LS Academy

NETWORKING EVE EXPERIENCE

More than just a cocktail – an evening designed to connect, engage, and inspire.

Elevate your conference experience with an exclusive evening designed for meaningful connections.
Join industry peers and thought leaders from the medical devices field for a refined networking experience that blends conversation, atmosphere, and taste.

Enjoy a cocktail experience enriched with a chef-selected first course, a perfect combination of social atmosphere and dining experience.

Hosted at LiQuido Rooftop Bar, an urban oasis with breathtaking views over the Milan skyline.

Where: Liquido Rooftop Bar, Via Giovanni Battista Pirelli 5, Milan
When: Thursday, October 15th, 2026, from 6:30 PM

Registration for the cocktail is conditional on attendance at the conference.

Indietro

Registrati

Metodi di pagamento accettati: Bonifico bancario, Carta di credito, PayPal.

Versione Stampabile

Contattaci per ricevere maggiori informazioni sulle opportunità di sponsorizzazione

Diventa Sponsor

Media Partner

Patrocinio

Code of Good Conduct - 270kB

<p style="text-align: center;"><strong>NH Collection Milano Touring<br />
</strong>Via Ugo Tarchetti 2 – 20121 Milan</p>

NH Collection Milano Touring
Via Ugo Tarchetti 2 – 20121 Milan

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MedDev Day

FAQ – Frequently Asked Questions

Is MedDev Day held annually?

Yes. MedDev Day is an annual medical device conference held each autumn in Europe. Each edition focuses on current developments in medical device regulation, EU MDR and IVDR implementation, notified body requirements, and regulatory affairs strategy relevant to the European medical device community.

What is the difference between individual edition pages and this main page?

This page provides an overview of MedDev Day as an annual medical device conference series, covering its history, recurring themes, and professional community. Individual edition pages offer specific details about that year’s programme, speakers, registration, and focused topics. This main page serves as the canonical reference for the overall MedDev Day conference series.

Who should attend MedDev Day?

The medical device conference is designed for regulatory affairs professionals, quality management specialists, clinical affairs teams, medical affairs personnel, post-market surveillance experts, notified body staff, and anyone responsible for medical device regulation compliance in medical device manufacturers, CROs, or regulatory agencies.

How does MedDev Day address both MDR and IVDR?

MedDev Day provides comprehensive coverage of both EU MDR and IVDR frameworks. Sessions address medical device-specific requirements, in vitro diagnostic requirements, and shared elements like quality management systems, clinical evidence, and post-market surveillance. The conference recognizes that many medical device companies work with both regulations and require integrated regulatory affairs strategies.

Will notified bodies participate in MedDev Day?

Yes. MedDev Day regularly features presentations and panel participation from notified body representatives. These sessions provide direct insight into conformity assessment expectations, technical documentation review processes, and quality system audit requirements under EU medical device regulation. Notified body participation ensures medical device manufacturers understand current assessment practices and can optimize their conformity assessment strategies.

How can I stay informed about upcoming MedDev Day editions?

Subscribe to the LS Academy newsletter or follow our updates to receive announcements about MedDev Day editions, including programme details, speaker confirmations, and early registration opportunities for this leading medical device conference.

What makes MedDev Day different from other medical device regulation conferences?

MedDev Day specifically addresses the European medical device regulation landscape with practical, operations-focused content. The medical device conference brings together multi-stakeholder perspectives (manufacturers, notified bodies, regulators) and emphasizes EU MDR and IVDR implementation, notified body requirements, and real-world regulatory affairs challenges rather than theoretical discussions. Its focus on EU Single Market opportunities and regulatory efficiency reforms distinguishes it from general medical device conferences.

Ordinaria Acquistabile fino al 14/10/2026	€790,00
Freelance - Privato - Accademia - Pubblica Amministrazione Acquistabile fino al 14/10/2026	€480,00
Networking Cocktail Experience Acquistabile fino al 09/10/2026	€45,00

Conferenza

MedDev Day - Networking Eve Experience

Building Opportunities in the EU Single Market
Clearer rules. Smarter pathways. Stronger innovation.

15 and 16 October 2026

Milan

Attestato di partecipazione

Registrati

Sponsors

Media Partner

Patrocinio

FAQ – Frequently Asked Questions

Is MedDev Day held annually?

What is the difference between individual edition pages and this main page?

Who should attend MedDev Day?

How does MedDev Day address both MDR and IVDR?

Will notified bodies participate in MedDev Day?

How can I stay informed about upcoming MedDev Day editions?

What makes MedDev Day different from other medical device regulation conferences?

Stay Connected with MedDev Day