Patient identity
Dedicated fields for full legal name, DOB, and institutional ID reduce the risk of misattributed results and support linkage to electronic health records and employer directories.
Using a consistent Healthcare RADT PWC Form improves data quality, documents informed consent, preserves chain-of-custody for test devices, and reduces transcription errors. Consistent fields make it easier to meet state reporting expectations, defend clinical decisions, and support workplace compliance programs while enabling secure electronic signatures and audit trails.
Clinical teams, occupational health personnel, and administrative staff commonly complete and manage RADT records using this form.
Data from the form is then used by clinicians, employers, compliance teams, and, when required, public health authorities for reporting and follow-up.
Dedicated fields for full legal name, DOB, and institutional ID reduce the risk of misattributed results and support linkage to electronic health records and employer directories.
Clear consent text that explains test purpose, data use, and any sharing with public health or employer systems, including how to withdraw consent if applicable.
Explicit entries for manufacturer, lot number, and expiration date enable rapid response for lot-specific recalls and facilitate adverse event reporting.
Structured result options plus a short guidance line for interpretation and recommended next steps (e.g., confirmatory PCR) to standardize clinical disposition.
Fields for the name, role, and credentials of the person performing the test to document training, accountability, and compliance with institutional policies.
Space for signature, signature method (electronic or ink), date/time, and an audit reference to preserve a verifiable record for compliance and legal review.
| Field | Configuration |
|---|---|
| Identity verification | Email + SMS code or institutional SSO |
| Mandatory fields | Make lot, result, collector required |
| Routing | Auto-send positives to public health |
| Storage | Encrypted archive with access controls |
Choose a platform that supports secure signatures, audit trails, and integrations with records systems.
Notify patient of positive result at test encounter.
Follow company policy for employee case advisories.
Reportable conditions vary; many jurisdictions expect prompt reporting within 24–72 hours.
Report device-related adverse events per FDA guidance promptly.
Start retention clock on signature date for compliance.
| 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 vendor | Varies by vendor | Varies by vendor | Varies by vendor |
| Bulk Send | Yes | Yes | Yes | Yes | No |
| Audit Trail | Yes | Yes | Yes | Yes | Yes |
| HIPAA Compliant | Yes | Yes | Yes | No | No |
A manufacturing employer conducts daily RADT screening for a shift.
A community clinic uses the form for symptomatic walk-ins.