Learn here what qualities distinguish good from bad suppliers.
This article describes four approaches experienced importers use to address unacceptable product defects in a shipment.
Check this article for guidance on how to prepare a SCIP dossier.
Don’t know what compliance metrics to use for keeping track of your product compliance activities? Read this article to find out.
Read this article to learn what a compliance report is, why your organisation needs such a report, and what kind of information it should include.
This article presents five reasons why risk management is important and information on how to ensure you make risk-free medical devices.
Learn what a medical device risk management plan is and how to create one.
This blog post presents the most common electromagnetic compatibility issues found in electrical equipment.
This article answers questions, such as “What is a standard?”, “What are EN, ISO and IEC standards?” and “How to select the correct safety standards?”.
The following glossary contains key compliance terms and definitions that any new compliance professional must know before diving into the complex regulatory framework for the first time.