News|Articles|August 19, 2026

Ensuring Sample Integrity from Discovery to Post-Market Surveillance

Author(s)Mesa Labs

An educational article examining how continuous environmental monitoring protects sample integrity across every phase of the drug development lifecycle, from discovery and preclinical research through clinical trials and post-market surveillance.


Related to this article

Pharma Logistician Using IoT Based On Blockchain | Image Credit: ©leowolfert -stock.adobe.com
Michael Levy, senior vice president, Digital & Innovation, USP, explains the digital supply chain in a preview of his upcoming CPHI Milan panel presentation, The Next Phase of Pharma Supply Chains.
AAPS PharmSci 360: CMC Strategies, Part 3
In a preview of their panel discussion at AAPS PharmSci 360 2026, Alfred Rumondor, PhD, AbbVie, and Swita Singh, PhD, Bristol Myers Squibb, discuss the implementation of risk-based approaches for CMC.