In our first episode, we will discuss the importance of the device description and the link to the other standalone documents, such as classification, GSPRs, regulatory compliance plan, instructions for use and the list of applicable standards. This will enable you to start out on the right foot with your medical device development project. 
We hope you find this series helpful! You are so welcome to let us know your thoughts and if you have any questions by commenting below or emailing us at QmedPodcast@gmail.com.