Challenges of Clinical Data Collection in MedTech, and Why It's Worth It

In this webinar, we will discuss regulatory requirements for clinical data collection for varying device classes, the challenges associated therein, and best practices for successfully planning and delegating the duties involved in running a study. We will discuss how to engage with partners, software vendors, and provide an answer to the question: “Is this all worth it?”  

Key takeaways: 

• Why collecting data for Class II and Class III devices is valuable 
• Timeline/cost challenges for running clinical studies
• How to efficiently plan and delegate activities for data collection, including CRO and EDC software selection  

About the speaker: Chris Rush is a biomedical engineer and has been in the medical device space for about 13 years. He spent a number of years managing clinical studies for Class III devices in Pivotal studies, PMA studies, and post-market registries. He is currently working as a Solutions Engineer at Greenlight Guru where he showcases the value of our Clinical Data Capture software to prospects.