Complife Academy
Your Training, Your Rules: Start Whenever You Want, Wherever You Are.
Discover our On Demand courses for professionals who work, or aim to work, in Medical Devices, Cosmetics, Nutraceuticals or Pharma markets.
eLearning
Complife Academy lessons are developed by our experts and designed for those who want to learn independently, at their own pace, without calendar constraints.
The new on-demand video course platform is designed to offer educational content that is always accessible and up-to-date, assuring maximum flexibility.
How to Register in EUDAMED: Operational Guidance
EUDAMED is the European database for medical devices and represents one of the key elements introduced by Regulation (EU) 2017/745 (MDR). The database integrates several modules to collect and track all devices placed on the EU market and the Economic Operators involved, operating alongside the national ministerial databases of individual Member States.
Do you already know how to register your medical devices in EUDAMED?
Implementation of Regulation (EU) 2017/746 on IVDs (IVDR)
The course is dedicated to understanding and applying Regulation (EU) 2017/746 (IVDR), which has redefined the European regulatory framework for in vitro diagnostic medical devices.
The objective is to provide a clear overview of the regulatory, organizational, and documentation-related implications introduced by the IVDR, highlighting how companies must structure processes, responsibilities, and control systems to ensure compliance with the new requirements.
Clean Rooms: Managing Classified Production Environments
Classified production environments are critical for ensuring the quality and safety of medical devices. Managing a clean room requires careful attention to environmental controls, operational protocols, maintenance, and staff training.
A structured, well-documented approach to clean room management is essential to ensure safe processes, minimize risks, and maintain regulatory compliance.
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