Medical device cybersecurity now: FDA Rules vs EU MDR—are you ready?
Join us for an exclusive webinar with Jose Bohorquez, cybersecurity expert and founder of Bold Type and CyberMed, as he demystifies the latest FDA and EU MDR cybersecurity requirements for life sciences companies. Discover how to navigate regulatory differences, integrate secure product development practices, and protect your organization from emerging cyber threats. Don’t miss this opportunity to turn cybersecurity into a strategic advantage for your business!
Patient data has become a prime target for hackers. Ransomware, DDoS botnets, data breaches… the list goes on.
To beat them to it, you need a proactive cybersecurity strategy built into every stage of your product development.
And as always, we are happy to provide! Join this training to learn how to:
- Understand FDA premarket and postmarket submission rules
- Compare FDA vs. MDR/MDCG cybersecurity expectations
- Embed SPDF across the Total Product Lifecycle (TPLC)
- Justify cybersecurity investments to leadership
- Conduct threat modeling and risk assessments effectively
You’l hear from Jose Bohorquez, MedTech cybersecurity specialist, who offers cybersecurity guidance to companies, helping them submit to the FDA with confidence and launch without delays.
Angel Buendía, Scilife’s Knowledge Manager, will be moderating this online session.
📅 August 26th, 2025 | 16:00H (CEST)
Let’s put patient safety and company reputation first, beyond checkboxes and compliance fluff.