High-quality starting materials are the foundation of any successful GMP manufacturing campaign. At Symeres, we ensure that every project begins with reliable, well-characterized, and regulatory-compliant starting points.
Our dedicated non-GMP scale-up laboratory specializes in the synthesis of regulatory starting materials, combining decades of synthetic chemistry expertise with state-of-the-art equipment. This allows us to deliver materials that meet the rigorous standards required for GMP manufacturing, while maintaining flexibility and efficiency in early development.
In our facilities, we can run reactions at scales up to 50 liters, supported by four 50 L reactors (QVF and ChemGlass) and multiple 20 L reactors. For purification, we perform large-scale column chromatography on up to 20 kg of silica, ensuring that starting materials are obtained in the purity and quantities required to keep projects on track.
By controlling both the quality and delivery timelines of starting materials, we minimize risk, accelerate project progress, and provide our clients with a seamless transition from research to GMP manufacturing.
Discover Exemplify
We deliver a number of services in partnership with Exemplify BioPharma, a global Partnership Research Organization (PRO) offering end-to-end CMC solutions under one roof.
Exemplify offers:
- Integrated project management across Process Chemistry, Analytical Chemistry, and Formulation Development
- Expert oversight on CRO/CMO selection, contracting, and management
- Comprehensive support with CMC regulatory submissions (IND, IMPD, NDA, MAA)
- Full Quality Assurance and compliance sign-off
- Efficient timeline and budget management
Their newly expanded Formulation Suite also opens the door to enhanced formulation capabilities, strengthening support from early development through to commercialization.
