Webinar Features
UK Post Market Surveillance Regulations: What You Need to Know Now
Learn in this on-demand webinar about the purpose of the new regulations, the key changes, and the differences and impact on CE-marked medical devices in the UK.
Format
On-Demand Webinar
Level
Basic
Trainer
Dennis Sarwin and Melissa Smits
Certificate
Certificate of Participation included
Duration
1 hour
Price
Free
Comprehensive Regulatory Expertise
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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
Dennis Sarwin
Dennis Sarwin joined Qserve in May 2022 as a Regulatory Affairs Associate, bringing experience from medical device companies and expertise in global registrations, ISO 13485, and medical device development, backed by a Double Master of Science degree in Integrated Product Design and Biomedical Engineering from TU Delft.
Meet the Trainer
Melissa Smit
Melissa joined Qserve in 2019 and, with her strong administrative and service-oriented skills, has supported the Global Registration Team since 2021, specializing in the UK Responsible Person Service and global medical device and IVD registrations by coordinating submissions, managing documentation, and ensuring compliance across various national databases.
