PartnershipUpdated on 17 February 2026
EU GMP Clinical Manufacturing Partner for Phase I Supply
About
We are seeking an EU-based GMP partner to support clinical manufacturing and supply for Phase I, with a focus on execution quality, speed, and clean tech transfer discipline.
Partnership scope can include:
-
Optimization for clinical manufacturing readiness and scale-appropriate execution
-
GMP batch execution and quality systems alignment
-
QC strategy support (release logic, stability approach, documentation)
-
CMC documentation contributions suitable for clinical entry
We value partners that are transparent, pragmatic, and comfortable operating on milestone-driven plans. Details can be shared under CDA.
Organisation
Similar opportunities
Expertise
CMC Leadership for Biologics: From Concept to Commercial Manufacturing
- Biotech, Pharma and Cosmetics
Ramtin Rahbar
Co-founder and Chief Technical Officer at Ness Therapeutics
Toronto, Canada
Project cooperation
EU work packages to accelerate Phase I readiness
- Execution
- Technical
- Biotech, Pharma and Cosmetics
Ramtin Rahbar
Co-founder and Chief Technical Officer at Ness Therapeutics
Toronto, Canada
Expertise
Clinical Operations and Project Manager/Clinical Trial & Data Manager
- Healthcare
- Biotech, Pharma and Cosmetics
Madhuparna Ganguly
Clinical Operations & Project Manager | MBA candidate at Swiss Tropical and Public Health Institute
Zurich, Switzerland