EU MDR, IVDR and Global Market Regulations: Bringing The Latest Guidance To You
Biocompatibility for Medical Devices
Thank you to all who made this year's event a huge success! Stay tuned for 2020 updates.
Biocompatibility for Medical Devices US
Navigate the evolving biocompatibility landscape for medical devices
Customised Learning Solutions for the Life Sciences Industry
Accelerate your team with customised learning solutions in pharmaceuticals, biopharmaceuticals, medical devices and agriculture
Regulatory Affairs in Latin America for Medical Devices
Develop your understanding of the regulatory landscape in Latin America to ensure fast device registration
Applying the Regulations for Health Apps and Medical Device Software
Learn about Safety & Security Risk Management, Design Control, Clinical Evaluation and Usability Engineering for Health apps and Medical Device Software
Medical Device Regulatory Project Management
Learn how to apply project management skills to implement medical device regulatory changes and maintain compliance
Articles & Video
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.
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.
Women in Pharma: 44% of pharma professionals think that women are under represented in their organization
44% of pharma professionals think that women are under represented in their organization according to new data from an Informa Connect Life Sciences study. Here we deep dive into the data.
Pharma R&D Annual Review 2020Life Sciences
The biggest breakthroughs in life sciences the last 10 years
Diversity in the life sciences workplace: Implementing a leading corporate culture for innovation - WHITEPAPERDiversity
REPORT: Diversity, Inclusion and Sustainability in the Global Life Sciences Industry 2020EU MDR
MedTech Digital Week 2020 agenda revealed
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:
email@example.com | +44 207 017 6631
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