Coauthor by Hindsight, a software solution tailored for compliance in medical device development, has introduced a new lunchtime webinar series dedicated to addressing medical device cybersecurity.
The series is specifically designed to help manufacturers, regulatory professionals, and developers navigate the increasingly complex cybersecurity requirements, including FDA regulations, MDR guidelines, and IEC 81001-5 standards.
The first webinar, set for Thursday, 13th February 2025, will focus on recent regulatory changes and the integration of cybersecurity into QMS processes. Topics to be covered include:
· Emerging regulatory requirements and their impact on cybersecurity.
· Cybersecurity’s role in ensuring patient safety and device compliance.
· Misconceptions that could hinder the approval process.
· Actionable updates to SOPs and strategies for incorporating cybersecurity into QMS.
This 30-minute session is ideal for professionals who want to maintain compliance without disrupting their development workflows. Attendees will hear from experts in regulatory and software development and can participate in a live Q&A session to address specific concerns. The webinar will be led by Alan Parkinson, CEO of Hindsight Software, and co-hosted by Dr Heather Carre-Skinner, a prominent expert in Regulatory & Quality Compliance for Medical Devices and SaMD.
Future webinars in the series will cover:
· Threat Modelling – Approaches to identifying and mitigating risks.
· Software Supply Chain & SBOMs – Addressing vulnerabilities and ensuring compliance.
· Security Testing – Practical guidance on penetration testing, threat verification, and secure code reviews.
Sign up now!
This free webinar has limited availability. Register here: https://www.coauthor.app/webinars
