Medical Substance & Pharmaceutical Manufacturing
Last updated: 2026.04.06
If you have no manufacturing facility of your own, an OEM (contract manufacturing) agreement with a GMP-certified company is required. For smooth registration, we recommend also adding the 'Wholesale/Retail & E-commerce' category.
Key Points
- Medical Substance & Pharmaceutical Manufacturing can be registered with additional documents such as an OEM agreement.
- Sub-type breakdown — Check needed: 2 | Not eligible: 5
- ☑️ Prescription drugs involve strict GMP facility inspections, so non-resident r…
Which sub-types of Medical Substance & Pharmaceutical Manufacturing can be registered?
Check Needed 2
- In vitro diagnostic reagent manufacturing
- Other medical supplies & pharmaceutical-related product manufacturing
Not Eligible 5
- Basic pharmaceutical substance manufacturing
- Biologic drug manufacturing
- Herbal medicine manufacturing
- Synthetic & other finished drug manufacturing
- Veterinary drug manufacturing
Notes
☑️ Prescription drugs involve strict GMP facility inspections, so non-resident registration is effectively impossible. However, OEM of quasi-drugs (masks, hand sanitizers, etc.) or Class-1 medical-device consumables has successful cases of non-resident registration. ☑️ Depending on the item, a 'medical device sales filing' from the competent public health center or a 'medical device import/manufacturing' filing certificate from the Ministry of Food and Drug Safety may be required before business registration.
Have more questions about registering Medical Substance & Pharmaceutical Manufacturing?
About the author
COWORKCITY CX Team
Customer Experience Team
Experience
- 30,000+ business registration consultations handled across business types
- Business-type suitability verified and managed across 180+ branches nationwide
- Specialized guidance for licensed and OEM business registrations
- Analysis of rejected registrations by business type and FAQ management