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Overview
Results of the early benefit assessment
G-BA procedures
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Patients
Procedures without a dossier
Indication areas (G-BA)
Eye diseases
Skin diseases
Cardiovascular diseases
Infectious diseases
Respiratory system diseases
Hematopoietic diseases
Musculoskeletal system diseaeses
Nervous system diseases
Genitourinary system diseases
Digestive system diseases
Oncological diseases
Mental illnesses
Other diseases
Metabolic diseases
Orphan Drugs
Special marketing authorisations
Orphan drugs
PUMA
ATMP
ATMP CAR-T cells
Conditional marketing authorisation
Approval under exceptional circumstances
Accelerated assessment
Evidence transfer
Results of reassessments
Limitation
G-BA request (§13 VerfO)
Manufacturer's request (§14 VerfO)
Orphan drugs, turnover exceeding €50m
Orphan drugs, loss of status
G-BA requirements
Collection of routine practice data (AbD)
Quality requirements for ATMP
Bundling
Revocation of the resolution
Procedures
Resolutions
Active procedures
Arbitrations
Reimbursement prices
Recent price changes
Discontinuations
Special practice conditions
Exclusions from prescription
Changes in legal regulations
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Interactive analysis: dimensions
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AMNOG Monitor app
Calculation methods
Arbitration board
Endpoints Quality of Life
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Monthly report
Einzelauswertungen
Interactive analysis
Interaktive Auswertung: Datenexport Excel
Interactive analysis: dimensions
Intelligent search
AMNOG Monitor app
Calculation methods
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