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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

MedTech Summit

12-16 October 2020, Dublin

EU MDR & IVDR: 2 Years To Go. 2 Regulations To Meet. Are you ready?

Biocompatibility for Medical Devices

15-16 October 2020, Dublin

Thank you to all who made this year's event a huge success! Stay tuned for 2020 updates.

Biocompatibility for Medical Devices US

December 1 - 3, 2020, Philadelphia, PA

Navigate the evolving biocompatibility landscape for medical devices

MedTech Summit US

December 1-3, 2020, Philadelphia, PA

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

Training

Showing 4 of 24 coursesView all courses

Applying the Regulations for Health Apps and Medical Device Software

Starting 3 August 2020, 5 weeks online

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

Regulatory Affairs in Latin America for Medical Devices

23 - 24 September 2020, London

Develop your understanding of the regulatory Landscape in Latin America and learn to overcome common challenges to ensure fast device registration

Medical Device School

10 - 12 Nov 2020, London

Essential training for a thorough understanding of all processes from concept to post-market with focus on the new Medical Device Regulation

Customised Learning Solutions for the Life Sciences Industry

In-House | e-Learning | Blended

Accelerate your team with customised learning solutions in pharmaceuticals, biopharmaceuticals, medical devices and agriculture

Articles & Video

Showing 9 of 24 articles & videoView all articles & video
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.

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MDSAP

Preparing your organisation for MDSAP: Australia, Canada, Japan, Brazil - WHITEPAPER

This whitepaper details how your organisation can prepare for the Medical Device Single Audit Program (MDSAP) in Australia, Canada, Japan and Brazil.

Life Sciences

The biggest breakthroughs in life sciences the last 10 years

CRISPR, CAR-T, immunotherapies, genome sequencing, AI - what is the biggest breakthrough in the life sciences in the last 10 years?

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Diversity and Inclusion

Diversity in the life sciences workplace: Implementing a leading corporate culture for innovation - WHITEPAPER

This paper looks at how to foster racial, gender, geographical, neuro and cognitive diversity in the life sciences to achieve an inclusive culture built for innovation.

Diversity

REPORT: Diversity, Inclusion and Sustainability in the Global Life Sciences Industry 2020

EU MDR

MedTech Digital Week 2020 agenda revealed

COVID-19

The role of COVID-19 antibody testing for employers

Life Sciences

Looking to 2030 Report: The Future of the Global Life Sciences and Pharma Industry

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COVID-19

COVID-19 Report: The Response to and Impacts on the Global Life Sciences Industry

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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