Coauthor by Hindsight, a developer-friendly compliance software solution for medical device development, is launching a new webinar series focused on medical device cybersecurity.
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.
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.
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.
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