| From : | Mirela Busic <mirela.busic@gmail.com> |
| To : | Natia Nogaideli <natianogaideli@yahoo.com> |
| Subject : | Re: RIA Reports (ORGANS, TISSUES and CELLS) |
| Cc : | Achi Zangurashvili <a.zangurashvili@gmail.com>; Vakhtang Chkheidze <v.chkheidze1957@gmail.com>; vanja.nikolacm@gmail.com; Tamar Gabunia <tgabunia@moh.gov.ge>; Anzor tchavtchavadze <atchavtchavadze@moh.gov.ge>; Laura Carrasco Macia <laura.carrasco@dt-global.com>; KOCHISHVILI Nika (EEAS-TBILISI) <nino.kochishvili@eeas.europa.eu> |
| Received On : | 02.04.2021 11:19 |
Dear Mirela,I hope you are doing well.Unfortunately, the law sent in February is quite different from the version prepared in August 2020. Consequently, the law needed to be re-drafted. Although, I had written to you on 4-th March about our disagreement over certain articles, in the version, sent by you on 6th of March, our opinions haven’t been taken into account.
We believe, the draft law presented in the Ministry should be in full compliance with Euro Directives. Moreover, during the preparation of the draft law Georgian Legislation, the structure of the healthcare system, functions, and responsibilities of the Ministry of Health, redistribution of responsibilities between state agencies, funding system for medical services, social, cultural, and economic characteristics of the country should be taken into account.
In the attached file you can find a corrected version of the draft law with our opinions in track-change format. I want to clarify some issues, which I did not agree with and have corrected in the text:
a) Some definitions, that have no need to be in the law, have been taken out. For example All institutions that will become a ‘Procurement Center’ - nowadays has permission, there will be no new permit/license for the Procurement Center, beside some additional requirements must be met within the existing permits; As for ICU Departments - ICU departments in all multi-profile clinics will have an obligation to participate in determining the death of a potential donor and in all appropriate procedures (Which will be regulated by amending the existing permit requirements); Also, Death, Death declaration, Brain death, ........ have been removed from the definitions, according to the Georgian normative technique the National diagnostic protocol for determination of death cannot be a part of the law;
b) At this point live donation is a well-regulated area in Georgia. While kinship donation and cross-donation, the transplantation is approved by the Transplantation Council, and for emotional connection - the court approval is needed. Cross-donation does not involve the exchange of organs during an emotional connection. Consequently, the existing system of live donation should remain, as long as it is based on altruistic donation and the risks are minimized;
c) National Protocol for Determination of Death has been removed from the law, because according to the legislation of Georgia, as well as the established practice, such issues cannot be regulated by the law; At the same time, the issues of national protocols’ recognition are regulated by the Law of Georgia on Health Care; The protocol will be approved after discussion with the medical associations according to the current legislation;
d) Issues for granting the right to operate are regulated by the Law of Georgia on Licenses and Permits; Permit and license is permanent; That is the reason why we are introducing the concept of a certificate, which needs to be updated every 4 years. It gives the opportunity to inspect transplant centers once every 4 years. Procurement Centers will be all multi-profile hospitals that operate within the permit. Amendments will be made in permit conditions to ensure procurement of organs in these clinics. Legislation in Georgia does not provide for the suspension of a permit/license.
I think the naming of chapters and articles should be revised with Archil.
Some issues need to be discussed with the ministry, primarily the establishment of the National Center for Substances of Human Origin.
It is important to review the final agreed version of the law during March 22-27. Open issues will be discussed with the ministry in later periods.
I sent you a revised version of the Tissues Law on March 4th (I do not agree with certain articles in the bill you submitted). Timely completion of the Tissue Law is also very important. Maybe we will go through this law together on March 28-29.
Looking forward to your feedback.Kind regards,NatiaOn Wednesday, March 17, 2021, 07:26:06 PM GMT+4, Mirela Busic <mirela.busic@gmail.com> wrote:Thank you, confirmed.sri, 17. ožu 2021. 12:39 Vakhtang Chkheidze <v.chkheidze1957@gmail.com> je napisao:Dear Mirela,Thank you for your email.I am also available tomorrow at 4 PM your time (7 PM my time).Talk to you tomorrow.Kind regards.VakhtangOn Wed, 17 Mar 2021, 14:26 Mirela Busic, <mirela.busic@gmail.com> wrote:Dear Vakhtang,happy to do that, I'm available tomorrow at 4 pm my time, 7 pm your time, if convenient for you?MirelaOn Wed, Mar 17, 2021 at 10:07 AM Vakhtang Chkheidze <v.chkheidze1957@gmail.com> wrote:Dear Mirela,Thank you for sending the draft versions of the RIA documents.I would like to have an online meeting with you concerning these new documents - just briefly to have a discussion about this matter.Please inform me - when we can have an online meeting at any convenience for you time? By Zoom or Whatsapp.Looking forward to hearing from you.Thank you in advance.Kind regards.VakhtangOn Tue, Mar 16, 2021 at 5:01 PM Mirela Busic <mirela.busic@gmail.com> wrote:Dear colleagues,in continuation to our online meetings held to agree on the last version of the laws, please find the draft versions of the RIA documents accompanying the law proposals.In this stage of finalisations of the Law proposals and RIAs, I suggest a meeting with the beneficiary ( Mrs Tamar, and Mr Anzor) for consultation on the next steps that entails;- public consultations (we should agree on date for the launch of public consultation and its operative management)- organisation and date of the online one-day workshops to present and discuss the proposed policy with all stakeholdersMeanwhile, I would appreciate your inputs for improvements and completion of the RIA documents (written in a separate documents).Thank you for your, so far, contribution in the process of finalisation of the new law proposals and initial input for the RIA (Tissues and cells) kindly provided by Vakhtang.Looking forward to your feedbackMirela--