Plan Your EU MedTech Clinical Trial in 5 Days (Without Guesswork)

A free webinar + crash course for sponsors preparing EU pre-market studies. 

💡 What You’ll Learn

• How MDR 2017/745, ISO 14155:2020, and MDCG guidance shape every EU clinical investigation

• How to evaluate investigators and sites for motivation, capacity, and reliable enrollment

• How national authorities and ethics committees coordinate approvals across Member States

• How to design a realistic, compliant budget that supports timelines and quality

• What operational practices sustain study performance after First Patient In