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The EPA's PFAS public hearing has concluded, but the written comment period remains open until July 20. For chemical procurement professionals, well-supported written submissions can have a greater influence on the rulemaking record than hearing testimony alone.

TSCA Week Two: How Chemical Companies Are Managing the Post-Fee-Expiry Transition
Two weeks after TSCA's fee authority expired, chemical companies are adapting to longer PMN review timelines and changing compliance priorities. Learn how to prepare your regulatory strategy.

Modified Starch and the EU's OSOA Platform: First Week of the New Compliance Architecture
The EU’s new One Substance-One Assessment framework officially launched July 1, reshaping compliance workflows for food ingredient buyers supplying into Europe. Companies sourcing modified starches and food additives must now adapt to ECHA’s centralized regulatory architecture and updated compliance processes.

Indian Medical Device Polymer Inputs: Day Two Without Duty Waiver and What It Means for Procurement
India's medical device manufacturers have entered a new cost environment following the reinstatement of customs duty on key polymer inputs. Procurement teams should prepare for higher supplier quotations as the industry seeks government relief.

TSCA Post-Expiry: H1 Closing Status and the August Recess Risk
The expiration of TSCA fee authority has introduced new regulatory uncertainty for pharmaceutical and specialty chemical manufacturers. Companies with pending EPA submissions should closely monitor legislative developments throughout H2 2026.

TSCA 2026: Immediate Actions After Fee Authority Expiry
When the TSCA fee authority expires in 2026, chemical manufacturers, importers and compliance teams face a new set of obligations. This article outlines the urgent steps required to stay compliant, from PMN filing updates to EPA chemical review adjustments. Read on to ensure your operations remain uninterrupted.
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