Import Registration Service
Our team has more than 20 years of import and export drug registration experience, has successfully registered more than 100 products
Import and export countries or regions: EU, Japan, Korea, Southeast Asia, South America, Middle East and North Africa, etc
Service
1.Project evaluation
2.Registration Consulting Training
3.Translate, write, compile and review the application materials
4.Organize the declaration of expert meeting
5.Register for approval, receive and send official notice
6.Assist in receiving samples and reviewing standards
7.Technical support for on-site verification
Our strengths and advantages
1.Perfect and standard registration declaration management system to ensure the standardization of the registration process;
2.Professional teams translate and compile the application materials, and experts strictly check and verify the materials, so as to be familiar with the evaluation criteria and shorten the application period.
3.In-depth and comprehensive project approval and market research to ensure sufficient basis for project approval;
4.Years of mature experience in communicating with manufacturers, good and close relationship with pharmaceutical administration department.