· Home > R&A Dept > Quasi Drug ① Preparing lab facility and storage ( allowed to use 3rd party's lab facility and    storage partially or fully ) ② Registering import manager ( Copy of pharmacist license, Medical report,    Certificate of employment, Contract of using a testing lab facility & storage) ③ Registering Korera Pharmaceutical Traders Association ④ Install EDI system ⑤ Reviewing ingredients and documents & setting guidelines for permission ⑥ Declaring the item as quasi drug ⑦ Proceeding clinical test & non-clinical test ⑧ Declaring estimated import & obtaining approval ( Submitting Certificate of    manufacturing & Certificate of free sales) ⑨ Testing in accordance with criteria and appropriate test method ⑩ Providing Korean label ⑪ Drawing up import management book