Coauthor by Hindsight, a compliance software provider tailored for medical device development, has announced a new lunchtime webinar series on medical device cybersecurity.
The series is designed to assist manufacturers, regulatory affairs specialists, and software developers in meeting evolving cybersecurity requirements, including FDA, MDR, and IEC 81001-5 standards.
The first session, happening on Thursday, 13th February 2025, will provide insights into critical regulatory updates and integrating cybersecurity within QMS. Topics to be discussed include:
· The latest regulatory requirements and their impact on cybersecurity practices.
· How cybersecurity enhances patient safety and ensures compliance.
· Myths and misconceptions that may delay regulatory approval.
· Practical updates to SOPs to align QMS with cybersecurity needs.
This brief, 30-minute session is a must for professionals looking to balance compliance with development efficiency. Participants will gain insights from industry experts in regulatory and software development, with a live Q&A for addressing specific challenges. The webinar will be led by Alan Parkinson, CEO of Hindsight Software, alongside co-host Dr Heather Carre-Skinner, a specialist in Regulatory & Quality Compliance for Medical Devices and SaMD.
Upcoming sessions in the series include:
· Threat Modelling – Effective ways to identify and mitigate cybersecurity risks.
· Software Supply Chain & SBOMs – Managing vulnerabilities while ensuring compliance.
· Security Testing – Best practices for penetration testing and secure code review.
Register today!
The webinar is free, but spots are limited. Reserve your place now at: https://www.coauthor.app/webinars
