Reference:ICH ICH E19 Guideline 2022 6: Difference between revisions
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Latest revision as of 13:50, 16 July 2026
| Document information | |
|---|---|
| Reference | ICH ICH E19 Guideline 2022 |
| Validity area | ICH |
| Scope(s) | G |
| Document name | ICH E19 Guideline |
| Version / Revision | 2022 |
| Status | Current |
| Document type | International guideline |
| Language(s) | EN |
| Description | A SELECTIVE APPROACH TO SAFETY DATA COLLECTION IN SPECIFIC LATE-STAGE PRE-APPROVAL OR POST-APPROVAL CLINICAL TRIALS |
| Official source | Official link |
| Restricted access | No |
| Submitted by | Florian Adragna |
| Contributors | |
| Reference Details | |
|---|---|
| Module | Module 5 — Unit 5.1.2 |
| Scope | G |
| Document part | 6 |
| Language | EN |
| Original entry by | Florian Adragna |
| Contributors | |
| Tags | Adverse event, Monitoring, Sponsor, Investigator safety reporting |
Content
[...] Adverse Event of Special Interest: An event (serious or non-serious) of scientific and medical concern specific to the sponsor’s product or programme, for which ongoing monitoring and rapid communication by the investigator to the sponsor can be appropriate. Such an event might warrant further investigation in order to characterise and understand it. Depending on the nature of the event, rapid communication by the trial sponsor to other parties (e.g., regulators) might also be warranted (based on CIOMS VI; see ICH E2F). [...]
