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4.3 Key subgroups
5. The 9-month all-oral regimen
5.1 Eligibility
5.2 Composition and duration of the regimen
5.6 Using modified all-oral shorter MDR-TB regimens under operational research
9.1 Policy and operational documents
9.2 National MDR-TB expert committee or technical working group
9.3 Electronic recording and reporting
9.4 Estimates (epidemiological and logistics)
9.5 Management of the supply chain and storage conditions for pharmaceuticals
10.1 Treatment outcome definitions
4.2.2 BPaL regimen
4.2.3 Duration of treatment
7. Supporting people in adhering to and completing TB preventive treatment
5.4.1 DST results
5.4.2 Patient subgroups
6. The longer regimens
6.1 Eligibility
6.2 Composition and duration of the regimens

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