recruitment begins; review timelines vary by board.
Collect signed consents prior to any data collection activities.
Retention periods begin on the effective date or final data collection date.
Schedule annual renewals or continuing review per IRB requirements.
Complete final reporting and data disposition per agreement terms.
Create initial draft and attach protocol documents for internal review.
Obtain written IRB approval before beginning recruitment or data collection.
Complete consent and enrollment per approved procedures and eligibility criteria.
Conduct final analysis, return or destroy data, and file final reports.
| signNow | DocuSign | Adobe Sign | PandaDoc | HelloSign | |
|---|---|---|---|---|---|
| Starting Price | $8/user/mo | $15/user/mo | $14/user/mo | $19/user/mo | $15/user/mo |
| Free Trial | 7-day free trial | Varies by plan | Varies by plan | Varies by plan | Varies by plan |
| Bulk Send | Yes | Yes | Yes | Yes | No |
| Audit Trail | Yes | Yes | Yes | Yes | Yes |
| HIPAA Compliant | Yes | Yes | Yes | No | No |
| Envelope Cap | No envelope cap | 100 envelopes/user/year | Varies by plan | Varies by plan | Varies by plan |