Agent Registry·Intelligence·Regulatory Intel Agent

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Regulatory Intel Agent

Monitors Federal Register, SEC, CISA, and global regulators for rule changes that affect your program.

Daily scan of regulatory sources — Federal Register final and proposed rules, SEC cybersecurity disclosures, CISA guidance, EU DORA/NIS2 updates, India DPDPA rulemaking. Summarizes what changed, who is affected, and what action is required by what deadline.

Tools:web_searchweb_fetch

Frameworks:FedRAMPCMMCDPDPANIS2DORASECHIPAA

Use case 1

You need a daily regulatory intelligence brief but cannot read the Federal Register every morning

→ 5 to 10 entry brief filtered to your jurisdiction and sector, with deadlines and the specific actions required

Use case 2

Compliance officer asks 'what is coming up next quarter?'

→ 90-day forward-looking calendar of effective dates across SEC, FTC, EU regulators, RBI, OPC with owner assignments

Use case 3

Counsel needs background on a new rule before drafting client advice or board memo

→ Rule summary with effective date, scope, key requirements, current enforcement signals, and authoritative source links

Try a sample prompt:

regulatory-intel-agent · live demo · gemini-flash

◇ Curated sample output (real format)

Regulatory Intel Brief · 2026-05-09 · Healthcare SaaS

EU AI Act · Article 6 (High-Risk AI Systems) · Enforcement starts 2026-08-02

Issuing body: European Commission

Affects: Any AI system deployed in EU classified as high-risk under Annex III (includes AI used in healthcare diagnostics, credit scoring, hiring, law enforcement)

What changed this week: The EU AI Office published the final implementing regulation for Article 6 conformity assessment procedures on 2026-05-07. It clarifies that providers may use harmonised standards (forthcoming) OR demonstrate equivalent conformity. ISO/IEC 42001:2023 is named as one acceptable basis.

If you are deploying clinical-decision AI in the EU:

1. Determine if any of your AI systems fall under Annex III §5 (healthcare device) — affirmative for any diagnostic/triage AI

2. Begin ISO 42001 readiness if not already (provides Article 6 conformity basis)

3. Designate an EU representative if you have no EU establishment

4. Prepare technical documentation per Annex IV

Priority: Immediate (90 days to enforcement)

Source: https://artificialintelligenceact.eu/article/6/

SEC Cyber Disclosure · 8-K Item 1.05 · Materiality clarification

Issuing body: SEC Division of Corporation Finance

Affects: US public companies (and via supply chain pressure, their vendors)

What changed this week: Two new comment letters published on EDGAR (April 28, May 2) reject corporate filings that used "operational impact pending assessment" as a deferral. The Division reasserts that materiality is a four-day clock from materiality determination, not from operational stability.

If you are SEC-reportable:

1. Pre-trigger your "materiality determination" playbook with Legal — practical rule: any incident affecting >2% of customers OR triggering credit-rating implications requires same-day materiality memo

2. Have draft 8-K Item 1.05 template ready, not started during incident

Priority: This quarter

Source: SEC EDGAR comment letters CL-2026-04-28-PRGS, CL-2026-05-02-WTHR

India DPDPA 2023 · Rules Draft Released

Issuing body: Ministry of Electronics and IT (MeitY)

Affects: Any entity processing personal data of individuals in India

What changed this week: Draft rules published 2026-05-05 for 45-day public comment. Key items:

1. Significant Data Fiduciary (SDF) threshold proposed at 10M data principals

2. Cross-border transfer mechanism: allowlist of countries to be notified

3. Children's data: explicit consent + age 18 threshold

4. Breach notification: 72 hours to Data Protection Board AND data principals

If you process India user data:

1. Estimate your Indian data principal count — are you near SDF threshold?

2. Map your subprocessors and transfer mechanisms (US-based AWS region transfer is currently unrestricted; this may change)

3. Comment by 2026-06-20 deadline if rules affect you

Priority: This quarter (final rules expected Q3 2026)

Source: https://www.meity.gov.in/data-protection-framework

What I am not flagging this brief

- FedRAMP 20x SSP automation pilot update — not yet relevant to Acme tier

- DORA further guidance — Acme not regulated under DORA

- 14 other items reviewed and filtered as routine or out-of-scope

Forward calendar (next 30 days)

Date	Event	Action
2026-05-20	EU AI Act conformity assessment guidance	Read, brief CTO
2026-06-01	OCR HIPAA Security Rule NPRM expected	Watch for our SRA scope expansion
2026-06-20	India DPDPA rules comment deadline	Submit comment if needed

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