Amendments To The Cabinet Of Ministers Of 27 December 2005, Regulations No. 1037 "rules For Human Blood And Blood Components Collection, Testing, Processing, Storage And Distribution Of The Quality And Safety Standards"

Original Language Title: Grozījumi Ministru kabineta 2005.gada 27.decembra noteikumos Nr.1037 "Noteikumi par cilvēka asiņu un asins komponentu savākšanas, testēšanas, apstrādes, uzglabāšanas un izplatīšanas kvalitātes un drošības standartiem"

Read the untranslated law here: https://www.vestnesis.lv/ta/id/145512

Cabinet of Ministers Regulations No 841 Riga 2006 (October 10. No 52 30) amendments to the Cabinet of Ministers of 27 December 2005, regulations No 1035 "rules of human blood and blood components collection, testing, processing, storage and distribution of the quality and safety standards" Issued under the medical law of article 34 of the third to make a Cabinet of 27 December 2005, regulations No 1035 "rules of human blood and blood components collection, testing, processing, storage and distribution of the quality and safety standards" (Latvian journal , 2006, no. 8) the following amendments: 1. provisions supplementing the name after the words "security standards" with the words "compensation for expenses and lost blood volume restore." 2. Add to paragraph 1, after the word "raw" with the words "as well as compensation for expenses in the amount of blood lost restore." 3. Add to subparagraph 8.2.1., after the word "appreciable" by the word "State" of the blood establishment. 4. Replace paragraph 8.2.2., the words "blood preparation Department" with the words "the national blood center, blood Preparatory Department". 5. To replace the words "in paragraph 17.10. suspension of distribution" with the word "non-proliferation". 6. Supplement with 17.11. subparagraph by the following: "17.11. compensation for expenses in the amount of blood lost restoration amounting to: 17.11.1. blood donors — 3 lats; 17.11.2. rare blood groups (aloimunizēt-recipients) blood donors — 12 lats; 17.11.3. immune or donor aloimunizēt — 19 lats; 17.11.4. plazmoforēz procedure for the donor – 12 lats; 17.11.5. procedures for donor citoforēz — 20 lats; 17.11.6. blood donors who donate at the national blood Centre or blood preparations chapter call in an emergency, when lacks certain blood group of blood: 12 lats; 17.11.7. each donor a free meal for 1 dollar value. " 7. Supplement 24.2 point after the words ". to inform donors" with the words "in accordance with the donor's and the national blood Centre or blood preparation Department mutual agreement". 8. Make 41 as follows: "41. Information about human blood and blood components, traceability is kept for 30 years." 9. Supplement with 25.5 and 41.2 points as follows: "the national blood Centre 25.5 and blood preparations Department information about human blood and blood components, traceability include: 41.11. name and address of the institution; 41.12. the donor's name, surname, personal code, and the declared place of residence; 41.13. blood unit identification code; 41.14. individual blood component identification code; 41.15. blood preparation date (day, month, year); 41.16. news on blood and blood components distribution, medical institutions or their destruction. 41.2 the Office information on the blood human blood and blood components, traceability include: 41.21. supplier identification; 41.22. blood component identification code; 41.23. recipient's name, surname, personal code, and the declared place of residence; 41.24. pārlietaj units — not the approval of destruction; 41.25. transfusion or disposal date (day, month, year). " 10. Express annex 1 (1) of the following: 1. Determine ABO and Rh group affiliation. It is not determined for plasma intended only for fractionation. " 11. To supplement annex 1 to 2.4. subparagraph by the following: ' 2.4. antibodies to syphilis cause. " 12. the supplement to annex 3, paragraph 2, after the word "integrity" with the words "quality and". 13. Replace annex 5 paragraph, the word "2.2.9 carry" with the word "copy". 14. Replace 16.1 of annex 6, paragraph the word "served" with the words "distributed" and the word "izsniedzamaj" with the words "no izplatāmaj". 15. Express 6.16.2. subparagraph by the following: "the blood of 16.2, intermediate, and blood component labelling system organised in such a way to uniquely identify the blood, intermediate products, components and blood samples, as well as to comply with the labelling and traceability requirements." 16. Replace annex 6 in the 18.6, the word "integrity" not with the word "quality". 17. Make 7. in section 5.1.6.2. the following wording: "5.1.6.2. blood component identification code;".
Prime Minister a. Halloween Health Minister g. Smith