Pharmaceutical regulations emphasise on sterility being an integral part of quality control to adhere to pharmacopeial standards, ensuring that any product undergo stringent and vigorous sterility testing to assure its quality, efficacy and safety prior to its release. At MyGenome, sterility testing at our advanced laboratory facilities is conducted within a sterilised cleanroom environment in accordance with USP <71>, EP <2.6.1> and JP <4.06>.

Method Used: Membrane Filtration; Direct Inoculation