MEDIA FILL PK Kit enables aseptic process validation in terms of operator skills and of the manual procedures adopted through sterile radiopharmaceutical preparation targeting the operator abilities and working procedures.according to Chapter 11 of “Good Preparation Procedures in Nuclear Medicine”.
Media-Fill procedure is closely linked to the operating procedures of each individual department and cannot be generalised. The leaflet suggests a possible operational sequence, that must be approved by the responsible personnel of the Nuclear Medicine Department.
Incubation/reading/fertility service and drafting of analysis reports
At the end of the three simulations, all of the samples collected may be shipped to Eurofins for incubation at the temperature of 22.5°C/32.5°C for a total of 14 days. The sterile samples then undergo a fertility test performed to verify the compliance of the culture medium.
Upon completion of the tests, the quality control department issues an analysis certificate containing the results of the analytical tests performed on the samples.
Validation protocol and final report
1MP, on request, will provide technical support for the definition and revision of the validation protocol and respective report. The latter constitutes indispensable documentation for demonstrating the performed work compliance to applicable standards.
