Preclinical Drug Development CRO/CDMO Services
One-stop solutions from drug discovery to preclinical development
Professional biomedical R&D service provider, offering small molecule chemistry, nanobody, ADME/DMPK, oncology research and GMP manufacturing services to biotech companies - Faster, Better, More Cost-Effective solutions
Our Services
Professional preclinical R&D services to accelerate your drug development
Small Molecule Chemistry
Custom synthesis from mg to kg scale, 100+ professional chemists, 2-week rapid delivery
- Custom synthesis: mg to kg scale
- Medicinal chemistry optimization
- Process development & scale-up
- Team led by former Merck scientists
Nanobody Development
7-day rapid discovery platform, 160+ validated targets, proprietary llama farm
- 7-day rapid discovery workflow
- 160+ validated target experience
- 12-acre llama farm
- Multiple display platforms (phage/yeast)
ADME/DMPK Services
Comprehensive in vitro and in vivo PK assessment, supporting rapid screening and optimization of drug candidates
- In vitro ADME (solubility, permeability, metabolism)
- In vivo DMPK (PK/PD studies)
- Multiple animal models
- Rapid professional reports
Oncology Research
CDX/PDX/Syngeneic models, professional in vivo efficacy assessment, accelerating anti-tumor drug development
- Multiple mouse models (CDX/PDX/Syngeneic)
- In vivo efficacy assessment
- Biomarker analysis
- Novopath proprietary platform
CDMO/GMP Manufacturing
FDA/EU/China GMP compliant, 50L-10,000L production capacity
- Process development & optimization
- GMP manufacturing (multi-country certified)
- API production
- 50L-10,000L reactors
FDA Consulting Services
Regulatory filing preparation and consulting, 20+ years experience ensuring submission success
- FDA filing preparation
- Regulatory consulting
- Submission strategy planning
- 20+ years regulatory experience
Why Choose Key2Meds
Four core advantages to ensure your project success
Faster
Accelerate project timelines
Rapid milestone delivery
Better
High-quality data support
For funding and regulatory submissions
Cost-Effective
Flexible collaboration models
FTE/FFS on-demand options
Comprehensive
One-stop solutions
From discovery to preclinical
Our Strength
Numbers speak, professionalism trusted
Core Technology Platforms
Unique differentiated technology advantages
PCN Precision Delivery System
- Uncompromised precision, protecting every payload
- Smart pH-responsive release mechanism
- Clinically ready, scalable production
OBOC Peptide Discovery Platform
- Millions of unique peptide compound library
- Diversified screening and intelligent optimization
- Widely applied to targeting ligands and linkers
Nanobody Platform
- 12-acre proprietary llama farm
- Multiple display platforms (phage/yeast/rapid discovery)
- 7-day rapid workflow
Service Process
Five-step process for seamless collaboration
Consultation
Free project assessment
Solution Design
Customized R&D plan
Project Execution
Expert team implementation
Quality Delivery
Data & report delivery
Ongoing Support
Follow-up optimization
Our Certifications
Passed 600+ government and client audits, compliant with global regulatory standards
Client Testimonials
Hear from our partners
"Key2Meds' nanobody platform helped us complete critical target validation in 3 months. The high-quality data supported our successful Series A funding."
"Their chemistry team is highly professional. The scale-up from mg to kg went smoothly with strict quality control and on-time delivery."
"CDMO services are FDA-compliant and helped us pass regulatory review smoothly. The project management team communicates promptly and responds quickly."
Latest News
Stay updated with Key2Meds' latest developments
Key2Meds Completes New Funding Round
The company announced completion of Series B funding, which will be used to expand production capacity and technology platform R&D...
Read More →Nanobody Platform Adds New Validations
Successfully validated 20 new targets, further solidifying our leading position in the nanobody field...
Read More →CDMO Facility Passes FDA Audit
Facility successfully passed FDA on-site audit, quality system highly recognized...
Read More →Ready to Start Your Drug Development Project?
Our expert team is ready to provide customized solutions
Accelerate your drug discovery and development process
Or contact us via:
Email: shawnmu02@yahoo.com
Business Hours: Monday-Friday 9:00-18:00 (Beijing Time)