Providing support and expertise in area of healthcare product registration and warehouse/storage registration to the company and/or customers.
Ensure compliance with Thai FDA rules and regulations (Drug ACT).
Register, control and renew all required licenses for the company as Importer and distributor.
Inspect and release incoming commercial goods and returned goods before market/resold/destroy as GSDP requirement.
Establish AE report (Adverse Event), coordinate with the product owner, and follow up AE case.
Monitor Clinical Trial activity according to DPI.