Online Panel Discussion: Navigating Regulatory Approval for Medical Devices

Regulatory approval is the final and most critical step before launching a medical device — but getting there efficiently is becoming increasingly complex.  

In this upcoming webinar, UL Solutions experts will explore how manufacturers can navigate global regulatory requirements more effectively, with a focus on medical device cybersecurity, electrical safety and certification strategies.* 

Key takeaways

During the webinar, UL Solutions experts will discuss key questions and practical considerations for medical device manufacturers preparing for compliance, such as:

• How can medical device regulatory requirements be met efficiently before launch?
• Is there a single global standard for medical device cybersecurity?
• Are electrical safety requirements still a real challenge — or just a formality?
• How can manufacturers achieve global compliance faster and at lower cost?
• Do regulators prefer certified results over standalone test reports? 

Speakers

Maurizio La Mura, engineering manager, Consumer, Medical and Information Technologies, UL solutions  

Marcin Wagner, business development manager, Consumer, Medical and Information Technologies, UL solutions

Fergus Wong, Product/Service Specialist, Consumer, Medical and Information Technologies, UL solutions 

* Within UL Solutions we provide a broad portfolio of offerings to all the medical device industries. This includes certification, Approved/Notified Body and consultancy services. In order to protect and prevent any conflict of interest, perception of conflict of interest and protection of both our brand and our customers brand, we have processes in place to identify and manage any potential conflicts of interest and maintain impartiality. UL Solutions is unable to provide consultancy services to EU MDD, MDR, IVDD or IVDR Notified Body, UKCA MD Approved Body or MDSAP Customers.