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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 2022-09-162022-09-16General product compliance

UKCA Marking vs CE Marking – FAQ

This article provides detailed information on the UKCA marking and how the new UK conformity marking differs from the EU CE marking.

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on 2021-12-142021-12-21General product compliance

Exporting to Saudi Arabia: Product Certification & the SASO Saber System

This article focuses on import procedures in Saudi Arabia and what foreign manufacturers need to do to pass customs and sell their goods in the country. It also provides information about the SASO Saber system.

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on 2021-12-132021-12-14General product compliance

Understanding the Moroccan Cم (CMIM) Mark

This article provides manufacturers with information on the Moroccan Cم (CMIM) mark and lists some digital sources where they can stay updated with the changes in the local legislation.

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on 2021-12-082022-09-16General product compliance

Understanding the UKCA Marking

This article provides detailed information on the new conformity marking required for products sold on the market in Great Britain.

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on 2021-11-302021-11-30Medical product compliance

Misbranded & Adulterated Medical Devices – FDA

This article provides brief information on misbranded and adulterated medical devices.

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on 2021-11-252021-12-21Electrical product compliance

Safety-Critical Components: General Information & Relevant UL Standards

This post contains information on what safety-critical components are and a list of UL standards applicable to various safety-critical parts implemented in the design of electrical equipment.

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on 2021-11-182021-12-21Medical product compliance

11 Severe FDA Compliance Actions & Penalties

This article provides information on all FDA’s compliance actions and penalties, including product recalls, disqualification, civil money penalties and seizure.

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on 2021-11-112021-12-21Medical product compliance

Understanding the BXM Method

This article clarifies what the BXM method is and why medical device manufacturers should use it when performing risk management.

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on 2021-11-102021-11-30General product compliance

What is Pre-control and Positrol Verification?

Pre-control and positrol are two methods manufacturers need to use to verify the supplier quality process performance. This article provides readers with brief information on each of these methods.

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on 2021-11-102021-11-30General product compliance

7 Elements Essential for Product Liability Prevention

Product liability prevention is about understanding what to do and how to do it to achieve product safety excellence. For that reason, this article provides information on what product liability is and how to prevent it.

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Recent Posts

  • UKCA Marking vs CE Marking – FAQ
  • Exporting to Saudi Arabia: Product Certification & the SASO Saber System
  • Understanding the Moroccan Cم (CMIM) Mark
  • Understanding the UKCA Marking
  • Misbranded & Adulterated Medical Devices – FDA

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Popular Posts

medical device standalone software ce marking guide - MDR and IVDR
Medical product compliance

CE Marking Medical Device Standalone Software – MDR & IVDR Guide

General product compliance

Product Labelling Requirements for Europe

CE marking

Declaration of Conformity Guidance & Template

on 2020-03-122021-12-21
Medical product compliance

FDA Approval Process for Medical Devices: Step-by-Step Guide

Medical product compliance

EU MDR Labelling Requirements for Medical Devices

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