Roadmap to Compliance - Bench to Bedside
Medical technologies are proven to have a positive impact on our health, from prevention, diagnosis, treatment and beyond. The world has changed so dramatically over the last few years to such a degree that global healthcare demands for innovation, resilience and value are at their highest ever seen. This has created opportunities and challenges for patients, healthcare providers, regulators, investors and manufacturers alike. These include the surging demand for advanced diagnostics, the power of software and digital health, and medical technology shortages due to regulatory changes and supply chain issues. They are changing the entire paradigm of how and where healthcare is delivered as well as regulated.
Element's MedTech Conference seeks to challenge the existing regulatory structures and discuss how medical technologies can be brought into play at the right time and within a framework that optimises time to market and delivers a higher degree of confidence that those technologies will positively impact health outcomes, healthcare costs and environmental and societal impact.
The event forms part of a range of planned educational and digital navigational tools to be delivered through Element’s Global MedTech Academy to support faster access to the market of innovative and safer medical technologies.
Our agenda takes the audience from the funding innovation landscape, regulatory pathways, approaches to testing (in vivo, in vitro, and in silico), and beyond compliance.
This free event will support you in navigating the regulations to bring your concept from 'bench to bedside' using some of the latest testing methods and strategies for compliance.
Who should attend:
What can I learn?
During the conference, our speakers will discuss:
- MedTech Industry Landscape
- Innovation Landscape & Funding for Regulatory Support
- Navigating Regulatory Pathways
- Approaches to R&D Compliance Testing
- Beyond Compliance
- Enhanced by a dynamic Q&A and polls to answer your questions
Speakers include:
- Ashleigh Batchen, Regulatory Affairs Manager, BIVDA
- Phil Brown, Director, Regulatory & Compliance, ABHI
- Eammon Hoxey, Director, E V Hoxey Ltd
- John Wilkinson, MedTech Vision Consultant and Chair of GMDN
- Professor Michael Lewis, Life Science and Innovation, University of Birmingham and Joint Director, NIHR
- Lewis Oakley, Innovation Lead - Heath Technologies, Innovate UK
And also, Element’s technical and regulatory subject matter experts include Maria Artiles, Harvey Stubbs, Paul Batchelder, Nicole Small, James Pink and Michael Kipping.
This conference represents a unique opportunity for learning and expanding networks enabled by live presentations, panel discussions, and dynamic Q&A sessions with polls (slido) as well as access to post-event content.
If you can't attend the event in person, click here to register for the online event.
Event details
Date: March 22, 2023
Time: 09:00 am - 04:00 pm (GMT)
Location: The Manufacturing Technology Center (MTC), Ansty Park, Coventry, CV7 9JU
Register Now
Register for the MedTech Academy at the Manufacturing Technology Centre in Coventry.
Related Services
Medical Device
As a comprehensive testing partner, you’ll enjoy the benefit of a single supplier source for all of your testing needs, from mechanical testing and environmental simulation to EMC and wireless device testing.
Medical Device Regulatory Services
Element’s regulatory advisors have 30 years of domestic and international regulatory consulting experience, specializing in handling the most complex challenges and partnering with you on the path to submission.
Medical Device Radio Testing
Our medical regulatory affairs experts can identify the appropriate Radio Testing standards and certification, helping to remove both the cost and risk from medical product verification and validation during the formal testing phase.
Medical Device Testing Tips
Preparing for a medical device testing program can be a challenge for many manufacturers, especially if it is a new or novel product or if time is limited. Our medical device experts share their testing tips and best practices.