FDA Premarket and Postmarket Medical Device Cybersecurity

Navigating the complex FDA security requirements for medical devices can prove both time-consuming and costly. Organizations need a trusted advisor who can help expedite the pre-market submission process, enabling them to bring secure and effective devices to market faster.

Streamline your path to FDA pre-market approval. Download our white paper to arm yourself with the most relevant, up-to-date knowledge and strategies necessary to successfully navigate the FDA regulatory process.

Once in market, use this white paper to understand how to constantly monitor and protect your device from cyberattacks through activities such as Attack Surface Management, Continuous Red Teaming, and Managed Offensive Security.

What You’ll Get

In this white paper, discover how to:

• Take a proactive approach to expedite the FDA application and approval process
• Develop an enduring security strategy for the entire medical device lifecycle
• Manage ongoing cyber risks while consistently meeting regulatory requirements.
• Ensure ongoing safety through postmarket monitoring
• Build a tailored offensive security approach for continuous monitoring and protection from threats to your device