Results (
English) 2:
[Copy]Copied!
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))
The process of inclusion of 8 products runs parallel with the same deadlines
This slide shows a detailed plan for inclusion in the list for six Ksalkori and Inlayta, execution date until the third quarter of this year
are listed here to provide the required documents, the date and status
I want to focus on the challenges that we are facing or will face in the future, which does not depend on us
1) A large area of Kazakhstan, 16 regions, before you sign a letter of justification, need some time to meet with experts, after the signing of letters of the 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 is no regulatory approval.
Meetings are held once a quarter or twice a month
on this slide shows the current situation
you can see, for GFR we signed five letters and one file for GFR, now you need to sign three letters for GFR period - April 3
Being translated, please wait..
