Porton Advanced
End-to-end ATMP CDMO from cell banking to commercial manufacturing
End-to-end ATMP CDMO provider offering cell engineering, lentiviral vectors, mRNA/LNP, plasmid development, and GMP manufacturing from preclinical through commercialization with 24 IND approvals across NMPA, FDA, and MedSafe. Headquartered in Suzhou, China.
Modalities
Development & manufacturing
Structured CDMO capabilities from verified public sources.
Manufacturing (M)
Regulatory clearances
Services
- Cell-Line Development
- Cell Therapy Manufacturing
- Autologous Cell Therapy Manufacturing
- Allogeneic Cell Therapy Manufacturing
- Lentiviral Vector Manufacturing
- AAV Manufacturing
- Viral Vector Manufacturing
- mRNA Manufacturing
- Lipid Nanoparticle (LNP) Formulation
- CMC Analytical Development
- Process Development
- Technology Transfer
- CMC Regulatory Submission Support
- Sterile Fill-Finish & Aseptic Manufacturing
About this organization
Porton Advanced is a specialized CDMO focused on Advanced Therapy Medicinal Products (ATMPs), providing integrated services from early research through commercial manufacturing. Core capabilities include:
Cell Engineering & Gene Therapy:
- CAR-T, TCR-T, and CAR-NK cell therapy manufacturing
- Autologous and allogeneic cell engineering
- iPSC-derived cell therapies
- MSC cell therapy
Viral Vectors & Nucleic Acids:
- Lentiviral vector manufacturing and GMP production
- Adeno-associated viral (AAV) vector development with proprietary AAVantage® capsid library platform
- mRNA and lipid nanoparticle (LNP) formulation and manufacturing
- Plasmid development (supercoiled, linear, LcDNA)
- Vector construction and plasmid preparation services
CMC & Analytical Services:
- Process and analytical method development
- Cell banking and characterization
- GMP manufacturing for drug substance (DS) and drug product (DP)
- Investigator-initiated clinical trial (IIT) support with integrated clinical data collection and analysis
Regulatory Track Record:
- 24 IND approvals across NMPA (17), FDA (6), and MedSafe (1)
- 100% submission success rate
- 400+ GMP batches manufactured
- 30+ IIT projects completed
Global Manufacturing Footprint: Multiple GMP-compliant facilities across China (Suzhou, Chongqing, Shanghai, Jiangxi, Hubei), United States (New Jersey), and Europe (Denmark, Belgium, Slovenia, Switzerland) supporting DS and DP manufacturing.
Locations
Ascendas Park Campus
Suzhou · Jiangsu · China
Sangtiandao Campus
Suzhou · Jiangsu · China
Cranbury Campus
Cranbury · New Jersey · United States
Chongqing Beibei R&D Site
Chongqing · Chongqing · China
Chongqing Changshou Manufacturing Site
Chongqing · Chongqing · China
Chongqing Beibei Manufacturing Site
Chongqing · Chongqing · China
Shanghai Minhang R&D Site
Shanghai · Shanghai · China
Shanghai Fengxian Manufacturing Site
Shanghai · Shanghai · China
Shanghai Pudong R&D and Manufacturing Site
Shanghai · Shanghai · China
Jiangxi Yichun Manufacturing Site
Yichun · Jiangxi · China
Hubei Xiaogan Manufacturing Site
Xiaogan · Hubei · China
J-STAR South Plainfield R&D Site
South Plainfield · New Jersey · United States
J-STAR Cranbury R&D Site
Cranbury · New Jersey · United States
Porton Advanced Shipping/Logistic Center
Cranbury · New Jersey · United States
Copenhagen Office
Copenhagen · Copenhagen · Denmark
Turnhout Office
Turnhout · Turnhout · Belgium
Slovenia R&D and Manufacturing Site
Ljubljana · Ljubljana · Slovenia
Root Office
Root · Root · Switzerland
Recent news about Porton Advanced
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