Mincoo is reshaping the skincare industry, the medical aesthetics and pharmaceutical industry, as well as the future of people's lives worldwide. Backed by numerous patents and unparalleled market insights, Mincoo has received multiple certificates and qualifications worldwide.
Mincoo's workshop is designed and constructed in accordance with the requirements of ICH Q7 and the 2010 GMP. The manufacturing process is fully enclosed to minimize contamination. The final filtration using a 0.22 µm filter prevents foreign matter from entering the final purification process. Drying and packaging are conducted in a classified C+A grade clean area, effectively preventing microbial contamination.
Using enzymatic hydrolysis technology to manufacture PDRN products with molecular weights ranging from 100kDa to 3500kDa enables effective and precise control over the product's molecular weight, while the enzymatic process maximizes the product's activity.
We have established a quality management system in accordance with ICH Q7 and the 2010 version of GMP to control raw material collection, transportation, production and packaging, testing, and product delivery.
The manufacturing process has been validated, and throughout the entire production process, from raw material entry to product transportation to the client, pollution, cross-contamination, confusion, and errors are controlled to sustainably and stably produce products that meet predetermined quality standards.
Technical Cooperation and Support
Custom technical support, joint laboratory construction, professional technical consultation & innovative co-creation system
Custom Technical Support
- Adjust concentration, specifications, and dosage forms as required.
- Formula guidance and usage plan suggestions.
- Shorten the R&D and launch cycle of products.
Joint R&D & Laboratory Co-construction
- Support feasibility study at lab and pilot scale.
- Jointly design experimental schemes & research ideas.
- Create differentiated product solutions together.
Technical Advisory Service
- Regular technical Q&A and consultation docking.
- Guidance on the efficacy verification scheme path.
- Assist with filing the application and compliance implementation.
Innovative Co-Creation
- Explore personalized application scenarios jointly.
- Develop compound raw materials & new formulation directions.
- Build complete value loops and expand business models.
| No. | Raw Material Submission Code | Raw Material Trade Name | Remarks |
|---|---|---|---|
|
1 |
000383-13622-1250 |
Sodium DNA |
Molecular weight: 100,000–500,000 Da |
|
2 |
000383-13622-6876 |
Sodium DNA |
Molecular weight: 500,000–1,000,000 Da |
|
3 |
000383-13622-1762 |
Sodium DNA |
Molecular weight: 1,000,000–1,500,000 Da |
|
4 |
000383-13622-7553 |
Sodium DNA |
Molecular weight: >1,500,000 Da |
| No. | Master File Owner | Master File Registration Item Name | Master File Registration Number | Registration/Update Date |
|---|---|---|---|---|
|
1374 |
Shandong Mincoo Biotech Co., Ltd. |
Polydeoxyribonucleotide Raw Material Master File |
M2026155-000 |
2026/04/24 |
Mincoo brings together senior technical experts. With decades of industry experience, we refine raw materials into exceptional ingredients.
