ABSTRACT
Appropriate quality control measures are mandatory to ensure the efficacy and safety of the used media.
Testing IVF media involves sterility, endotoxin levels, pH, osmolality, and visual inspection. It ensures that the media are safe and effective for IVF procedures, ultimately enhancing the chances of successful implantation and pregnancy.
The purpose of conducting these tests is to verify the absence of any potential contaminants, confirm all required chemical properties, and establish the safety of the media for use in ART procedures.
Maintaining the integrity of IVF media requires adherence to appropriate storage conditions.
Regular monitoring of storage conditions is required to ensure the viability of the media.
IVF media is a complex mixture of nutrients and other substances essential for embryo growth and development. Once opened, the media begins to degrade, and its effectiveness declines over time. Therefore, it is vital to use IVF media within the recommended timeframe and to discard any unused media.
The recommended timeframe for IVF media varies depending on the specific media and the manufacturer’s instructions.
QC testing for IVF media must be well documented to provide responsibility and traceability.
Records of quality control tests must contain the date, test results, and the name of the technician who carried out the test.
This document thoroughly outlines the media’s composition, providing specifics on the concentrations of all components, the pH value, osmolality, and ionic strength.
Adhering to stringent quality control standards for IVF media and disposable materials is crucial to ensure a reliable and secure setting for assisted reproduction. Compliance with these standards ensures they meet requirements and specifications, thus mitigating potential risks and maximising the success of the procedures.
