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Updated on:

June 3, 2026

This article has been updated to reflect the implementation of the EU PPWR, recent Canadian SUPPR regulatory shifts, and modern OECD testing criteria.

Biodegradation studies evaluate how microorganisms break down organic compounds into simpler substances under specific environmental conditions. These cont...


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Developing a new pharmaceutical compound is a highly complex, resource-intensive process. At the core of this journey—bridging the gap between initial discovery and clinical viability—are pharmacokinetics (PK) and pharmacodynamics (PD) studies. Together, PK/PD studies provide the essential data needed to understand how a drug interacts with the human body, ensuring both safet...


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Q. Please tell us about yourself. What brought you to your current position?

I’m a senior product manager at Thermo Fisher Scientific focused on molecular spectroscopy solutions, including FTIR and FT–Raman technologies. My background is in biophysics and analytical spectroscopy. Throughout my career, I’ve been passionate about helping scientists apply advanced analytical ...


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Key Takeaways Testing is a prerequisite, not an afterthought. Surplus laboratory assets require functional, calibration, and safety verification before redeployment or resale to protect downstream users and institutional liability. Regulatory requirements follow the asset, not the seller. Equipment subject to FDA, EPA, or NRC oversight re...

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Total Acid Number (TAN) and Total Base Number (TBN) testing are essential analytical methods used to evaluate the condition of lubricating oils, including engine oils, hydraulic oils, and industrial oils. These te...


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