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Regulatory Affairs, Medical Devices

Notified Body designation and scope, the impact of Brexit and Competent Authority and Notified Body interpretation of the regulations. Make sure you are up to date!

Events

Showing 4 of 5 eventsView all events

Biocompatibility for Medical Devices US

More details soon

Navigate the evolving biocompatibility landscape for medical devices

MedTech Digital Week

Explore The Latest EU MDR And IVDR Updates And Guidance With This Complimentary 3-Day Webcast Series

MedTech Summit US

DateTBC, Philadelphia, PA

THANK YOU TO EVERYONE WHO ATTENDED THE 2019 MEDTECH SUMMIT US!

MedTech Summit

12-16 October 2020, Now delivered as a 100% Virtual Conference in Central European Summer Time Zone (CEST)

EU MDR, IVDR & Global Market Regulations: Bringing The Latest Guidance To You

Training

Showing 4 of 22 coursesView all courses

Applying the Regulations for Health Apps and Medical Device Software

2021 Dates TBC, 5 weeks

Learn about Safety & Security Risk Management, Design Control, Clinical Evaluation and Usability Engineering for Health apps and Medical Device Software

Medical Device School

2021 Dates TBC, 3 days

Gain a practical overview of the processes involved in bringing a medical device to market led by an expert faculty

Successful Medical Device & IVD Post Market Surveillance and Vigilance Reporting

2021 Dates TBC, 2 days

Gain a practical understanding of IVD PMS and vigilance strategies under the MDR to ensure compliance

Fundamentals of the EU IVD Regulation

12 October 2020, 5 weeks

Decode the new European IVD regulation - understand the key areas of impact for IVDs within the new regulatory requirements

Articles & Video

Showing 9 of 32 articles & videoView all articles & video
Featured
MedTech eBook Series

The EU MDR Delay and Implementation - MedTech eBook Series

Discover the challenges of EU MDR implementation and impacts of the delay on the medical device industry in this MedTech eBook.

Premium
MedTech

MedTech Report 2020: EU MDR and IVDR Compliance

Download the MedTech Report 2020 on EU MDR and IVDR Compliance, based on 265 survey responses from industry insiders.

Survey

Survey: Adoption of AI and Digital Solutions in the MedTech Industry

Take part in our study to discover the adoption of AI and digital solutions in the MedTech industry.

MedTech eBook Series

Clinical Evaluations for Medical Devices and IVDs - MedTech eBook Series

Discover how the EU MDR will affect clinical evaluations for medical devices and IVDs in this MedTech Summit eBook.

COVID-19

Report: Partnering And Deal-Making in Pharma through the Pandemic

Healthcare

REPORT: The Future of Healthcare Post COVID-19

Diversity and Inclusion

Women in Pharma: 44% of pharma professionals think that women are under represented in their organization

Regulatory affairs

Barriers and Challenges for Global Regulatory Harmonization

Drug Development

Pharma R&D Annual Review 2020

SPONSORSHIP & EXHIBITION OPPORTUNITIES

Let us help you engage qualified decision makers in need of experts and services to ensure compliant medical device products. Share your strategy and plans so we can help you identify the best opportunities to reach your objectives. Our team will collaborate with you to develop a bespoke program tailored to your unique needs.

To find out more about sponsor opportunities, contact Linda Cole:
linda.cole@informa.com | +44 207 017 6631

Download Medtech Sponsor Prospectus

All opportunities can be customised to align with your needs and budget. Examples may include:

  • Exhibition space
  • Speaking slots and onsite video interviews
  • High-impact branding and messaging
  • Private/public hosted events (lunches, breakfasts, and receptions)
  • Custom digital campaigns

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