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About Us

  Beijing Regis Success Medical Tech. Co., Ltd. (hereinafter referred to as “Regis Success”) is a CRO company focusing on the whole lifecycle service of medical devices. The business scope includes medical device regulatory services, clinical evaluation services, quality management system services and post-market compliance consultation services, providing high-quality and efficient market access services for medical device enterprises.

  The core team members come from listed CROs, TOP20 medical enterprises and clinical research institutions, have been working in the medical device industry for more than 10 years, providing customers with efficient and professional regulatory services, controlling the progress of the project, ensuring the quality of the project, reducing the risk of registration, and assisting in the rapid marketing of the device.


  Professional · Focused · Innovative

  We have been consistent for 18 years

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Service Scope

Our services include Medical Device Registration and File, Clinical Evaluation, Clinical Study, Legal Agent, Quality Management System Supporting, Regulatory Consulting, Innovation Application, Overseas Registration, and Cosmetics Registration.

Medical devices one-stop service, effective communication & feedback, and customer-centered are RS's core values. In addition, we continue to summarize useful information and original articles to keep you up-to-date on NMPA regulation.
Regis-Success Original

Regis-Success Original not only includes Regis’s understanding, analysis, and interpretation of regulatory documents, but also contains the collection and collation of commonly used information in the work. It can help sponsors to better understand the relevant needs of medical device registration and can also be discussed with experts to promote the medical device industry to be more mature and standardized.

Regis-Success Original

We are not only a service provider, but also your friend to advise you on medical device regulations.

Medical device regulations are rigorous and cold, but Regis team hopes to present rigorous and cold regulations to enterprises in a more down-to-earth way through its own work, so as to assist enterprises to understand and meet regulatory requirements and promote the medical device industry to be more mature and standardized.

At the same time, we will collect and collate the commonly used information in the work, hoping to provide an important tool for enterprises to understand the relevant contents of medical device regulations, so that enterprises can be familiar with regulatory requirements rapidly and efficiently and apply it in daily work.

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