Consultancy for IoT Compliance & Certification
We provide expert IoT compliance consultancy services for manufacturers, integrators, and importers. Our team helps you navigate CE marking, FCC approvals, RED Directive Article 3.1a, 3.1b, 3.2, 3.3 (d/e/f), EMC, Radio, and IoT cybersecurity compliance to achieve faster and smoother market access.
Why Consultancy Matters
Global IoT regulations are evolving rapidly. Manufacturers face overlapping requirements across CE (Europe), FCC (USA), UKCA (UK), MIC (Japan), ISED (Canada), SRRC (China) and the rest of the world, as well as new cybersecurity obligations under EN 18031 and the EU Delegated Act 2022/30.
Without expert guidance, compliance can lead to delays, redesigns, or rejected certifications — blocking market entry. Our consultancy ensures you understand requirements from the earliest design phase, reducing risk and accelerating time-to-market.
Our Consultancy Services
- Compliance Strategy & Planning -Identify relevant directives and standards (RED, EMC, Safety, Cybersecurity) and create a roadmap for global approvals;
- Gap Analysis & Risk Assessment - Review your product design against requirements to prevent costly redesigns and ensure regulatory readiness;
- Testing Roadmaps & Lab Coordination - Plan EMC, Radio, Safety, and Cybersecurity testing. We leverage our partnerships with accredited labs worldwide to streamline the process;
- Technical Documentation & Files - Support with Technical Construction Files (TCFs), Declarations of Conformity (DoCs), (STRIDE) risk analyses, and RED Article 3.1a, 3.1b, 3.2 and 3.3 compliance;
- Global Market Access Consultancy - Guidance for countries worldwide — one partner for worldwide approvals;
- Cybersecurity & Industry-Specific Support - Tailored consultancy for IoT cybersecurity (EN 18031, EU 2022/30) and industry-specific requirements: MDR 2017/745 (medical devices), Industry 4.0 IoT systems.
Your Trusted Compliance Partner
At IoT Consulting Partners, consultancy is more than advice. It’s a hands-on path to certification. From IoT radio; EMC and cybersecurity consultancy to global market access planning, our team ensures your product is compliant, secure, and ready for worldwide deployment.
Explore Our Expert Consultancy Insights in the Articles Section
| Article Title | Summary | Key Topic |
|---|---|---|
| Understanding the Key Differences Between RoHS and REACH: A Comprehensive Guide | Explains how RoHS restricts hazardous substances in electronics, while REACH governs the broader chemical use across industries—clarifying compliance scopes and challenges. | RoHS vs. REACH: Environmental Compliance |
| Do I Need an Authorised Representative? | Clarifies when appointing an EU or UK Authorized Representative is mandatory—especially since Regulation 2019/1020 came into force in July 2021—and highlights their essential role in market surveillance. | Role of Authorized Representatives (EU/UK) |
| Avoid Market Surveillance Pitfalls: Ensure EU Product Compliance | Offers best practices to stay inspection-ready—covering documentation, cooperation with authorities, and readiness for incoming rules under the Product Liability Directive. | EU Market Surveillance & Product Liability |
| CE Certification and the CE Mark | Provides a practical overview of harmonized standards, essential requirements, and Declaration of Conformity (DoC) creation for CE marking under RED. | CE Marking Fundamentals (Radio Equipment) |
| IoT Consulting Partners 2014/53/EU Compliance Test Plan | Explains how to structure your test plan for RED (2014/53/EU) compliance—from testing scope to required deliverables and Notified Body interactions. | RED Compliance: Test Planning |
| Key Elements of Technical Documentation Under Directive 2014/53/EU (Annex V) | Breaks down RED Annex V documentation – including diagrams, harmonized standards list, test reports, Declaration of Conformity, and NB involvement. | RED Annex V: Technical File Essentials |
| Risk Assessment for IoT Compliance: Insights from REDCA TGN 30 | Guides manufacturers through REDCA TGN 30 risk assessment steps—highlighting when to adopt Notified Body exam and how to document risk mitigation effectively. | RED Risk Assessment & Notified Body |
| Download Your Free EU Declaration of Conformity Template for Directive 2014/53/EU | Provides a downloadable DoC template aligned with RED Annex VI and explains how to complete and implement it for legal market access. | RED DoC Template (Annex VI) |