STEP 1
STEP 2
STEP 3
STEP 4
STEP 8
STEP 7
STEP 6
STEP 5
STEP 1
STEP 2
STEP 3
STEP 4
STEP 5
STEP 6
STEP 7
1. Consulting details MOQ Raw and subsidiary materials
specification
2. Scheduling
1. Prescription suitability
test & confirmation
1. Commercial contract
2. Quality consignment management contract
3. Confidentiality agreement
1. Stability analysis Harsh environment
testing Preservation testing
2. Toxic substances analysis
3. Subsidiary materials
standard sample confirmation
1. Purchase order receipt
2. Suitability test for manufacturing
facilities and subsidiary materials
3. Product standard preparation
1. Raw and subsidiary
materials purchase
2. Pilot test
3. Manufacturing
4. Filling & packing
1. Quality inspection Semi-complete and complete
products inspection Microorganism inspection COA issue Dispatching sample product for management
1. Development direction consulting Formula, ingredients, etc.
2. Consulting details Price range Distribution network MOQ Raw and subsidiary materials specifications
3. Scheduling
1. Prescription & evaluation 1st development : 2-3 weeks Improvement : 1-2 weeks Prescription confirmation and quoting
2. Licensing Clinical testing request for functionality Quasi drugs licensing Functionality report Safety self-inspection
(household items-limited only in korea)
1. Commercial contract
2. Quality consignment management contract
3. Confidentiality agreement
1. Stability analysis Harsh environment testing Preservation testing
2. Toxic substances analysis
3. Subsidiary materials standard
sample confirmation
1. Purchase order receipt
2. Suitability test for manufacturing facilities
and subsidiary materials
3. Product standard preparation
1. Raw and subsidiary materials purchase
2. Pilot test
3. Manufacturing
4. Filling & packing
1. Quality inspection Semi-complete and complete
products inspection Microorganism inspection COA issue Dispatching sample product for management