Services & Products
De-risk Your Drug Development Projects With Analytical Testing Services Designed by Trusted Experts
Choose from our comprehensive analytical testing packages, custom synthesis and GMP CDMO services.
Conducted entirely in-house, our offerings conform to the latest regulatory guidance with faster turnaround times.
Ligands & Fiber-Optic Products
Secure your drug development process with our advanced monitoring technologies, high-quality process sampling equipment, and extensive ligand and catalyst portfolio.
Quality & Regulatory
Regulatory Strategy Tailored to Your Needs and Built on the Latest Guidance
Solvias holds authorizations to perform pharmaceutical analyses for CMC packages and produce active pharmaceutical ingredients (API) for clinical trials.
We customize and perform analytical tests for each drug substance and product within the standard of Good Manufacturing Practice (GMP). All Solvias facilities are ISO-certified and regularly inspected by licensed authorities, in accordance with the Pharmaceutical Inspection Convention/Cooperation Scheme (PIC/S), the Directives of the European Commission and the Food and Drug Administration (FDA).
Recognizing that a one-size-fits-all approach doesn't meet everyone's needs, Solvias offers each of its partners tailored, cutting-edge solutions.
At Solvias, we combine the attention to detail of a small CRO with state-of-the-art analytical capabilities. This approach has earned us the trust of over 700 customers, including 19 of the top 20 pharmaceutical companies.
5 Sites Across
Europe and the US
of lab capacity
More than 175