This application view consolidates identifiers, linked product and market authorization context, dossier structure, sequence history, and active authority obligations in one place. Regulatory teams use it to understand readiness and risk before publishing new sequences or responding to open questions. Cross-links to labeling and variations maintain lifecycle traceability for post-approval changes. Inspection readiness risk is calculated from overdue commitments, failed sequences, and unresolved high-risk correspondence for immediate action.

Application ID
APP-031
Application Number
TFDA-2024-0031
Procedure Type
sBLA
Status
Draft
Linked Product
Market Authorization
United States · TFDA
Dossier Structure View
DossierFormatVersionModulesModule BreakdownStatus
DOS-031NeeS5.3.85M1 (12), M2 (15), M3 (12), M4 (10), M5 (7)Draft
Sequence Timeline
2024-04-17
0031 · Type IA Variation
Status: active. ACK: 2024-05-10.
2023-10-29
0131 · Type II Variation
Status: active. ACK: 2023-12-10.
2023-09-11
0231 · Type II Variation
Status: in-progress. ACK: pending.
2023-07-16
0331 · Safety Update
Status: active. ACK: 2024-03-24.
Open Questions and Commitments
QuestionDue DateRiskStatus
Request for updated SmPC section 4.12025-02-12mediumOpen
Request for updated SmPC section 4.12025-03-26lowOverdue
Request for benefit-risk assessment addendum2024-12-30mediumIn Progress
Linked Labeling and Variations
Labeling ArtifactTypeVersionStatus
LBL-091IFU19.5In Progress
LBL-092IFU8.4Active
VariationTypeStatusSubmitted
TFDA-2024-0031-V031MajorCompleted2023-06-16
TFDA-2024-0031-V131MinorPending2023-09-08
TFDA-2024-0031-V231MajorDraft2023-12-12
TFDA-2024-0031-V331Type IIDraft2023-12-03
TFDA-2024-0031-V431Type IICompletedpending
Inspection Readiness Risk Panel
Risk Score: 2 · Overdue commitments: 1, failed/blocked sequences: 0, high-risk questions: 0.
Recommended next step: resolve outstanding questions and commitments before next publishing cycle to reduce inspection exposure.