MOA Berlin,
Berlin, Germany
ACCESS MEDICAL DEVICE AND IVD MARKETS AT THE FLAGSHIP REGULATORY EVENT OF THE YEAR
Save Time, Effort, and Money While Ensuring Compliance with Global Regulations, and Engaging with the EU Commission, Notified Bodies, Competent Authorities, Working Groups, and Manufacturers
Gain Comprehensive Insights for Medical Device and IVD Manufacturing. 8 Vital Topics: EU MDR, IVDR, Clinical Evaluations & Investigations, Performance Evaluations, Post-Market Surveillance, Software & AI/ ML, Biocompatibility, Law & Compliance, and Global Market Access
MedTech Summit 2024 Hybrid Agenda At A Glance
Take a look at the full MedTech Summit 2024 agenda at a glance to see how you and your team can benefit!
As a hybrid event, delegates will have the option to attend either in-person or digitally.
All in-person presentations taking place in Brussels will be recorded and made available on-demand for 10 working days on our ConnectMe platform, and then for up to 12 months on our Streamly platform, for you to watch at a time that suits you.
Maximise your MedTech Summit experience with our Core Training Course and a two power-packed Workshop Sessions
IVD Workshop: Compiling and Completing Technical Documentation
- Structure technical documentation files effectively
- Understand Notified Body code assignments
- Ensure data meets regulatory requirements
- Curate and execute performance evaluations
- Harvest and analyse relevant clinical evidence
- Continue compliance through effective post-market surveillance
Biocompatibility Workshop: Biological Evaluation Execution & Authorship
- End to end process of biological evaluation plans
- Foundations of biological evaluations
- Test design for BEP
- Determining endpoint tests and critical factors
- Interpreting test results for analysis
- Transitioning data into BER
- Incorporating toxicology
- Lifecycle management of biological evaluation
Training Course: Medical Device Regulatory Project Management
- Early stage development of regulatory strategies
- Establishing a project team
- Establishing and monitoring standards for the entire device lifecycle
- Incorporating clinical evaluations
- Implementing risk management
- Understanding metrics used for project management and NB performance
- Adapting procedures as the lifecycle develops
Who Could You Be Joining at MedTech 2025
20+
Competent Authority & Notified Body Speakers
400+
Leading MedTech Industry Stakeholders
120+
Medical Device, IVD, SaMD, Combination Product and Legal Companies Represented
CONNECT WITH KEY DECISION MAKERS AT MEDTECH SUMMIT 2025
Whether you're increasing your company profile, launching a new product or creating business development opportunities, we have a package to suit your needs.
We can provide flexible and tailored solutions to optimise your investment.
For information on how your organisation could benefit from this hybrid event and to discuss the full range of lead generating, networking and branding opportunities, please contact:
Neha Singh
Email: NSingh@informaconnectls.com
