Sail Health has registered in FDA and gotten local and national government support. We own professional team managing the whole registration and approval process efficiently, especially in registration risk prediction and control.
Mission
* Decrease the registration risk.
* Control the registration cost
* shorten the registration period

Health food registration
The definition for health food in China: Special food which is suitable for the given people and can support some function of the wellbeing.
Application procedure
* Select special function for health food
* Test
* Prepare the documents and products for registration
* Fill in application form
* Evaluate and judge by SFDA
* Revise and update the documents
* Reevaluated by SFDA
* Approved by SFDA
* Issue the Certificate of Import Health Food

Cosmetics registration
There are two kinds of cosmetics-general cosmetic products and cosmetic products with functions.
Application procedure
General cosmetic products
* Test
* Prepare the documents and products for registration
* Fill in application form
* Revise and update the documents
* Approved by MOH
* Issue the Certificate of Import General Cosmetics

Cosmetic products with functions.
* Select special function for the product
* Test
* Prepare the documents and products for registration
* Fill in application form
* Evaluate and judge by MOH
* Revise and update the documents
* Approved by MOH
* Issue the Certificate of Import Cosmetic Products with Functions.

Drug registration
* Import drugs should the properties as following:
* Manufacturing process completed outside China
* Drug approved for sale in the country or territory of manufacturing
* Factory which manufacturing the drug(to China) is solely for sale and use
Application procedure
Pre-clinical research
Application submission for approval of clinical research
Evaluation by SFDA
Obtain approval of clinical research
Clinical research
Applying certificate for free sale of the drug
Evaluation by SFDA
Issue the Certificate of Import Drug

Medical device registration
In China, medical device is divided to three classes for administration according to structure feature, use form and use condition.
ClassⅠ-only use on skin surface or used as connector or medical equipment
ClassⅡ-the active equipment applied to the slight lesion indirectly affecting invitro diagnostic reagent
ClassⅢ-the Medical device which direct contact with drug, implanted in human body and used for corporeal circulation(ECC) system
Application procedure
* Standard preparation
* Testing
* Application submission
* Technical review by evaluation center
* Administrative review
* Issue the Certificate of Import Medical Device

Disinfectant registration
Disinfectant is an agent,such as heat, radiation,or chemical,that destroy, neutralize,or inhibits the growth of disease-carrying microorganisms.
Due to Chinese regulation,it is prohibited to produce,import,and sale any disinfectant without approval from Ministry of Health of People's Republic of China
Application procedure
* Sample testing
* Prepare the documents and products for registration
* Fill in application form and submit
* Technical review by evaluation center
* Revise and update the documents
* Approved by MOH
* Issue the Certificate of Disinfectant