Join us in Frankfurt to hear from a host of expert speakers and innovators who will enable you to accelerate your own software development journey. Whether you’re working directly in software development, or in QA, RA, or cybersecurity, this is the event for you

Download the 2022 conference brochure to explore the key themes being discussed at this year's event from leading experts such as: 

• John Mulcahy, CEO, HealthGenuity & VP Product, S3ConnectedHealth
• Jan Van Moll, Advanced Development Global Lead for Quality & Regulatory, Philips
• Harsh Jain, Quality Manager, Align Technology
• Celestina Bianco, Quality Assurance and Regulation Affair Director, Werfen
• Ehab Shakour, CTO & IP Director, InnoSphere
  

Medical devices are becoming increasingly complex with rapid advancements of their software and Artificial Intelligence (AI) acting as a smarter ‘brain’ behind their hardware. The advancements of medical device software and a new clause from the Medical Device Regulation (MDR) has seen the industry face increased regulatory scrutiny and caused unique challenges such as, different regulatory demands across countries, ever-changing guidelines and a lack of consensus between manufacturers. In the face of such challenges, compliance and quality assurance of medical device software is more important now than ever before.

Ahead of this year's Software Design for Medical Devices event, this infographic explores the current compliance and regulatory issues facing medical device software and provides solutions to help industry professionals maintain regulatory compliance.

Download the full infographic now >>

In February 2020, we’re taking our innovative focus to the next level to ensure your teams can best achieve regulatory compliance, are protected from cyber threats and are implementing agile methodology into your software, all while embracing cutting edge designs to get your product to market faster and staying ahead of your competition.

In light of this rapidly evolving landscape of software development for medical devices, Pharma IQ has created a post-show report highlighting the most exciting takeaways from last year’s event.

Download the full report on the right >>

Other key benefits to downloading the full report:

• An overview of bullet-proofing the security of your device against increasing levels of cyber threat during the digital transformation of healthcare
• An understanding to ensure regulatory compliance across the globe with effective documentation and a deep understanding of EU and US regulations