Description
Identify a supplied clinical-research reconsent version.
Clinical-research records connect source fields, protocol dates, training, signatures, safety communications and consent versions. A recorded acknowledgment or date predicate does not establish valid consent, authorized delegation or compliance. Source documentation and substantive participant protections require separate review.
Identify a supplied clinical-research reconsent version.
When to use this tool
Use GCP Reconsent Version Label when checking the stated benign clinical-research record or date convention.
How to use the tool and how it works
- Enter participantId, consentVersion, reconsentRecordId. Use the units and conventions below.
- Run the tool. Correct any format, range, or cross-field input error before interpreting the output.
- Read token. Use the output convention below.
Require nonempty participant ID, consent version and reconsent-record ID. Encode the ordered triple as JSON text.1
| Input field | Meaning and units | Accepted input |
|---|---|---|
| participantId | Participant Id | Required. Text; minimum UTF-16 length 1; maximum UTF-16 length 8192. |
| consentVersion | Consent Version | Required. Text; minimum UTF-16 length 1; maximum UTF-16 length 8192. |
| reconsentRecordId | Reconsent Record Id | Required. Text; minimum UTF-16 length 1; maximum UTF-16 length 8192. |
| Output field | Interpretation | Returned shape |
|---|---|---|
| token | JSON-encoded ordered tuple or literal token under the convention above; not a database lookup or authentication result. | Required. Text; maximum UTF-16 length 8192. |
{
"input": {
"participantId": "P17",
"consentVersion": "v2",
"reconsentRecordId": "RC2"
},
"output": {
"token": "[\"P17\",\"v2\",\"RC2\"]"
}
}Limitations and assumptions
- No consent document is inspected and valid informed consent, actual reconsent or participant understanding is not established.
- Inputs must satisfy both the field types and the cross-field conditions above. Invalid input causes an error; a successful false flag or documented placeholder is a different result.
Alternative or Complementary methods
Review verified protocols, consent and source records under the applicable complete research requirements with qualified responsible personnel for actual study or participant decisions.
References
Similar or alternative tools
- GCP Safety Letter Receipt Code
Record receipt of a clinical-study safety communication using a supplied code.
- GCP Signature Authority Role
Record the stated authority role attached to a clinical-research signature.