Webinar Features
How MedTech Scale-Ups Can Stay Ahead of Regulatory Change
This on-demand webinar on Regulatory Intelligence for MedTech scale-ups highlights the importance of staying current with regulations for global compliance, and covers key automation solutions, including their risks and benefits.
Format
On-Demand Webinar
Level
Beginner
Trainer
Olena Hoi and Cécile Rosset
Exam
Certificate of Participation included
Duration
1 hour
Price
Free
Comprehensive Regulatory Expertise
Our on-demand webinars offer a flexible and valuable source of expert insights, allowing you to stay informed at your own pace.
Watch on-demand webinars at your convenience, allowing you to fit learning into your schedule without missing essential information.
Flexible Viewing
Gain insights from industry experts and stay updated on the latest trends and regulations without the need to attend live sessions.
Access to Expertise
Meet the Trainer
Olena Hoi
Olena is a seasoned Quality and Regulatory Affairs Consultant at Qserve Group with extensive experience in managing Quality Management Systems, conducting audits, and authoring regulatory submissions for high-risk medical devices across global markets, particularly in the EU under MDR and MDD regulations.
Meet the Trainer
Cécile Rosset
Cécile Rosset, MSc, is a Senior Consultant Regulatory Affairs at Qserve with over 20 years of experience in quality and regulatory affairs for Class I to III medical devices, specializing in MDR certification, technical documentation, regulatory strategy, post-market compliance, and Notified Body interactions.
