Applus+ Laboratories participates at the 14th edition of La Rentrée du DM
Applus+ Laboratories participates at the 14th edition of La Rentrée du DM 2026, one of France’s leading conferences dedicated to the medical device industry. As your global partner for testing and certification, supporting your market access journey, Applus+ Laboratories will present at booth 20 its full medical device offering, combining Notified Body services, ISO 13485 certification, and testing capabilities to support manufacturers across the product lifecycle and regulatory pathway.
- Start date: 06/10/2026
- End date: 07/10/2026
- City: Kursaal Congress Centre, Besançon
- Country: France
- Event Website: https://www.larentreedudm.com/
Discover our complete testing, certification and market access portfolio for medical devices
Visit our booth number 20 to learn how Applus+ Laboratories supports medical device manufacturers throughout the entire product lifecycle, from development and validation to certification, regulatory pathway planning, market access, and post-market activities. By visiting us, you will:
- Discover a comprehensive range of testing, certification, and conformity assessment services for medical devices.
- Discuss your challenges with our experts accross technical, regulatory, packaging, materials, performance, Notified Body, or ISO 13485 certification.
- Understand how Applus+ Laboratories can support your MDR pathway and international market access requirements through testing, certification, and conformity assessment services.
- Explore solutions that help accelerate product development while reducing technical and regulatory risks.
- Gain insights into evolving industry trends and regulatory expectations.
In addition to testing and validation, Applus+ Laboratories provides certification and conformity assessment services for medical devices, including Notified Body services under the European MDR and ISO 13485 certification. This integrated scope enables manufacturers to address technical evidence, quality management system requirements, and regulatory expectations within a coordinated market access strategy.
Our areas of expertise
- Materials and chemical characterization: materials selection, failure analysis, chemical testing, extractables & leachables, and analytical investigations.
- Biocompatibility and biological evaluation: testing strategies and support aligned with ISO 10993 requirements for medical devices.
- Mechanical and functional testing: performance, durability, fatigue, wear, and biomechanical testing to demonstrate safety and reliability.
- Sterile barrier and packaging validation: packaging integrity, accelerated ageing, transport simulation, shelf-life studies, and packaging validation according to international standards.
- Regulatory and technical expertise: support for MDR pathway planning, technical documentation, risk management, change control, supplier changes, product development, and international market access strategy.
- Certification and conformity assessment: notified body services for European MDR requirements, ISO 13485 certification, quality management system assessment, and conformity assessment support for medical device market access.
- Electrical safety, EMC and cybersecurity: evaluation of connected and active medical devices to ensure compliance with applicable regulatory and technical requirements.
Meet our experts at La Rentrée du DM
Whether you’re developing an innovative medical device, validating a design change, evaluating a new supplier, preparing for certification, or planning a market launch, our team will be available to discuss the most appropriate strategy for testing, certification, and the regulatory process for your project.
Book a meeting with our team in advance to make the most of your visit.
Applus+ Laboratories: your partner for medical devices testing and certification
Applus+ Laboratories is your global partner for testing and certification, supporting your market access journey. We look forward to welcoming you at La Rentrée du DM 2026 and discussing how our notified body services, ISO 13485 certification, and testing capabilities can support your medical device strategy from development to market access and throughout the product lifecycle.
Can't attend the event? Contact our experts or request a quote.