Trial period of the product has expired. The current trial product copy will be automatically blocked in 2 weeks. You can purchase the full version of the product on the site www.bitrix24.com. Department of quarantine of blood components and product Delivery
RSE on REM "Republican blood center" of the
Ministry of health of the Republic of Kazakhstan

Department of quarantine of blood components and product Delivery

Alimova Zukhra Mukhtarovna

Head of the Quarantine and Product Delivery Department


Has a higher medical education. In 1998 she graduated from the Kazakh State Medical University named after S.N. Asfendiyarov, "medical" faculty, specialty "General practitioner". In 1998, after graduating from the university, she was hired at the RSE at the Republican Blood Center as a doctor in the department of blood preparation and its components. From 2000 to 2006, she worked as the head of the department of drying and sterile bottling of blood products. From 2006 to 2008, she worked as the head of the organizational and methodological department. From 2009 to 2017, she worked as the head of the department of production of blood products. Since 2017 and up to the present time she has been the head of the department of quarantine and product delivery. He has the highest category in the specialty "Transfusiology".

She has completed the following advanced training courses:

  • «Topical issues of clinical and industrial transfusiology, including childhood» NCPT OF THE Ministry OF Health OF THE Republic of Kazakhstan
  • «Corporate governance in healthcare» CMU «VSHOZ»
  • Awarded with the diploma of the Minister of Health of the Republic of Kazakhstan for fruitful work in the field of healthcare.

Department of OK and VP consists of 2 blocks:

1) block for quarantine blood components

2) product dispensing block



The main tasks of the department:

  • 1) quarantine of fresh frozen and cryopreserved plasma;
  • 2) issuance of blood components and products in accordance with the requirements of quality standards, the terms of contracts and in compliance with the necessary requirements for storage and transportation.


OK and the VI does the following:

  • reception of fresh frozen plasma for quarantine storage and registration;
  • ensuring the storage regime of frozen plasma at a temperature not higher than -25˚С for 4 months and monitoring the storage regime;
  • summoning donors for repeated laboratory testing for transfusion infections;
  • destruction of plasma doses in case of primary positive laboratory test results for transfusion infections during quarantine or after the expiration of the quarantine period;
  • transfer of fresh frozen plasma for fractionation to the production of blood products;
  • delivery of fresh frozen plasma to medical organizations after the end of the quarantine period;
  • accepting and registering applications from MO;
  • placing orders in the Info Donor program;
  • receiving ready-made components and blood products from other structural units;
  • provision of temporary storage of components and blood products in compliance with temperature storage conditions and expiration dates;
  • on-line search of blood components in storage using the database of the Info-Donor information system for the timely and complete execution of MO orders;
  • issue of blood components and blood products in accordance with the Ministry of Defense's applications in accordance with the requirements of quality standards, the terms of contracts and in compliance with the necessary requirements for storage and transportation;
  • search for blood components in medical organizations (MO) using the data of the information system "Info Blood" in case of absence in the PCC and VP;
  • conducting a macro-assessment of incoming and outgoing blood components (preparations);
  • timely transfer of expired blood components for disposal with the registration of appropriate acts;
  • recall and destruction of blood components from donors diagnosed with vector-borne diseases;
  • maintaining accounting and reporting documentation on approved forms on paper and electronic media;
  • control over the implementation of the necessary measures to increase the responsibility of all links for the issuance of products that meet the established requirements and standards;
  • performing other functions within its competence in accordance with the goals and objectives of the enterprise.