CRM substances, nanomaterials and other ctitical substances in medical devices
Manufactured by
Hamburg, Germany
Ramboll is a global engineering, architecture and consultancy company with more than 18,000 experts that create sustainable solutions across energy, real estate, transport, water, waste, industry, finance, technology, healthcare and public sectors. Ramboll combines deep scientific expertise and technical acumen with a broad global footprint to deliver sustainable solutions helping our clients around the world to address some of the most challenging environmental and human health issues. Reputation for technical and scientific excellence, innovation and client service Deep scientific expertise and technical acumen Private and public sector clients around the world Extensive experience in the Americas, Europe, Africa and Asia Pacific Our services for medical device manufacturers include: international market access strategies; globally compliant quality management systems; MD (EU) 2017/745 and IVDR (EU) 2017/246 compliance services; risk management according to ISO 14971; biocompitability in line with ISO 10993; expert advice on dealing with critical substances; clinical evaluation and literature research; qualification and validation. Visit us at the joint stand of Innovative health technology Rhineland-Palatinate MEDICA 2025 – Stand E92/ Hall 3 .
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EPnP Medical GmbH · Germany
Advanced materials development and analysis for biocompatibility, sterilization compatibility, and long-term performance.
Maven Profcon Services LLP · India
Regulatory consulting services for CE marking of medical device software (SaMD) and in vitro diagnostics. Provides technical documentation preparation, clinical evaluation, risk management, and conformity assessment support to meet EU MDR requirements.
NMI Naturwissenschaftliches und Medizinisches Institut an der Universität Tübingen · Germany
Comprehensive biological assessment services for medical devices, including biocompatibility testing, material evaluation, and regulatory compliance support. NMI provides accredited testing and technical consulting at the interface of biomaterials and biological sciences to support device development and market approval.
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