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THE CLEVER COMPLIANCE BLOG

THE CLEVER COMPLIANCE BLOG

A blog about product compliance, certification, and product markings.

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Featured Posts

product compliance dashboard and reporting

4 Benefits of a Product Compliance Dashboard for CCOs

on 2020-09-152021-12-21General product compliance
eu authorised representative mandate and responsibilities

Responsibilities and Mandate of an EU Authorised Representative

on 2021-03-032021-12-21CE marking

4 Tips to Improve Product Compliance Management in the Workplace

on 2020-09-092021-12-21General product compliance

Market Surveillance Regulation (EU) 2019/1020: Does It Apply to You?

on 2021-03-092021-12-21General product compliance

6 Tips for Successfully Managing Supplier Compliance

on 2020-12-152021-12-21General product compliance
on 2021-11-032021-12-21Electrical product compliance

Top EEE Constructional “Rules of Thumb” Regarding EMC Compliance

This article provides readers with a list of the best EEE constructional practices for ensuring EMC compliance.

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on 2021-11-032021-11-30General product compliance

Understanding REACH

This article provides information on the REACH Regulation and what duty holders need to do to register a chemical substance with ECHA.

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on 2021-11-022021-11-30Medical product compliance

Usability Engineering in Medical Devices: Definition, Standards & Tools

This article focuses on usability engineering in medical devices. Information regarding relevant safety standards is also provided.

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on 2021-11-022021-12-21Medical product compliance

Medical Device Risk Management Glossary

This glossary includes some of the most commonly used terms in medical device risk management.

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on 2021-10-282021-12-21Medical product compliance

What is Benefit-Risk Analysis (BRA) of Medical Devices? Definition, Factors & Guidance Documents

This article provides readers with information on what benefit-risk analysis is, how to evaluate the benefits and risks of a medical device, and what guidance documentation to use.

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on 2021-10-272021-12-21Electrical product compliance

Documentation Requirements for EMC Testing

This article provides electrical and electronic equipment manufacturers with a list of all documentation requirements for performing EMC testing.

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on 2021-10-272021-12-21Electrical product compliance

What is EMC Testing? Definition & Types of Tests

This article explains what EMC testing is and provides readers with information on the different types of EMC tests electrical products must pass.

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on 2021-10-262021-12-21Electrical product compliance

Routine Tests Explained: Definition, Procedure, Standards & Test Records

Learn here what a routine test is, how to perform it and what standards to use. Get also a free template of a test record sheet for recording test results.

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on 2021-10-212021-12-21Medical product compliance

ISO 14971 – A Risk Management Standard for Medical Devices

There are several safety standards that address medical device safety. Some of them are ISO 14971, IEC 60601-1, IEC 62366 and ISO 10993-1. This article focuses on ISO 14971, a widely recognized risk management standard for medical devices.

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on 2021-10-152021-12-21Electrical product compliance

7 Types of Power Source Components for Electrical Products

Read this article to learn about the different types of power sources components, which are the most important part of any electrical product.

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Popular Posts

medical device standalone software ce marking guide - MDR and IVDR
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on 2020-03-122021-12-21
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FDA Approval Process for Medical Devices: Step-by-Step Guide

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EU MDR Labelling Requirements for Medical Devices

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