cGMP (FDA 21 CFR Part 820): Current Good Manufacturing Practice for Medical Devices. Pertains to the manufacturing and packaging of human and animal cell culture media. ISO (9001:2008): Applies to the manufacture and supply of human and animal cells and related products for research use.
**Important Note: This information has been provided by the Company and has not been confirmed by Contract Laboratory Inc. It is recommended that you confirm all information prior to using this company.