Regulatory Affairs for Medical Devices – EU MDR and IVDR
 Regulatory Intelligence
 Paper
 Tools and Services
 Features for success
 RA Assistant
 Your Professional Partner
  
Regulatory Affairs Assitant – Elly
  
 TEST ELLY NOW  
GLOBAL REGULATORY
 KNOW-HOW
 AT YOUR FINGERTIPS
  
What are the main Use-Cases of Elly:
- Up to date on Regulations and Guidelines of 35+ Countries
- Communicate with 1000’s of regulatory-related documents
- Create Initial Regulatory Assessments with One Click
- Get Assistance in creating the Intended Purpose
- Get Assistance in classifying the product under EU MDR/IVDR and FDA
  
  
IT INCLUDES: Complete MDR, Complete IVDR, New published EU documents, MDR / IVDR implementation guide