Each table runs 3 times (9:45 am, 10:45 am & 11:45 am) on the same topic. Tables are exclusive, other vendors cannot attend. Minimum 10 participants for each table.
Attendees can select up to 3 roundtables.
- Direct-to-Patient Clinical Trials and the unique considerations for Medical Devices
- Patient Recruitment, Retention, and Engagement
- Expanding clinical trials into emerging markets
- Inspection Readiness and passing inspections
- Post market data collection & Data Security (Cybersecurity)
- Key considerations in clinical trials for wearable devices
- Latest technology and its impacts on Medical devices – 5G, virtual reality, AI, wearables
- Clinical site management
- IRT in Supply Chain Management
- Clinical Trials for combination devices
- Dealing with disruption: Look back at 2020 and how to adapt trials to keep them running in disrupted times
- CRO selection at all points of the Medical Device study lifecycle
- The impact of the new MDR regulation on the European medical device industry
