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I will connect you with reliable biopharma cro cdmo services in china
Chine
Je parle Chinois, Anglais, Japonais
I am a master's degree graduate from Dalian University of Technology. With 8 years of experience in biopharmaceutical analysis, including work experience at a listed company, I currently serve as a Re...
À propos de ce service
Are you a biotech company struggling to find reliable CRO/CDMO partners in China?
You need GMP-compliant suppliers with real expertisebut vetting from afar takes weeks.
Hi, Im Henry. Based in Suzhou, I have 8 years of experience in the biopharmaceutical industry, currently working for a publicly listed CDMO. I help overseas clients connect with pre-vetted, high-quality CRO/CDMOs in China.
What You Get
- Shortlist: 3-5 suppliers matched to your project (ADC, CAR-T, mRNA, AAV, etc.)
- Capability Summary: GMP status, key platforms, regulatory experience
- Direct Contacts: Key account manager details
- Pricing Support: RFQ and quotation consolidation (Standard/Premium)
My Service Areas
Chemical R&D · Biologics · Cell & Gene Therapy · Preclinical & Clinical Support · Sequencing & Plasmid Construction
My Process
- Order & project briefing
- Supplier screening from my network
- Delivery of comparison report (3-5 days)
- Optional: RFQ, negotiation, meeting coordination
Ready to accelerate your project with trusted Chinese partners? Contact me with your requirements.
Domaine:
Business
Industrie:
Biotechnologies
•
Médical et pharmaceutique
Langue:
Chinois (simplifié)
•
Anglais
•
Japonais
FAQ
What types of biopharmaceutical services can you help with?
I cover a broad range, including small molecule R&D and manufacturing, biologics development, cell and gene therapy (ADC, CAR-T, mRNA, AAV), preclinical and clinical support, as well as basic R&D services like sequencing and plasmid construction.
Do you only work with large CDMOs?
No. I work with both mid-sized specialized CROs and larger integrated CDMOs. I match suppliers to your project stage—whether you need early-stage R&D support or GMP manufacturing for clinical trials.
How do you verify the quality and compliance of these suppliers?
I leverage my industry knowledge and network. I only recommend suppliers with relevant experience, proper GMP certifications, and a track record of working with international clients. For Premium packages, I can provide deeper verification.
What information do you need from me to start?
I will send you a brief questionnaire after you place an order. Typically, I need: therapeutic area, desired service type (e.g., process development, manufacturing), stage of development, and any specific compliance requirements (e.g., FDA, EMA, NMPA).
Can you help with negotiation and contracting?
Yes, for Standard and Premium packages I assist with collecting formal quotations and support initial price discussions. For complex contract negotiations, I can help facilitate communication.
What is the typical timeline?
Basic package: 3–5 days. Standard and Premium: 5–7 days, depending on the complexity of your requirements and responsiveness of suppliers.
