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I have prepared a brief overview of the present situation
as you can see on this slide, we have a big problem for the inclusion of products in Form 4 and 8 products in GFR
Moreover, we plan to incorporate Benefiks, and consider the possibility to include Ksalkori and Inlayta in Orff list (where the Sutent and IRESSA (gefitinib))
This slide shows a detailed plan for inclusion in the lists for Ksalkori and Inlayta, execution date until the third quarter of this year,
I want to focus on the challenges that we are facing or will face in the future, which does not depend on us
1 ) Most of the territory of Kazakhstan, 16 regions, before you sign a letter of justification, need some time to meet with experts, after the signing of letters main external experts, the next step is to sign the letters from the regional health departments to make the Ministry of Health
2) Formulary Committee meetings are not regular There are no regulatory approval.
Meetings may be held once a quarter or twice a month
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