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

In this webinar, Chris Rush from @GreenlightGuru discusses 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. Listen in to learn 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.