Applus+ Laboratories will participate in La Rentrée du DM 2025
La Rentrée du DM is a leading French conference dedicated to medical devices, bringing together manufacturers, laboratories, consultants, regulatory authorities, and other stakeholders in the sector. This two-day event features sessions on regulatory updates, clinical issues, and best practices in the field.
- Start date: 07/10/2025
- End date: 08/10/2025
- City: Besançon
- Country: France
- Event Website: https://www.larentreedudm.com/
What you will discover at our booth
| Topic | Details |
| Validation & Characterization | Methods and approaches we use to ensure that medical devices meet physical, chemical, mechanical, and material performance standards. |
| Regulatory compliance (MDR / FDA / guidance from Notified Bodies) | Expert support to guide you through the complex regulations of MDR, FDA, NMPA, and Notified Bodies. |
| Regulatory expertise and support | From process design to market launch: regulatory strategy, risk assessment, technical file preparation, and audit support. |
Why meet us?
Applus+ Laboratories is your one-stop partner for medical device testing and certification. By visiting our booth, you will discover how we support companies worldwide with a full range of services, including:
- Biomechanical testing
- Chemical testing
- Packaging testing
- Safety and essential performance evaluations
- MDR regulatory compliance assessments
- Cybersecurity evaluations
Our mission is to help you ensure compliance, quality, and reliability at every stage of your medical device lifecycle through testing and certification services.
As a designated Notified Body under the EU MDR, Applus+ Laboratories provides accredited conformity assessment services and expert support to help manufacturers meet enhanced regulatory requirements and secure access to the European market.
Book a meeting with any of our experts in advance!
Meet us onsite!
Take advantage of this opportunity to:
- Discover our tailored solutions for your medical devices
- Discuss your specific technical or regulatory challenges
- Anticipate upcoming regulatory changes and their impact on market access
We look forward to welcoming you at Booth nº20 to discuss your medical device regulatory and validation needs.
Can’t attend La Rentrée du DM this year? Contact us directly or request a quote today!