Balancing Risks, Compliance, and Innovation in Medical Device Development

What you can learn:

Developers of medical devices and other medical technology are in a difficult spot. Not only are they operating at the cutting edge of technology innovation, an inherently risky business. But they must also meet regulatory compliance requirements of various local or international standards. To top it off, they have to juggle those aspects while outpacing competitors in order to stay profitable.

Watch this Experts Talk webinar with Intland Software’s Functional Safety expert and Quality Consultant Szabolcs Agai. In this webinar, Intland’s expert provides insights on striking that delicate balance between fast innovation, adequate risk management, and stress-free regulatory compliance.

Intland Software’s expert shares practices to improve your teams’ performance in the delivery of advanced medical technology. In this webinar, we also demonstrate how Intland’s Medical Software Engineering Template helps you tackle risks, accelerate product development, and simplify compliance audits.

• Implementing a risk-focused, fully compliant medical device innovation process
• Integrating quality, product development, and regulatory compliance aspects in medtech delivery
• Identifying, analyzing, reporting on, and managing risks and hazards in compliance with ISO 14971
• Best practices of medtech lifecycle management based on our expert’s field experience

Our webinar is intended for:

Project Managers and Team Leaders, Product Quality and Test Engineers, Heads of Testing & QA teams, Embedded Software Developers, Business Analysts, Regulatory Compliance Analysts