Cyber Threats Lurking in Medical Devices: 2024-25 Compliance with IEC 62304
Protect Patient Safety by Mastering Cybersecurity and Compliance Strategies for 2024-25!
Instructor :
Carolyn Troiano
Webinar ID:
12440
Date: DEC 27, 2024 (FRI)
Start Time: 10 AM PT - 11:30 AM PT
Duration: 90 Mins.
Buy This Course in a Pack of 2 courses at 25% Discount HERE:
đź’» The Software Integrity Duo: Secure, Validate, and Comply
“Ensure Robust, Secure, and Compliant Software Operations Across Your Organization!”
2 Courses Included:
-
- Cyber Threats Lurking in Medical Devices: 2024-25 Compliance with IEC 62304 (duration 90 mins), find out more details here
- 2-Day Virtual Boot Camp From Fundamentals to Advanced: Your Complete Guide to Computer System Validation (CSV) Mastery (scheduled for Dec 10-11, duration 12 hrs), find out more details here
Why Pack Them Together? These courses complement each other by covering two critical aspects of software compliance: cybersecurity and validation. They provide a holistic view on ensuring medical device software meets the latest compliance requirements and is secure from threats.
Why Buy the Pack?
-
- Integrated Software Compliance Solution: Address both cybersecurity and system validation to safeguard your software from vulnerabilities while ensuring compliance.
Buy This Course in a Pack of 2 courses at 25% Discount HERE:
đź’» The Software Integrity Duo: Secure, Validate, and Comply
“Ensure Robust, Secure, and Compliant Software Operations Across Your Organization!”
2 Courses Included:
-
- Cyber Threats Lurking in Medical Devices: 2024-25 Compliance with IEC 62304 (duration 90 mins), find out more details here
- 2-Day Virtual Boot Camp From Fundamentals to Advanced: Your Complete Guide to Computer System Validation (CSV) Mastery (scheduled for Dec 10-11, duration 12 hrs), find out more details here
Why Pack Them Together? These courses complement each other by covering two critical aspects of software compliance: cybersecurity and validation. They provide a holistic view on ensuring medical device software meets the latest compliance requirements and is secure from threats.
Why Buy the Pack?
-
- Integrated Software Compliance Solution: Address both cybersecurity and system validation to safeguard your software from vulnerabilities while ensuring compliance.
- Hands-On, Practical Learning: Gain real-world insights and techniques that can be applied immediately to improve system security and compliance processes.
- Bundle Savings: Receive both courses at a discounted rate, making it an excellent value for professionals responsible for software compliance.
Note: Do you want to custom design your pack and choose courses of your choice? Just drop us an email at support@compliancemeet.com or call at Toll Free: +1 (888) 959-4972. We’ll be happy to help you!
           Buy Both Courses at a 25% discount HERE
What will you learn
-
- Importance Of Safety And Effectiveness In Medical Device Software.
- Overview Of IEC 62304 Standard For Regulatory Compliance.
- Integrating IEC 62304 Into Medical Device Software Development Processes.
- Current Best Practices For Achieving IEC 62304 Compliance.
- Practical Strategies For Identifying And Mitigating Cybersecurity Risks.
- Protecting Patient Safety Through Robust Cybersecurity Protocols.
- Tools And Knowledge For Resilient And ….
-
- Importance Of Safety And Effectiveness In Medical Device Software.
- Overview Of IEC 62304 Standard For Regulatory Compliance.
- Integrating IEC 62304 Into Medical Device Software Development Processes.
- Current Best Practices For Achieving IEC 62304 Compliance.
- Practical Strategies For Identifying And Mitigating Cybersecurity Risks.
- Protecting Patient Safety Through Robust Cybersecurity Protocols.
- Tools And Knowledge For Resilient And Compliant Software Development.
Course Description
Stay ahead of the latest cybersecurity threats facing medical device software with our 90-minute webinar.
Discover proven strategies and industry best practices to prevent and mitigate risks, ensuring compliance with IEC 62304 and safeguarding patient safety.
Cybersecurity is critical for the safety and effectiveness of medical devices. Without robust protections, software vulnerabilities can lead to severe injuries or even fatalities. Learn how to fortify your devices against these risks.
Key Learning Points:
-
- Insight into emerging cybersecurity threats impacting medical device software in 2024.
- Practical methods for implementing industry-standard security practices, including physical and logical protections.
- How to achieve and maintain compliance with IEC 62304 standards.
- Strategies for mitigating vulnerabilities to protect patient data and device functionality.
This webinar is perfect for regulatory professionals, software developers, and compliance managers in the medical device industry looking to enhance cybersecurity and stay compliant with evolving standards.
What You Will Gain:
-
- A clear understanding of current cybersecurity challenges and how to address them.
- Practical tips for integrating IEC 62304 guidelines into your security protocols.
- Confidence in implementing best practices that ensure device safety and regulatory compliance.
Join us to ensure your medical devices remain secure, compliant, and ready for 2024-25’s challenges.
Stay ahead of the latest cybersecurity threats facing medical device software with our 90-minute webinar.
Discover proven strategies and industry best practices to prevent and mitigate risks, ensuring compliance with IEC 62304 and safeguarding patient safety.
Cybersecurity is critical for the safety and effectiveness of medical devices. Without robust protections, software vulnerabilities can lead to severe injuries or even fatalities. Learn how to fortify your devices against these risks.
Key Learning Points:
-
- Insight into emerging cybersecurity threats impacting medical device software in 2024.
- Practical methods for implementing industry-standard security practices, including physical and logical protections.
- How to achieve and maintain compliance with IEC 62304 standards.
- Strategies for mitigating vulnerabilities to protect patient data and device functionality.
This webinar is perfect for regulatory professionals, software developers, and compliance managers in the medical device industry looking to enhance cybersecurity and stay compliant with evolving standards.
What You Will Gain:
-
- A clear understanding of current cybersecurity challenges and how to address them.
- Practical tips for integrating IEC 62304 guidelines into your security protocols.
- Confidence in implementing best practices that ensure device safety and regulatory compliance.
Join us to ensure your medical devices remain secure, compliant, and ready for 2024-25’s challenges.
Why you should attend
Ensuring the safety and effectiveness of medical devices is a priority for everyone involved in their development, manufacturing, testing, and distribution.
With cybersecurity threats becoming more frequent and sophisticated, staying ahead is no longer optional—it’s essential.
Top Reasons to Attend This Webinar:
-
- Protect Patient Safety: Learn how cyberattacks can compromise device functionality and how to implement proven strategies to safeguard patient data and safety.
- Stay Compliant with IEC 62304: Gain insights into the latest industry standards and ensure your organization remains compliant with IEC 62304 requirements.
- Proactively Identify and Mitigate Risks: Understand how to identify emerging threats before they cause damage, and learn practical methods to neutralize risks before they impact your devices.
- Stay Competitive in a Growing Field: Enhance your expertise in medical device cybersecurity, making you a more valuable asset in a field where regulatory scrutiny and security demands are increasing.
- Actionable Best Practices: Discover industry best practices for integrating cybersecurity protocols into your product lifecycle, enabling you to lead your team in adopting cutting-edge protections.
This training will equip you with the knowledge and skills needed to tackle today’s cybersecurity challenges—ensuring your medical devices remain secure, regulatory-compliant, and ready for 2024’s evolving landscape.
Don’t miss this opportunity to stay ahead in the field and secure your organization’s future.
Register now!
Ensuring the safety and effectiveness of medical devices is a priority for everyone involved in their development, manufacturing, testing, and distribution.
With cybersecurity threats becoming more frequent and sophisticated, staying ahead is no longer optional—it’s essential.
Top Reasons to Attend This Webinar:
-
- Protect Patient Safety: Learn how cyberattacks can compromise device functionality and how to implement proven strategies to safeguard patient data and safety.
- Stay Compliant with IEC 62304: Gain insights into the latest industry standards and ensure your organization remains compliant with IEC 62304 requirements.
- Proactively Identify and Mitigate Risks: Understand how to identify emerging threats before they cause damage, and learn practical methods to neutralize risks before they impact your devices.
- Stay Competitive in a Growing Field: Enhance your expertise in medical device cybersecurity, making you a more valuable asset in a field where regulatory scrutiny and security demands are increasing.
- Actionable Best Practices: Discover industry best practices for integrating cybersecurity protocols into your product lifecycle, enabling you to lead your team in adopting cutting-edge protections.
This training will equip you with the knowledge and skills needed to tackle today’s cybersecurity challenges—ensuring your medical devices remain secure, regulatory-compliant, and ready for 2024’s evolving landscape.
Don’t miss this opportunity to stay ahead in the field and secure your organization’s future.
Register now!
Areas Covered
-
- Understanding the Importance of Safety and Effectiveness
Discover why ensuring safe and effective medical devices is crucial for everyone involved in software development and the broader medical device industry. - Overview of IEC 62304 Standard
Gain a clear understanding of the IEC 62304 standard and how it applies to medical device software, ensuring you stay up-to-date with regulatory requirements. - Applying IEC 62304 to Your Processes
Learn how to integrate IEC 62304 into your workflows, with step-by-step guidance on aligning software development processes with the standard’s requirements. - Industry Best Practices for Compliance
Explore current best practices that can streamline compliance with IEC 62304, helping your organization adopt proven methods to enhance cybersecurity and software quality. - Practical Tips for Improving Cybersecurity in Medical Devices
Understand practical strategies for identifying vulnerabilities, mitigating risks, and protecting patient safety through robust cybersecurity protocols.
- Understanding the Importance of Safety and Effectiveness
BONUS:
-
- PDF copy of the presentation handout for your future reference.
- Soft copy of the certificate of completion on request.
- Q&A Session with the Presenter: Get your pressing questions answered verbally, via chat or email
-
- Understanding the Importance of Safety and Effectiveness
Discover why ensuring safe and effective medical devices is crucial for everyone involved in software development and the broader medical device industry. - Overview of IEC 62304 Standard
Gain a clear understanding of the IEC 62304 standard and how it applies to medical device software, ensuring you stay up-to-date with regulatory requirements. - Applying IEC 62304 to Your Processes
Learn how to integrate IEC 62304 into your workflows, with step-by-step guidance on aligning software development processes with the standard’s requirements. - Industry Best Practices for Compliance
Explore current best practices that can streamline compliance with IEC 62304, helping your organization adopt proven methods to enhance cybersecurity and software quality. - Practical Tips for Improving Cybersecurity in Medical Devices
Understand practical strategies for identifying vulnerabilities, mitigating risks, and protecting patient safety through robust cybersecurity protocols.
- Understanding the Importance of Safety and Effectiveness
BONUS:
-
- PDF copy of the presentation handout for your future reference.
- Soft copy of the certificate of completion on request.
- Q&A Session with the Presenter: Get your pressing questions answered verbally, via chat or email
Who is this course for
Everybody benefits from watching this. Even better when done as a group!
-
- Regulatory Affairs Managers Seeking To Ensure Compliance
Understand how to align medical device software with IEC 62304 to meet regulatory standards and avoid compliance issues. - Quality Assurance Professionals Focused On Enhancing Software Safety
Gain insights into cybersecurity best practices to ensure device reliability and patient safety. - Software Developers Looking To Integrate Security Protocols
Learn how to apply IEC 62304 guidelines into daily development processes for safer software solutions. - Product Managers Aiming To Minimize Product Risk
Understand potential cyber threats and implement strategies that protect device functionality and market reputation. - Cybersecurity Specialists Working To Prevent Device Vulnerabilities
Discover practical methods to identify and address security gaps in medical device software. - Compliance Officers Looking To Stay Ahead Of Evolving Standards
Stay informed about current industry trends and best practices to maintain regulatory compliance. - Medical Device Manufacturers Focused On Delivering Safer Products
Learn how cybersecurity measures can be integrated into device lifecycle to ensure safe product launches. - Operations Managers Seeking To Enhance Team Training On Cybersecurity
Equip your team with the knowledge to identify threats and mitigate risks effectively. - Healthcare Technology Innovators Aiming For Long-Term Security
Explore cutting-edge strategies for protecting device software and maintaining trust with patients and stakeholders.
- Regulatory Affairs Managers Seeking To Ensure Compliance
Everybody benefits from watching this. Even better when done as a group!
-
- Regulatory Affairs Managers Seeking To Ensure Compliance
Understand how to align medical device software with IEC 62304 to meet regulatory standards and avoid compliance issues. - Quality Assurance Professionals Focused On Enhancing Software Safety
Gain insights into cybersecurity best practices to ensure device reliability and patient safety. - Software Developers Looking To Integrate Security Protocols
Learn how to apply IEC 62304 guidelines into daily development processes for safer software solutions. - Product Managers Aiming To Minimize Product Risk
Understand potential cyber threats and implement strategies that protect device functionality and market reputation. - Cybersecurity Specialists Working To Prevent Device Vulnerabilities
Discover practical methods to identify and address security gaps in medical device software. - Compliance Officers Looking To Stay Ahead Of Evolving Standards
Stay informed about current industry trends and best practices to maintain regulatory compliance. - Medical Device Manufacturers Focused On Delivering Safer Products
Learn how cybersecurity measures can be integrated into device lifecycle to ensure safe product launches. - Operations Managers Seeking To Enhance Team Training On Cybersecurity
Equip your team with the knowledge to identify threats and mitigate risks effectively. - Healthcare Technology Innovators Aiming For Long-Term Security
Explore cutting-edge strategies for protecting device software and maintaining trust with patients and stakeholders.
- Regulatory Affairs Managers Seeking To Ensure Compliance
Instructor Profile
Carolyn (McKillop) Troiano has more than 40 years of experience in the tobacco, pharmaceutical, medical device and other FDA-regulated industries. She has worked directly, or on a consulting basis, for many of the larger pharmaceutical and tobacco companies in the US and Europe, developing and executing compliance strategies and programs. Carolyn is currently active in the Association of Information Technology Professionals (AITP), and Project Management Institute (PMI) chapters in the Richmond, VA area.
During her career, Carolyn worked directly, or on a consulting basis, for many of the larger pharmaceutical companies in the US and Europe. She developed validation programs and strategies back in the mid-1980s, when the first FDA guidebook was published on the subject, and collaborated with FDA and other industry representatives on 21 CFR Part 11, the FDA’s electronic record/electronic signature regulation.
