Last Updated on: 21st January 2025, 07:25 am
Coauthor by Hindsight, a compliance software solution designed with medical device developers in mind, has announced the launch of a webinar series centred on medical device cybersecurity.
This new series of lunchtime webinars aims to assist medical device manufacturers, regulatory professionals, and software developers in navigating the ever-changing cybersecurity requirements, including those outlined by the FDA, MDR, and IEC 81001-5 standards.
The inaugural session, scheduled for Thursday, 13th February 2025, will explore key regulatory changes and integrating cybersecurity within QMS. Topics covered will include:
· The most recent regulatory demands and their implications for cybersecurity.
· How cybersecurity contributes to patient safety and device compliance.
· Common misconceptions that could obstruct regulatory approval.
· Practical guidance for updating SOPs and aligning cybersecurity with QMS.
This 30-minute session is designed for professionals seeking to maintain compliance while streamlining development processes. Attendees will gain expert knowledge from specialists in regulatory affairs and software development, along with the opportunity to participate in a live Q&A session addressing real-world challenges. The session will be led by Alan Parkinson, CEO of Hindsight Software, alongside Dr Heather Carre-Skinner, an authority on Regulatory & Quality Compliance for Medical Devices and SaMD.
Further sessions in the lunchtime series will include:
· Threat Modelling – Strategies for identifying and mitigating cybersecurity risks.
· Software Supply Chain & SBOMs – Addressing vulnerabilities and ensuring compliance.
· Security Testing – Exploring penetration testing, threat verification, and secure code review.
Register now!
The webinar is free to join, but places are limited. Secure your spot at: https://www.coauthor.app/webinars
