Description: From this poster presentation, the visitors will get an overview of regulatory requirements for Risk Management, Clinical Evaluation and Post Market Surveillance for aiding compliance with MDR. They will also be able to identify and improve on various areas of data redundancy with the help of digitization. Nevertheless, participants will also be able to get an insight view on integration between these systems.
Learning Objectives:
1. Upon completion, participants will be able to list the requirements for Risk Management, Post Market Surveillance and Clinical Evaluation of a medical device according to Regulation (EU) 2017/745.
2. Upon completion, participants will be able to determine the pain point areas of data redundancy and technical documentation inconsistencies.
3. Upon completion, participants will be able to tackle the current processes and improve their technical documents with the help of digitization.
