General CE marking information
Information about European directives, both CE marking directives and other directives
Information about harmonised and non-harmonised European standards
Information about testing your product, both CE mark testing and testing in general
What is a notified body and do you need a notified body?
What is a technical file and how do you create a technical file?
Declaration of Conformity
What is a Declaration of Conformity, how do you create one, and what needs to be in a Declaration of Conformity?
- 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?
- What are RAPEX and ICSMS?
- What is the CE mark?
- Validate a CE mark
- 8 Types of Personal Protective Equipment (PPE)
- What is a European directive?
- The Road Towards The New Hazard-Based Safety Standard EN 62368
- How To Select The Correct Standards For Your Product’s Compliance Process
- How Is A Harmonised Standard Made?
- What is a harmonised standard?
- 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
- 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
- 5 Tools for Performing Medical Device Risk Analysis
- 5 Critical Factors Important To Medical Device Risk Assessment
- What Are The Hazards Associated With Machinery and Equipment?
- What are the hazards related to products falling under the Machinery Directive (MD)?
- What are the hazards related to products falling under the Low Voltage Directive (LVD)?
- What are the steps of the risk assessment?
- What are the phases of the risk assessment?
- What is a risk assessment methodology?
- All You Need To Know About The Unannounced Audit Visit From A Notified Body
- 5 Things To Consider When Choosing A Notified Body For Your Product’s Conformity Assessment
- What is a notified body?
- What is a technical file?
- Selling on Amazon: How to get the Declaration of Conformity in 1 day?
- What is a Declaration of Conformity?
- 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