Our Expertise – Your Advantage
International Experience in the Medical Device Industry – Trusted Partnerships Worldwide
Count on Us for National and International Regulatory Approvals
Why Choose Us?
• Tailored to Your Needs:
Our Approach Is Specifically Designed for Your Requirements
• Clear and Structured:
Our Form Templates Ensure Simple and Transparent Documentation
• Efficiency That Pays Off:
We Reduce Your Effort so You Can Focus on Growing Your Business
Trust Us – Focus on Your Market While We Take Care of Product Surveillance!
Contact Us to Schedule an Appointment or Receive Expert Advice:
📞 +49(0) 170-260-52-47
MDR Made Simple – With CJ Management Service
Quality Management Consulting:
We provide support in implementing and optimizing quality management systems in compliance with international standards and regulations.
Global Product Approval:
We provide consulting and support in meeting regulatory requirements to ensure the smooth market entry of your products – whether in Europe, the USA, Brazil, Canada, Asia, or other regions.
Project Support and Process Optimization:
From product development to regulatory approval and the continuous optimization of business processes – we support you with tailored strategies and solutions.
EU Authorized Representative for Non-EU Manufacturers:
We provide legal representation, registration, communication with notified bodies, and support in case of recalls. With our comprehensive service, we stand by your side every step of the way.
