- Redmine:
    - fix/renew expired certificate

- Schedule:
    - Finalise and update upper/lower visit windows
    - d1:
        - "Urine will be tested on day 1 with a lateral flow tuberculosis (TB) lipoarabinomannan (LAM) assay"
        - "Bloods will be drawn on day 1 to assess serum creatinine, full blood count with differential (FBC) and alanine transaminase (ALT) levels"
    - d14
        - "Bloods drawn to check FBC and differential count"

- SAE CRF:
    - validate Flucytosine only applicable if it is a study drug (i.e. on that arm of trial)
    - if hospitalized
        - Lab CRF
        - Clinical Assessment CRF

- TMG Form:
    - should Original Report be read only?

- Death CRF:
    - reconcile with provided CRF (09_Death_Form_110821_V0.5.pdf)
    - if death, required:
        - SAE CRF
        - Death CRF
        - Termination CRF
        - Adherence
        - Clinical Assessment CRF

- Requisitions:
    - combine renal (RFT) and liver (LFT) function tests into single requisition
        - combine results forms

- Subject visit:
    - Hide 'survival_status' at baseline
        - trigger AE_INITIAL_ACTION/DEATH_REPORT_ACTION if answer YES to 'survival_status'
    - Hide 'hospitalized' at baseline
        - trigger AE_INITIAL_ACTION if answer YES to 'hospitalized'

- Study Medication CRF:
    - capture initial prescription
    - capture time_of_first_dose ???[4am, 10am, 4pm, 10pm]
    - capture modifications at subsequent visits (e.g. "Were there modifications to the study medication?")

- Signs and Symptoms CRF:
    - look at basic validation for _sx_other fields

- Mental Status CRF:
    - trigger AE_INITIAL_ACTION if answer YES to 'reportable_as_ae' or 'patient_admitted'

- Significant Diagnoses CRF:
    - add validation
    - trigger AE_INITIAL_ACTION if answer YES to 'gi_side_effects'
    - trigger AE_INITIAL_ACTION if answer YES to 'reportable_as_ae' or 'patient_admitted'

- ARV Treatment CRF:
    - add validation

- Patient Treatment CRF:
    - if Q4 'cm_confirmed' is YES
        - remove from study treatment
        - remain in follow-up
        - validate with study medication, to confirm taken off drug
    - if 'lp_completed', prompt for LP results

- Blood Result: FBC CRF:
    - Q3, 'requisition' + button doesn't work (no panels are listed)
    - ???validation

- Economics CRF:
    - everyone who has a medical event with any costs to them or trial to complete different CRF
        - then as PRN at subsequent follow-ups
    - Question: Has there been any events since last visit?

- Adherence CRF:
    - form validation (all)
        - consider adding "Are you speaking to patient?" lead question to validate against

- Adherence Diary
    - 14 days, 4 doses per day, reason for missed dose
    - user confirm number of missed doses (EDC to validate)
    - user confirm if there are 2 or more consecutive missed doses (EDC to validate)
    - if not filled in on D14 visit, EDC to prompts, until it is

- Missed Visit CRF:
    - awaiting

- Protocol violation/deviation CRF
    - awaiting

- End of Study/Termination CRF:
    - reconcile with provided form (08_Termination_Form_110821_V0.5.pdf)
    - add validation
    - check if started treatment, cannot be late exclusion

- Other (reported by JA):
    - Consent 2 and 3 – makes you add the name in full caps. Can this be made auto?
    - Requisition for blood sample gave server error – this prevents saving the bloods form.
    - I then added the requisition 992FC4G – thinking this was for a sample taken, but it seemed to only be for a FBC – and did not let me use it for chemistry results.
    - LP details – are these available?
