Anforderungen an das HCT/P-Umgebungsmonitoring
The Food and Drug Administration (FDA) requires human cell, tissue, and cellular and tissue-based product establishments to follow the current Good Tissue Practice (GTP). An introduction of the regulation and a recommendation of frequency of monitoring for particles and microbial agents is provided.
Interested in learning more? Complete the form on this page to receive a free copy of the HCT/P Environmental Monitoring Requirements application note.