Source Intelligence Blog

ESG Compliance Software: Simplify ESG Reporting and Manage Data at Scale

info@sourceintelligence.com (Source Intelligence) — Thu, 02 Apr 2026 20:30:00 GMT

ESG compliance software is becoming essential as ESG moves from a reporting exercise to a business-critical requirement. Companies are now expected to track, validate, and disclose environmental and social data across their operations and supply chains. But the challenge isn’t awareness—it’s execution.

Safer Chemistry in Product Design: How Google Scales Chemical Risk Management

info@sourceintelligence.com (Source Intelligence) — Tue, 31 Mar 2026 12:48:39 GMT

How hazard data and workflow integration enable proactive, safer material decisions at scale

Supply Chain Compliance News: Regulatory Updates and ESG Reporting Standards

info@sourceintelligence.com (Source Intelligence) — Fri, 27 Mar 2026 18:00:00 GMT

Track the latest supply chain compliance news, regulatory updates, and changes to ESG reporting standards

Understanding the EU Ecodesign for Sustainable Products Regulation (2024/1781) and the Digital Product Passport

Tiahna Broderick — Mon, 23 Mar 2026 17:00:00 GMT

The EU Ecodesign for Sustainable Products Regulation (2024/1781) is reshaping access to the European Union market by requiring companies to demonstrate product sustainability with more complete, verifiable data. Regulators are moving beyond isolated product attributes and toward full lifecycle transparency, with new expectations for durability, repairability, recyclability, and environmental performance across nearly all physical goods.

Source Intelligence Earns SOC 2 Type II Report for SaaS Security

info@sourceintelligence.com (Source Intelligence) — Mon, 16 Mar 2026 18:00:00 GMT

Achievement validates commitment to data security and trusted SaaS operations

Medical Device Regulatory Compliance Guide: PFAS, Supplier Data & Enforcement Risk

Anne Barr — Fri, 06 Mar 2026 16:00:00 GMT

A practical MedTech compliance guide to PFAS, materials of concern, and audit exposure

Medical Device Regulatory Compliance: Standards, Supplier Risk, and Data Requirements

Anne Barr — Tue, 03 Mar 2026 14:00:02 GMT

Medical device manufacturers face a complex compliance environment that is broader, faster, and more demanding than ever before. The challenge is no longer simply understanding regulations. Manufacturers must be able to quickly and defensibly prove compliance across materials, sourcing, and suppliers.

2026 Medical Device Compliance Guide: MDR, Chemicals, PFAS, and EPR

info@sourceintelligence.com (Source Intelligence) — Thu, 26 Feb 2026 22:30:57 GMT

How medical device teams can prepare for 2026 regulatory change across procurement, risk, and compliance

REACH Compliance in 2026: Updates and Supply Chain Compliance Solutions

Clement West — Thu, 26 Feb 2026 17:00:00 GMT

EU REACH compliance in 2026 requires more than tracking updates. The European Union (EU) is tightening chemical controls under the Registration, Evaluation, and Authorization of Chemicals (REACH) framework, and having reliable supplier data and automated compliance processes is necessary to reduce risk. For compliance teams, 2026 is a transition year. New documentation, labeling, and risk management obligations begin before the first PFAS prohibition in firefighting foams takes effect in 2030. This blog explains what is changing, who is affected, and which EU PFAS deadlines to prioritize.

EU RoHS Compliance in 2026

Clement West — Tue, 17 Feb 2026 20:30:00 GMT

EU RoHS compliance in 2026 will be shaped less by new substance restrictions and more by tightening EU RoHS lead exemptions, revised lead thresholds, and approaching renewal and expiration deadlines. While the restricted substances list remains unchanged, manufacturers must prepare for delegated directive updates taking effect in 2026 that will significantly impact how exemptions are managed across products and materials.

Businesses subject to the EU Restriction of Hazardous Substances Directive (EU RoHS) must stay focused on exemption tracking, supplier data accuracy, and defensible documentation to maintain compliance as new requirements are transposed and implemented across Member States.