We help your products enter overseas market quickly
In order to sell medical device overseas, you need to apply for registration. It is not an easy job to deal with all kind of connection, such as different company person, and the health authorities.  

License Biomedical CO.,LTD provides you a total solutions services for license registration. All you need to do is to prepare one set of documentation  
Markets you may be interested in:
Taiwan, USA, EU, China, Southeast Asia, Canada, Japan

˙Documentation Writing and Preparation
To claim the efficacy and safety all medical device manufacturers are responsible for providing technical documentation of their products that conform with the latest regulations. Technical documentation contains product design, verification and validation, risk management, pre-clinical testing, quality control, clinical evaluation, and post-market surveillance programs.
 
However, it can be a challenge for many small and medium-sized manufacturers creating fully compliant technical documentation. License Biomedical CO.,LTD. can help you go through the whole process. Start from clinical or non-clinical trials designing, and create technical documentation for registration and review.

˙Stay up-to-date with the latest international regulatory developments
In most cases, the product registration is sufficient unless the product undergoes significant change. However, products that are already legally available needs to subject to new regulatory requirements. It is important to follow the latest regulatory.
Trust our team, License Biomedical CO., LTD. is expertise and experienced. We can help you navigate the complex registrations, so that you can focus on technology development and marketing.