Quasi-Drugs Manufacturing & Sale

The new regulations (after 25th Dec, 2014) can be summarized as follows.

License for manufacturing or selling quasi-drugs is required
(There’s only one license type for the quasi-drugs, but quality management may differ according to drug type.)
It should be fully acknowledged which product is eligible for quasi-drugs.
The precedents also should be considered. Ingredients, usages, and standards, and test methods should be compared with the existing products so as to determine whether it is initial application and then application document can be reviewed.
We have lots of experiences in quasi-drug accreditation.

Please contact us for the details.

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