Webinars
Webinars
Past sessions
What was discussed in the webinar
- Why Preparation is Key! – Learn what to do before beginning a grant
- Write with consideration for the appropriate tone and mindset.
- Understand the importance of strategic communication.
What was discussed in the webinar
- In this webinar, we will discuss common mistakes in planning and conducting a PMCF study and how to avoid them.
- The speaker will share his personal experience as a tutor for a notified body.
- Q&A session where your questions will be addressed.
What was discussed in the webinar
- Obtaining data excellence for more impactful research outcomes
- Strategies for collecting and managing quality clinical trial data according to the CDISC guidelines
- The future perspectives of data collection
- Q&A session where your questions will be addressed.
What was discussed in the webinar
- The relationship between Post-Market-Clinical-Follow-up, Post Market Surveillance Activities, Clinical Evaluation Risk Management File and the feedback from the market
- The relevant documents required, for example, the MDCG Guidance documents for Medical Devices and the In Vitro Diagnostic
- How to create a Post-Market-Clinical-Follow-up Plan and Report
- Q&A session where your questions will be addressed.
What was discussed in the webinar
- Gain a comprehensive understanding of Innosuisse criteria and the evaluation process.
- Acquire actionable advice to enhance the quality of your funding application, and avoid common pitfalls.
- Q&A engagement where your specific questions will be addressed.
What was discussed in the webinar
- Learn from a professional expert in the MedTech industry!
- Get expert insights and practical tips for smooth CE marking implementation and ongoing compliance maintenance.
- Find out what are the essential documentation requirements.
- Engage in Q&A sessions and get personalized answers!