QUALITY ASSURANCE AND QUALITY CONTROL OF RADIOPHARMACEUTICALS: AN OVERVIEW
Abstract
Result and Discussion: Radiopharmaceuticals should be prepared in accordance with standards specified in relevant sections of pharmacopoeias. For each series of radiopharmaceuticals, tests prescribed in the pharmacopoeias and records must be kept. Production and preparation of radiopharmaceuticals should be carried out in accordance with Good Manufacturing Practices for sterile preparations and GRP for radioactive products. However, radiopharmaceuticals that pass quality control tests can be administered to patients after dose measurements are made in dose calibrators. Thus, the patient's safety and benefit are maximized, while the risk is minimized. Some radiopharmaceuticals with a short half-life are used before quality control tests are completed. In this case, the effectiveness and continuation of the quality assurance system should be tested at appropriate intervals. According to procedures performed by hospital radiopharmacy laboratories, international standards are determined as Level IA/B, Level IIA/B and Level IIIA/B/C. Quality assurance of radiopharmaceuticals is provided by a sufficient number of trained personnel within the scope of GRP, devices that have been calibrated and controlled, appropriate substances and a working order in which tests determined at each stage are made and results are recorded accurately and regularly.
Keywords
References
- Ekinci, M., İlem-Özdemir, D. (2021). Radyofarmasötikler ve teranostikler. Journal of Literature Pharmacy Sciences, 10(1), 119-132. [CrossRef]
- 2. Wadsak, W., Mitterhauser, M. (2010). Basics and principles of radiopharmaceuticals for PET/CT. European Journal of Radiology, 73(3), 461-469. [CrossRef]
- 3. Shukla, J., Vatsa, R., Garg, N., Bhusari, P., Watts, A., Mittal, B.R. (2013). Quality control of positron emission tomography radiopharmaceuticals: An institutional experience. Indian Journal of Nuclear Medicine, 28(4), 200-206. [CrossRef]
- 4. Guideline on Radiopharmaceuticals, CHMP, EMEA/CHMP/QWP/306970/2007 (draft released for consultation) Web site. (2007). From http://www.emea.europa.eu/pdfs/human/qwp/ 30697007en.pdf. Accessed: 17.01.2022
- 5. European Pharmacopoeia. (2009). Radiopharmaceutical Preparations, Online 8.5.
- 6. Saha, G.B. (2018). Nuclear Pharmacy. In: Fundamentals of Nuclear Pharmacy, 3rd ed, (pp. 185-202).
- 7. Bringhammar, T., Zolle, I. (2007). Quality Assurance of Radiopharmaceuticals. In: Zolle, I. (Ed.), Technetium-99m Pharmaceuticals: Preparation and Quality Control in Nuclear Medicine, (pp. 67-75). Springer-Verlag Berlin Heidelberg.
- 8. International Atomic Energy Agency Web site (2018). Quality control in the production of radiopharmaceuticals. From https://www-pub.iaea.org/MTCD/Publications/PDF/TE-1856web.pdf Accessed: 17.01.2021
Details
Primary Language
English
Subjects
Pharmacology and Pharmaceutical Sciences
Journal Section
Review
Authors
Meliha Ekinci
0000-0003-1319-3756
Türkiye
Publication Date
September 30, 2022
Submission Date
April 27, 2022
Acceptance Date
July 1, 2022
Published in Issue
Year 2022 Volume: 46 Number: 3
Cited By
Quality Assurance and Quality Control Methods in Radiopharmacy
Nuclear Medicine Seminars
https://doi.org/10.4274/nts.galenos.2023.0010