We are committed to ensuring safe access to high-quality FMT and ensuring that we are compliant with regulatory requirements. To this end, we require that all clinical partners that utilize our FMT products report all adverse effects (AEs) / Adverse Drug Reactions to Novel Biome within 24 hours and, if required, their regulatory health body.
Please note, if you are reporting a severe AE, someone from our team will reach out to you to collect more detailed information.