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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 or IVDD Notified Body, UKCA MD Approved Body or MDSAP Customers.
Nov 5, 2026
  • Webinar

Medical Devices: Navigating Wireless Regulatory Requirements

Adding wireless technology to a medical device? Learn how to navigate global certifications, modular approvals and market access requirements and plan a clearer path from design to launch.

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Date & Time

Starts

Nov 5, 2026 10:00am CST

Ends

11:00am CST

Language

English

8:00 a.m. Los Angeles | 11:00 a.m. New York | 5:00 p.m. Milan

Build a clearer path to global market access for wireless medical devices.

Join UL Solutions experts to learn how to plan for wireless certification, modular approvals and global market access from the start.

Wireless capabilities are transforming medical devices into connected healthcare solutions and Internet of Medical Things (IoMT) ecosystems. They enable remote monitoring, asset tracking, data sharing and interoperability across care environments, but can also introduce additional radio, certification and market access requirements that affect design decisions, development costs and launch timelines.

In this practical webinar, UL Solutions experts will examine the global wireless regulatory landscape for connected medical devices.

You will explore how wireless module integration can impact compliance obligations, where modular approvals can help and what to consider when pursuing certification and type approval in the United States, Europe and other international markets.

What you will learn

  • How Bluetooth®, Wi‑Fi, cellular, RFID and other wireless technologies can affect medical device regulatory and compliance requirements.
  • How to assess the benefits and limitations of modular approvals when integrating wireless modules.
  • Key wireless certification and type approval considerations for the United States, Europe and other global markets.
  • Common compliance challenges that can impact development schedules, product launches and market access.
  • Practical ways to plan wireless certification and regulatory approval activities earlier in the product lifecycle.

Reserve your place

Register now to gain practical insight that can help your team anticipate wireless compliance needs, make informed design decisions and prepare for global market access. Cannot attend live? Register to receive access to the webinar recording.

Moderator: Maja Bland, senior product/service specialist, Consumer, Medical and Information Technologies

Speaker: Mark Briggs, operations director, Consumer, Medical and Information Technologies

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