CE Marking
EU marking for product conformity to harmonised legislation
TOGAF
Vendor-neutral framework for enterprise architecture methodology
Quick Verdict
CE Marking mandates EEA product safety compliance via self-declaration or notified bodies, enabling market access. TOGAF is a voluntary framework for enterprise architecture, aligning business/IT strategy. Manufacturers require CE for legal sales; enterprises adopt TOGAF for transformation efficiency.
CE Marking
CE Marking (Conformité Européenne)
Key Features
- Manufacturer self-declares conformity to EU essential requirements
- Enables free circulation across EEA single market
- OJEU harmonized standards provide presumption of conformity
- Risk-proportionate conformity assessment modules A-H
- Requires 10-year technical file retention obligation
TOGAF
TOGAF Standard, 10th Edition
Key Features
- Iterative Architecture Development Method (ADM) lifecycle
- Content Framework with metamodel for artifacts
- Enterprise Continuum for reusable architecture assets
- Reference models like TRM and III-RM
- Architecture Capability Framework for governance
Detailed Analysis
A comprehensive look at the specific requirements, scope, and impact of each standard.
CE Marking Details
What It Is
CE Marking (Conformité Européenne) is the EU's core product compliance marking under the New Legislative Framework (NLF). It's a manufacturer's declaration that products meet essential requirements in harmonised legislation (e.g., LVD 2014/35/EU, Machinery Directive). Scope covers health, safety, environmental protection for categories like electronics, machinery, toys. Key approach: risk-based conformity assessment via modules A-H, using OJEU-published harmonised standards for presumption of conformity.
Key Components
- Legislation mapping and essential requirements identification
- Conformity assessment (self-declaration or Notified Body involvement)
- Comprehensive technical documentation (design, tests, risks)
- EU Declaration of Conformity (DoC) issuance
- Precise CE mark affixing rules
- Post-market surveillance obligations Built on NLF principles; no fixed control count, certification via self/3rd-party.
Why Organizations Use It
Mandated for EEA market access; mitigates legal risks (fines, recalls); enables free movement across 30+ countries. Builds stakeholder trust, competitive edge via compliance excellence, reduces liability.
Implementation Overview
Map directives, perform risk assessment/testing, compile technical file/DoC, affix mark. Applies to manufacturers/importers selling regulated products in EEA; involves audits for high-risk. Typical: cross-functional teams, 6-12 months low-risk, longer with Notified Bodies.
TOGAF Details
What It Is
TOGAF® Standard (The Open Group Architecture Framework) is a vendor-neutral enterprise architecture framework. Its primary purpose is to provide a proven methodology for designing, planning, implementing, and governing enterprise-wide change across business and IT. The core approach is the iterative Architecture Development Method (ADM).
Key Components
- **ADM phasesPreliminary, Vision, Business, Information Systems, Technology, Opportunities & Solutions, Migration Planning, Implementation Governance, Change Management, plus ongoing Requirements Management.
- **Content FrameworkDeliverables, artifacts, building blocks, and metamodel for core entities like actors, services, data.
- Enterprise Continuum, reference models (TRM, III-RM), and Architecture Capability Framework.
- Certification via Open Group paths; no mandatory audits.
Why Organizations Use It
- Aligns strategy with IT for efficiency, reuse, and ROI.
- Reduces duplication, risks, vendor lock-in.
- Enhances governance, interoperability (Boundaryless Information Flow).
- Builds stakeholder trust through consistent standards.
Implementation Overview
- Phased, tailored rollout: foundation, pilot, scale.
- Involves maturity assessment, governance setup, training.
- Suited for large enterprises across industries; voluntary adoption.
Key Differences
| Aspect | CE Marking | TOGAF |
|---|---|---|
| Scope | Product health/safety/environmental compliance | Enterprise architecture design/governance |
| Industry | Manufacturing/EEA product sectors | All industries worldwide |
| Nature | Mandatory EU marking for regulated products | Voluntary EA methodology/framework |
| Testing | Conformity assessment/notified bodies | Architecture reviews/compliance assessments |
| Penalties | Market withdrawal/fines/recalls | No legal penalties/internal governance |
Scope
Industry
Nature
Testing
Penalties
Frequently Asked Questions
Common questions about CE Marking and TOGAF
CE Marking FAQ
TOGAF FAQ
You Might also be Interested in These Articles...

Step-by-Step Implementation Guide to ISO 27701: Building a Privacy Information Management System (PIMS) on Your ISO 27001 Foundation
Implement ISO 27701 on your ISO 27001 foundation with this actionable guide. Tackle PII controls, audit evidence, GDPR integration. Templates, checklists for 20

Thailand PDPA Implementation Guide: Subordinate Regulations for 72-Hour Breach Reporting and Cross-Border Transfers (2022-2024 Rules)
Step-by-step Thailand PDPA guide: 72-hour breach notifications, cross-border transfers (2022-2024 rules). Risk checklists, GDPR templates avoid THB 5M fines. Mu

5 Ways Modern Compliance Software Makes Evolving Regulations Your Strategic Advantage
Discover 5 ways modern compliance software turns evolving regulations into strategic advantage. Automate monitoring, cut 3x non-compliance costs, stay audit-rea
Run Maturity Assessments with GRADUM
Transform your compliance journey with our AI-powered assessment platform
Assess your organization's maturity across multiple standards and regulations including ISO 27001, DORA, NIS2, NIST, GDPR, and hundreds more. Get actionable insights and track your progress with collaborative, AI-powered evaluations.
Check out these other Gradum.io Standards Comparison Pages
ISO 20000 vs IFS Food
Dive into ISO 20000 vs IFS Food: IT service management meets food safety standards. Uncover key differences, benefits & strategies to boost compliance success now!
RoHS vs ISA 95
Compare RoHS vs ISA 95: Master hazardous substance limits for EEE compliance alongside manufacturing integration models. Boost efficiency, cut risks—unlock strategies now!
UL Certification vs FERPA
Discover UL Certification vs FERPA: Compare product safety marks & student privacy rights for seamless compliance. Unlock key differences, exceptions & strategies now.