How medical software teams break the regulatory bottleneck

Every medical device you ship needs a decade of security updates, maintenance, and regulatory upkeep. Each new product adds another decade. When every product runs on its own technology, your team repeats the same regulated work again and again. The few people who can safely change a released product are also the people your next launch needs.

In 45 minutes, Annika Packalén talks with Roger Mazzella and Venla Pouru about how a shared software foundation cuts that repeated work, and where it doesn’t.

You’ll learn:

• Why a regulated portfolio gets harder to maintain as it grows
• What a common software foundation can realistically cover
• How to bring consistency to products already in clinical use
• Build, open source, or buy: what each choice asks of you over a device’s lifetime
• How to answer the pressure to get to market faster

Who should join: Software, R&D, and product leaders at medical device manufacturers who’re responsible for developing highly regulated, long-lived medical software applications and devices.

Live on October 29 at 15:00 CET. Can’t make it? Register anyway and we’ll send you the recording.