Webinars

Webinars

Webinars

Past sessions

  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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!

Past sessions

  • 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • 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!