Fast track registration – until 2022
Fast track registration – Order of Russian Government 430 (as well as 804) – is prolongated until 2022. Already issued registration certificates should be renewed.
Read moreCategory Archives: IVD regulation
Toxicology tests for in vitro diagnostics
Toxicology tests for medical devices intended for in vitro diagnostics are to be performed in order to determine any possible harmful effect of a material or device on the human body, caused by a toxicity factor. These tests have to be performed for medical devices intended for immediate contact with the human body, when used as per the intended indications
Read moreImmunochemiluminescent analysis as a diagnostic method
Currently, there are many models of automatic analyzers that differ in the method used to detect the desired substance. The main analysis methods used are: – radioimmunological (RIA); – enzyme-linked immunosorbent assay (ELISA); – Immunofluorescence; – immunochemiluminescent; – immunochromatographic; – isoserological. Let us consider in more detail immunochemiluminescent analysis. Immunochemiluminescent analysis is based on the enzyme immunoassay. The principle of
Read moreTechnical testing of medical devices for in vitro diagnostics
According to the Government of the Russian Federation decree dated 27 December 2012 No. 1416 “On the approval of the rules state registration of medical devices” the term “technical testing” is defined as the testing to determine whether the characteristics (properties) of the medical device meet the requirements of the regulatory, technical and operational documentation of the producer (manufacturer) and
Read moreRegistration procedure for medical devices for in vitro diagnostics
A medical device for in vitro diagnostics is any medical device intended by the manufacturer to study samples of human biological material without contact with a patient in separate application or in combination with other medical devices, only for the purpose of obtaining regarding physiological or pathological condition, and (or) fetal development problems, and (or) monitoring therapeutic interventions, and (or)
Read moreUrgent registration process for Covid-19 tests is approved by Government
Order of Russian Government 430 from 03th of April 2020 was published yesterday (06th of April 2020), what is inside: list of products intended to be used in special conditions (emergency, martial law and so on). In this list – IVD test for COVID-19, thermometers, artificial ventilator apparatus; registration certificate is issued on the base on series/LOTs of medical
Read moreTHE IMPACT OF POTENTIALLY INTERFERING SUBSTANCES ON THE RESULTS OF CLINICAL LABORATORY TESTS
The reliability and accuracy of the sample results in clinical laboratory tests are influenced by many factors, such as the preanalytical factor, sampling, transportation, storage of samples, as well as the presence of interfering substances in the biomaterial samples. Interfering substances are one of the most common errors in clinical laboratory measurements. The presence of these substances in the samples
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