Identification
Full legal name, DOB, medical record or employee ID, and contact details to link the result to the correct person and enable follow‑up.
Using a complete RADT Packet reduces reporting errors, ensures clear patient consent and data handling, and helps meet HIPAA and public‑health reporting expectations. Standardized packets also streamline billing, quality assurance, and audit responses while preserving a clear audit trail for each test event.
Each role should follow applicable institutional policies and state public‑health reporting rules when completing and sharing packet information.
A licensed clinician or delegated clinical staff member documents specimen collection, test result, and clinical interpretation. Their signature attests to proper administration of the RADT and any counseling provided.
The patient or a legally authorized representative provides informed consent and acknowledges result receipt; for minors, a parent or guardian signs and provides contact information for follow up.
Full legal name, DOB, medical record or employee ID, and contact details to link the result to the correct person and enable follow‑up.
Clear patient consent language for testing and data sharing; note if consent was verbal, written, or declined and capture signature/date.
Manufacturer, kit lot number, expiration date, and test device ID to support recalls and quality control.
Result field (positive/negative/invalid), time of result, and clinician interpretation or recommended next steps.
Specimen handling entries, personnel initials, and timestamps when samples are transferred or stored.
Fields for public‑health reporting, employer notification, or EHR import status with required identifiers for each destination.
| Field | Configuration |
|---|---|
| Identity | Use name + DOB required |
| Authentication | Email + SMS code for external users |
| Audit Trail | Capture IP, timestamp, user role |
| Data Export | CSV or HL7-compatible export |
Verify that any chosen platform supports HIPAA (BAA as needed), preserves an unalterable audit trail, and provides export formats compatible with your reporting endpoints.
Report to public health within timeframe mandated by state/local rule.
Notify patient promptly, ideally within 24 hours of positive result.
Enter result to chart same business day for clinical continuity.
Keep packet per retention schedule below; see HIPAA retention rules.
Document recommended confirmatory testing and schedule within guidance windows.
Capture identity and consent before specimen collection.
Time and document collection and kit identifiers.
Record test result and clinician interpretation promptly.
Send required fields to public health and archive packet securely.
| 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 |
A clinic uses the packet to collect consent and link results to EHR
Campus health adds parental consent and FERPA notes for students under 18