Coauthor by Hindsight, a developer-focused compliance software platform for medical device creation, has launched a new lunchtime webinar series dedicated to medical device cybersecurity.
This educational series aims to support medical device manufacturers, regulatory affairs teams, and software developers in understanding and meeting evolving cybersecurity standards, including FDA, MDR, and IEC 81001-5.
The first session, taking place on Thursday, 13th February 2025, will focus on significant regulatory updates and the integration of cybersecurity into QMS. Key topics to be discussed include:
· The newest regulatory requirements and their effects on cybersecurity.
· The importance of cybersecurity in patient safety and device compliance.
· Widespread myths that could complicate the regulatory approval process.
· Practical adjustments to SOPs and plans to ensure QMS incorporates cybersecurity.
This concise 30-minute webinar is an excellent resource for those looking to balance regulatory compliance with development efficiency. Participants will gain valuable insights from experienced regulatory and software development professionals and can engage in a live Q&A session to address individual challenges. The event will be hosted by Alan Parkinson, CEO of Hindsight Software, with co-presenter Dr Heather Carre-Skinner, a recognised leader in Regulatory & Quality Compliance for Medical Devices and SaMD.
Additional webinars in this series will explore:
· Threat Modelling – Recognising and addressing cybersecurity risks.
· Software Supply Chain & SBOMs – Managing vulnerabilities while staying compliant.
· Security Testing – Best practices in penetration testing, threat verification, and secure coding.
Don’t miss out!
The webinar is free to attend, but spaces are limited. Register now at: https://www.coauthor.app/webinars
