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-009
Application Number
SwissMedic-2021-0009
Procedure Type
MAA
Status
In Progress
Linked Product
Market Authorization
Switzerland · SwissMedic
Dossier Structure View
DossierFormatVersionModulesModule BreakdownStatus
DOS-009CTD2.2.25M1 (5), M2 (12), M3 (7), M4 (6), M5 (4)Active
Sequence Timeline
2023-10-06
0009 · Annual Report
Status: active. ACK: 2023-06-23.
2023-07-12
0109 · Renewal
Status: failed. ACK: 2023-11-02.
2023-06-25
0209 · Annual Report
Status: approved. ACK: pending.
2023-03-03
0309 · Urgent Safety Restriction
Status: blocked. ACK: pending.
Linked Labeling and Variations
Labeling ArtifactTypeVersionStatus
LBL-025IFU19.8In Progress
LBL-026PIL20.2In Progress
VariationTypeStatusSubmitted
SwissMedic-2021-0009-V009Type IBActive2024-01-18
SwissMedic-2021-0009-V109Type IIDraftpending
SwissMedic-2021-0009-V209MinorFailed2022-08-20
SwissMedic-2021-0009-V309MajorSubmitted2023-12-30
SwissMedic-2021-0009-V409Type IABlocked2023-04-04
Inspection Readiness Risk Panel
Risk Score: 8 · Overdue commitments: 2, failed/blocked sequences: 2, high-risk questions: 0.
Recommended next step: resolve outstanding questions and commitments before next publishing cycle to reduce inspection exposure.