STAFFORDSHIRE, UK. January 20th, 2025 – Coauthor by Hindsight, a developer-friendly compliance software solution for medical device development, is launching a new webinar series focused on medical device cybersecurity.
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This new series of lunchtime webinars is designed to help medical device manufacturers, regulatory affairs professionals, and software developers navigate evolving cybersecurity requirements, including FDA, MDR, and IEC 81001-5 requirements.
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The first webinar, taking place on Thursday, 13th February 2025, will address critical regulatory updates and QMS Integration; providing practical insights on how to embed cybersecurity within QMS and covering topics such as:
·     The latest regulatory requirements and their impact on cybersecurity.
·     The role of cybersecurity in patient safety and medical device compliance.
·     Common myths and misconceptions that could hinder regulatory approval.
·     Practical updates to SOPs and plans to align cybersecurity with QMS.
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This 30-minute webinar is essential for professionals looking to ensure compliance while maintaining efficient development workflows. Attendees will benefit from expert insights from regulatory and software development specialists and a live Q&A session to address specific challenges. Led by Alan Parkinson, CEO, Hindsight Software, the webinar will be co-presented by Dr. Heather Carre-Skinner, a leading expert in Regulatory & Quality Compliance for Medical Devices and SaMD.Â
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Coauthor by Hindsight will host additional sessions in this informative lunchtime series, covering:
·     Threat Modelling – How to identify and mitigate cybersecurity risks.
·     Software Supply Chain & SBOMs – Managing vulnerabilities and compliance.
·     Security Testing – Penetration testing, threat verification, and secure code reviews.
Register today!
The webinar is free to attend, and places are limited. Register today at: https://www.coauthor.app/webinars