Training: CE Conformity (English / German)
from 490,00 €
CE marking is a mandatory prerequisite for placing numerous products on the market in the European Economic Area and primarily applies to manufacturers, importers, and their authorized representatives.
In addition to compliance with the relevant product legislation, statutory requirements include conducting a conformity assessment procedure, preparing technical documentation, and issuing the EU Declaration of Conformity.
This training therefore focuses on the legal foundations and the practical implementation of CE marking.
Price Overview (Net) · 1-day
| Variant | Budget | Balanced | Premium |
|---|---|---|---|
| Open training — per participant | |||
| 1-day | 490 € | 590 € | 690 € |
| In-house — base incl. 4 participants | |||
| Base | 1.890 € | 2.190 € | 2.490 € |
| + per participant 5–8 | 290 € | 390 € | 490 € |
| + per participant 9+ | 145 € | 190 € | 245 € |
Scope of services per package
| Service | Budget | Balanced | Premium |
|---|---|---|---|
| Handout | |||
| Learning assessment + certificate | |||
| Practical exercises tailored to customer requirements |
Description
CE marking is a mandatory prerequisite for placing numerous products on the market in the European Economic Area and primarily applies to manufacturers, importers, and their authorized representatives.
In addition to compliance with the relevant product legislation, statutory requirements include conducting a conformity assessment procedure, preparing technical documentation, and issuing the EU Declaration of Conformity.
This training therefore focuses on the legal foundations and the practical implementation of CE marking.
Learning Objective
Our CE conformity assessment training provides participants with a structured, practice-oriented approach to complex statutory requirements.
You will gain an understanding of the relevant European directives, regulations, and harmonized standards, and determine which requirements apply to your specific products.
As a participant, you will acquire the knowledge required to independently prepare CE conformity assessment procedures, assess risks, compile necessary evidence, and verifiably document product conformity.
The objective is to provide you with regulatory certainty and proficiency in the practical application of CE marking.
What to Expect
From the legal foundations and the identification of applicable regulations to technical documentation and the EU Declaration of Conformity, the core elements of the CE process will be covered.
The training combines expert instruction with practical examples and exercises. Typical challenges encountered in day-to-day operations will be examined and discussed.
For in-house training courses, available for groups of 4 or more participants, content and case studies are tailored to your specific products, industry, and organizational requirements.
Short quizzes, facilitated discussions, and practical exercises facilitate knowledge transfer and ensure effective application in practice.
Content
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Foundations and significance of CE marking
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European directives, regulations, and legal acts
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Duties and responsibilities of manufacturers, importers, and authorized representatives
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Determining applicable product regulations
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Harmonized standards and their application
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Conformity assessment procedures
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Risk assessment and technical requirements
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Technical documentation
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EU Declaration of Conformity
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Requirements for CE marking and product labeling
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Placing products on the market and market surveillance
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Practical implementation based on real-world examples
Target Audience
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Manufacturers and economic operators placing products on the market
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Importers and authorized representatives
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Product compliance managers
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R&D and design engineering personnel
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Quality management and quality assurance personnel
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Technical documentation
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Procurement and sales professionals
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Supply industry and service providers
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Interested professionals
Conclusion
The training concludes with a learning assessment. This enables you to evaluate your acquired knowledge while supporting our internal quality assurance processes.
Upon successful completion of the course, you will receive a certificate verifying your acquired qualification.
Contact
Require a customized proposal or have questions? Simply contact us.
Available Dates
| Date | Time | Location | Duration | Seats |
|---|---|---|---|---|
| 11.12.2026 | 08:30–17:00 | Frankfurt am Main | 1-day | 12 |
| 27.01.2027 | 08:30–17:00 | Frankfurt am Main | 1-day | 12 |
| 07.04.2027 | 08:30–17:00 | Nuremberg | 1-day | 12 |
| 02.06.2027 | 08:30–17:00 | Braunschweig | 1-day | 12 |
| 23.06.2027 | 08:30–17:00 | Lucerne | 1-day | 12 |
| 06.10.2027 | 08:30–17:00 | Lucerne | 1-day | 12 |

Mark Haacke
Founder & Managing Director
Compliance Engineering, Type Approval, Functional Safety
For over 25 years, Mark Haacke has combined deep technical expertise with regulatory foresight. He guides manufacturers from the early conceptual phase through to market launch, translating complex regulations into technical implementation during product development and modification, product failure analysis and assessment, and the definition of corrective actions.
View Profile →Product safety
Safety instructions
"Conformity of Production" (CoP) procedures are a statutory obligation for all manufacturers of type-approved products.
This applies equally to both suppliers and manufacturers (including within multi-stage approval processes).
In the basic CoP training, you will learn all fundamental statutory requirements and how to implement them most effectively in practice.





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