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CE marking Online CE marking software
General and detailed information about CE marking, such as documentation and testing. We discuss Declaration of Conformity, Technical File, harmonised standards, and European directives.
General
- Applying the new UKCA marking on products
- Top 21 Myths About PPE (Personal Protective Equipment)
- 8 Factors You Must Consider When Selecting an EMC Antenna
- Affixing CE Marking On Products And How To Avoid Doing It Wrongly?
- What are the weaknesses in the CE marking system?
- What are the opportunities for improving customer information?
Directives
- 8 Types of Personal Protective Equipment (PPE)
- What is a European directive?
- Toy Safety Directive 2009/48/EC in Details
- RoHS Directive (2011/65/EU) in Details
- PPE Directive (EU) 2016/425 in Details
- Electromagnetic Compatibility (EMC) Directive 2014/30/EU in Details
European standards
Product testing
- 11 Types of Medical Device Design Testing
- 7 tips to help you pass your EMC compliance test
- Six reasons you fail Low Voltage Directive (LVD) compliance testing
- Types of product testing under the EMC Directive
- Accredited and non-accredited testing: Low Voltage Directive
- Conformity Assessment Module F
Risk assessment
- 8 Tools For Medical Device Quality Control
- What is Risk Assessment and Control Table (RACT)?
- Medical Devices: Risk Management Process in 7 Steps
- Medical Device Risk Evaluation And How To Determine The Risk Acceptance Criteria
- The BXM Method in the Safety Risk Management for Medical Devices
- 3 Methods for Risk Estimation
Notified bodies
Technical file
Declaration of Conformity
Others
- 8 Things You Must Consider When Designing And Constructing An Industrial Product
- How To Develop A Verification Method For Your Design Verification Process
- Design Verification Process for Medical Devices: All You Need To Know
- Medical Device Safety: 5 Methods for Safety Cost Estimation
- Classification Of Medical Devices And Their Routes To CE Marking
- How To Be Sure Your Hoverboard Is Safe