Thank you for your interest in the white paper: Implementing Successful Mapping Solutions.
All organizations or individuals involved in the storage or distribution of drug products for human or veterinary use must practice good storage and distribution practices per Food and Drug Administration (FDA) requirements. It is integral and critical for pharmaceutical, biologics, cell and gene therapies, and medical device companies to map, validate, and continuously monitor ambient environmental conditions for all storage and distribution practices from the storage of raw material to the finished end product.
Find out what Testo offers when it comes to ensuring your environmental conditions are mapped within GMP compliance.
