Learn what a medical device risk management plan is and how to create one.
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.
This article provides clarity on what a compliance program is and what elements it consists of.
This article provides clarity on what a compliance management system is, what elements it includes and what benefits it brings to companies.
Read this article to learn about the main challenges in ensuring product safety.
Read this guide to learn about the mandatory and voluntary product certification markings for goods placed on the European market.
Check this step-by-step guide to learn how to meet SCIP requirements, and learn if the SCIP regulation actually applies to you.
Duty holders must consider three types of information requirements for SCIP notifications: mandatory, required and optional. Learn more here.
Poor supplier compliance management can result in unforeseen compliance issues. Here are 6 tips to help you improve your supplier compliance.
SCIP is the new database for storing safe-use information on substances of very high concern (SVHCs) in articles as such or in complex objects.