What we do:
CE marking is where the whole project comes together. It is not a final paperwork exercise but a structured conformity process with a clear beginning and end, drawing directly on the outputs of every preceding stage: the Risk Assessment Report, the safety concepts from the design phase, and the verification and validation evidence. Because one competent partner carries the work from the initial risk assessment through to the Declaration of Conformity, there are no interface gaps or hand-off risks between separate suppliers, and every conformity decision traces back to the evidence behind it.
The process runs under the Machinery Directive 2006/42/EC today and is aligned to the Machinery Regulation (EU) 2023/1230, mandatory from 20 January 2027, so machinery placed on the market stays compliant across the transition. It follows six defined steps:
- Identify the applicable legislative framework. We determine which directives and regulations apply to the machinery in scope and assess whether a Notified Body is required.
- Identify the harmonised standards. We establish the applicable Type A, Type B, and where one exists Type C standards, which provide the presumption of conformity with the applicable Essential Health and Safety Requirements.
- Carry out the risk assessment. We produce the Risk Assessment Report in accordance with EN ISO 12100, covering hazard identification, risk estimation, evaluation, and risk reduction.
- Verification and validation. We verify and validate the machine and its documentation against the applicable legislation and harmonised standards, confirming the achieved Performance Level meets or exceeds the required Performance Level (PL ≥ PLr) and evidencing each Essential Health and Safety Requirement.
- Assess conformity and compile the documentation. We confirm the applicable conformity assessment route and compile the complete Technical Documentation, combining our reports with the documents supplied by the customer.
- Sign the Declaration of Conformity and affix the CE mark. The Declaration of Conformity and CE mark are issued to the manufacturer for signature and application to the machine, who then retains the Technical Documentation for a minimum of ten years.
Because the documentation is authored and peer-reviewed by CMSE and CECE-qualified engineers and built progressively throughout the project, the result is a complete, audit-ready Technical Documentation set, defensible under market surveillance rather than assembled retrospectively
Summary
Machine safety
Machine safety means spotting risks before they cause harm, to your people or to your budgets and production not just checking compliance boxes. Your safety team reviews equipment changes early, updating or creating safeguards as needed. This proactive step happens before problems arise, so your project finishes safely and on track.
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Our service works look like this
Machine Safety Services
Risk Assessment Report
Following EN ISO 12100, we take your machine from limit definition through hazard identification to effective risk reduction, bringing risk down to an acceptable level in line with the state of the art.
Technical Documentation
A structured, audit-ready dossier developed throughout the project lifecycle, capturing all required compliance documentation and engineering evidence. Finalised at completion to support the client’s Declaration of Conformity.
Safety – Front End Engineering Design Study
A front-end engineering design process that translates identified risks into practical, costed solutions. Each hazard is paired with a defined concept, implementation roadmap, and budget estimate to support informed decision-making.
Safety Design & Implementation
Detailed safety engineering covering functional safety specification, electrical and hardware design, safety PLC programming, and system integration to deliver compliant, robust, and maintainable safety solutions.
Safety Verification & Validation
A rigorous testing and evaluation process confirming that all safety measures have been correctly implemented and perform as intended, in line with standards such as EN ISO 13849 and EN 60204-1.
Authorised Representative
Non-EU machinery manufacturers need an EU-based representative to place machinery on the European market.
Sitewide Machinery Risk Prioritisation
For sites with dozens or hundreds of machines, the challenge is rarely identifying a single issue. It is knowing where to start.


