EUROLAB laboratory provides testing and compliance services within the scope of 9 CFR 113 28 standard. This standard specifies the requirements for cardiac infusion testing using supplied heart infusion water and heart infusion agar.
Immediately prior to testing, the frozen liquid vaccine should be thawed and the lyophilized vaccine rehydrated with mycoplasma medium to the volume recommended on the label. In the case of a lyophilized biological product, for example, a 1000-dose vial of poultry vaccine to be administered via drinking water, the vaccine should be rehydrated to 30 ml with mycoplasma medium. In the case of a cell line or primary cell sample, the inoculum will consist of resuspended cells.
Control tests will be run concurrently with the detection test using the techniques provided in paragraphs (d)(2) and (3) of this section, unless inoculum mycoplasma cultures and negative control testing are selected for the positive control test. will be uninoculated medium from the same lot used in the detection test.
EUROLAB assists manufacturers with 9 CFR 113 28 test compliance. Our test experts, with their professional working mission and principles, provide you, our manufacturers and suppliers, the best service and controlled testing process in our laboratories. Thanks to these services, businesses receive more effective, high-performance and quality testing services and provide safe, fast and uninterrupted service to their customers.
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EUROLABreporting and certification activities, United Accreditation Foundation (UAF), Turkish Accreditation Agency (TÜRKAK) ve Enterprise Accreditation Foundation (EAF) based on the accreditation provided by the accreditation body. The Enterprise Accreditation Foundation (EAF) accreditation body is also a signatory of the United Nations (UN GLOBAL COMPACT) organization.
