Report patients treated and funds drawn under the national rare-diseases policy, for a designated centre.
Offered in: India only.For a hospital designated a Centre of Excellence under the National Policy for Rare Diseases (MoHFW, 2021). Each patient approved for support is recorded with the disorder as diagnosed, the policy group the approving committee placed it in, the approval’s date and reference, and the amount approved for that patient with where it comes from — the policy’s ceiling changes by notification, so none ships. One open approval per patient, closed with a reason when it ends. Every draw of funds names the day, the amount, what it was for — a drug, a procedure, an investigation or something else in words — and the bill it pays, and the draws for a patient can never pass the amount approved: the desk refuses it, and so do the rows themselves. Each patient shows what has been drawn and what is left. Each month the report is counted — patients with an open approval, new approvals by group, patients treated, funds drawn (drugs among them), drawn to date and approvals fully drawn — filed by hand and its acknowledgement recorded.
/rare-disease-coerarecoe.readWhat it does not do, by design. A listing with only benefits is an advertisement.
Read out of the code, not the brochure: each app below is here because one service queries the other’s tables. Install either side and the hand-over is already wired.
Tell us what you run and we will show you this app inside a practice shaped like yours — or answer the question the page above did not.