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PFAS in Medical Devices: How Compliance Software Helps Identify and Manage Risk
The risk of PFAS in medical devices continues to burden MedTech compliance teams as global...
4 minute read
TSCA Section 8(a)(7): A Guide to the PFAS Reporting Rule Under TSCA
The United States (U.S.) Environmental Protection Agency (EPA) has recently finalized a new per-...
3 minute read
Frequently Asked Questions About the EPA’s PFAS Reporting Rule Under TSCA
There are many questions about the PFAS reporting rule under TSCA Section 8(a)(7), which requires...
7 minute read
ESG Compliance Software: Turn Complex Requirements Into Actionable Data
ESG compliance software is becoming essential as ESG moves from a reporting exercise to a...
4 minute read
Understanding the EU Ecodesign for Sustainable Products Regulation (2024/1781) and the Digital Product Passport
The EU Ecodesign for Sustainable Products Regulation (2024/1781) is reshaping access to the...
4 minute read
Medical Device Compliance Standards: Key Risks and Requirements
Medical device manufacturers face a complex compliance environment that is broader, faster, and...
5 minute read
EU RoHS Compliance in 2026: What to Expect
EU RoHS compliance in 2026 will be shaped less by new substance restrictions and more by tightening...
5 minute read
What is an SVHC under EU REACH?
SVHCs—or Substances of Very High Concern—are chemicals identified by the European Chemicals Agency...
4 minute read
New Global PFAS Regulations: How to Remain Compliant in 2026
Global PFAS regulations are accelerating worldwide as governments respond to growing evidence of...
12 minute read
