As a globally recognized testing and certification center for medical devices with accredited laboratories across Europe, North America, and Asia, Applus+ Laboratories can't wait to participate in MEDICA 2025, the premier international event for the medical technology sector.
Do you want to explore how we can support medical device manufacturers in bringing safe, effective, and compliant products to market worldwide? Then come and connect with us at MEDICA 2025, where we'll be waiting for you to hear your vision and help turn it into certified reality!
We offer a comprehensive portfolio of testing and certification services tailored to the medical device industry, helping manufacturers meet global regulatory requirements and ensure product safety and performance.
Our services include:
Our laboratories are accredited to support regulatory pathways in key markets such as the FDA (USA) and NMPA (China). In Europe, we provide full support through our two Notified Bodies (NB 2764 and NB 3121) under the Medical Device Regulation 2017/745 (MDR).
We are also accredited under ISO/IEC 17021-1 to certify Quality Management Systems in accordance with ISO 13485, ensuring compliance and excellence across the medical device lifecycle.
We combine technical expertise with global reach. Our integrated approach, from testing to certification, enables faster innovation, smoother MDR transitions, and enhanced patient safety. Rely on a trusted partner who brings precision, efficiency, and regulatory insight to every step of your product journey.
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