Top Medical Device Contract Manufacturing Manufacturers in Germany

Medical Device Partners is dedicated to fostering long-term relationships in the medical devices industry, providing guidance to suppliers and manufacturers looking to enter or expand in this sector. With a strong presence in Europe and a commitment to reliability, they represent a wide range of medical products and services.

Maxcert specializes in regulatory and quality consulting for medical device manufacturers, offering expertise to navigate the complexities of compliance and registration in the EU and UK markets. Their services include EU representation, technical file evaluation, and support for product commercialization, making them a valuable partner for those developing and introducing medical devices.

Meotec GmbH specializes in contract manufacturing within the medical technology field, focusing on innovative technologies and high-quality execution. Their expertise includes the production of sophisticated products and implant system development, making them a reliable partner for medical device manufacturing.

Anteris Medical specializes in the development of drug/device combination products, offering strong project management, regulatory affairs, and quality consulting, particularly for autoinjectors, pens, and needle-safety devices. Their expertise in medical device development and compliance with ISO 13485 and 21 CFR 820 ensures effective management throughout the product lifecycle.

NEXTEC specializes in medical device contract manufacturing, offering comprehensive services that include design, development, and distribution under MDR and IVDR regulations. With over 25 years of experience, they act as a Legal Manufacturer and European Authorised Representative, ensuring compliance and supporting the entire software lifecycle process for medical device software development.

MT Promedt Consulting assists medical device manufacturers globally with the approval and clearance process, international product registration, and the development of quality management systems, ensuring compliance with European Medical Device Regulations. Their expertise as a European Authorized Representative and strategic regulatory consulting can be invaluable for those in the medical device contract manufacturing sector.

TRIQ is a full-service Clinical Research Consultancy Group with extensive experience in conducting medical device clinical trials across various therapeutic areas, including cardiovascular and neurology, in accordance with EU regulations. They offer a comprehensive range of clinical research services, providing a streamlined approach for medical device development and support, particularly beneficial for start-ups and smaller companies.

Integer is a global leader in medical device contract manufacturing, offering advanced design and production capabilities for a variety of medical technologies. Their expertise in collaboration with leading OEMs ensures innovative solutions that enhance patient care.

Mars Medical, located in Germany's leading medical device development region, offers consultation and representation services for medical devices in the EU. They provide support for product registration, clinical investigations, and quality management system setup, making them a valuable partner for manufacturers looking to navigate the European market.

The company offers specialized regulatory consulting services for medical device manufacturers, including support for device registrations, quality management, and compliance with EU regulations and MDSAP standards. Their expertise encompasses biological and clinical evaluations, performance assessments, and comprehensive quality management, making them a valuable partner for complex projects in medical technology.