eSignature
Secure electronic signature capture with embedded fields, reusable templates, and an audit trail that records signer actions and timestamps for regulatory records.
In the United States, electronic signatures can meet legal and regulatory requirements when implemented under ESIGN and UETA; life sciences teams should also evaluate HIPAA, FERPA, and institutional policies when handling protected health or student data.
Clinical coordinators prepare consent and regulatory documents, map fields from study databases or CRM records into templates, initiate signature requests, and ensure signed copies are stored in the study record for monitor review and audit readiness.
Regulatory administrators manage retention policies, configure authentication and audit settings, review completed audits for compliance, and coordinate BAAs or contractual requirements with vendors and clinical sites.
Secure electronic signature capture with embedded fields, reusable templates, and an audit trail that records signer actions and timestamps for regulatory records.
Two-way connectivity to synchronize documents, contact data, and signature status between signNow and Freshsales CRM to reduce manual entry and maintain a single source of truth.
Multiple signer authentication options including email, SMS, access codes, and optional identity verification steps suitable for higher-risk consent and agreement workflows.
Immutable audit records for each transaction capturing IP addresses, timestamps, and each action taken during the signing process for compliance reviews.
Create and manage templates with merge fields that populate from CRM records, ensuring consistent document structure across studies and sites.
Trigger signature requests, reminders, and archival actions based on CRM events or API calls to streamline administrative tasks and reduce latency.
Sync templates from Google Docs into signNow, convert inline fields to signature and data fields, and push completed PDFs back to Drive with metadata for study and site identifiers to aid records management.
Link contact and deal records to signature workflows so documents are generated with CRM data, signature statuses update automatically, and signed documents attach to the correct CRM record to support audits.
Automatic archival of completed documents to designated cloud folders with naming conventions tied to study IDs and timestamped versions for consistent backup and retrieval.
RESTful endpoints allow programmatic document creation, signing initiation, and retrieval of completed documents and audit logs for deeper systems integrations.
| Feature | Configuration |
|---|---|
| Reminder Frequency | 48 hours |
| Signing Order Mode | Sequential signing |
| Webhook Endpoint | HTTPS callback URL |
| Document Retention Policy | 7 years |
| API Rate Limit Handling | Queued retries |
For life sciences teams, compatibility with desktop browsers, tablets, and mobile devices is essential for remote site visits, study consent, and administrative approvals.
Ensure IT validates browser versions, mobile OS updates, and network policies before wide deployment so field staff and clinical partners maintain reliable access during patient interactions.
A clinical coordinator generates a consent form template populated from the study database and the patient contact record
Resulting in a time-stamped, auditable consent stored against the patient record for monitors to review.
A procurement user triggers a standardized vendor agreement from a CRM opportunity and routes it to legal and the supplier
Ensures the fully executed contract is attached to the CRM deal and retained per retention policy for inspections.
| Feature | signNow (Recommended) | Freshsales CRM |
|---|---|---|
| HIPAA BAA availability | BAA available | No BAA |
| CRM document attachment | Automatic sync | Manual upload |
| Detailed audit trail | Comprehensive | Basic logs |
| Bulk Send support |
Date of signature
Seven years after study completion
Daily incremental backup
Quarterly export
90 days before deletion