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Unrivalled expertise in small molecule analysis, development, and manufacturing
Solvias can help you navigate the complex small molecule development journey. Our ability to flag potential issues early helps minimize surprises during clinical trials, avoiding costly delays.
Broad capabilities
We stand by you throughout the product life cycle. Our analytical solutions are tailored to ensure the supply, purity, potency, consistency, and safety of your small molecules, reducing risk at every step through comprehensive small molecule analysis
Drug substance development & manufacturing capabilities
Integrated chemical and analytical development for early phase drug substance development, manufacturing and analytical CMC services across the full life cycle.
Drug substance & drug product analytical CMC capabilities
Comprehensive characterization and release services covering all major dosage forms and complex delivery systems, including OINDP.
Impurity and contamination control
Expert services, from initial profiling and risk assessment to commercial control strategy.
Raw materials, excipients, and packaging testing
Comprehensive services offering reliability, flexibility, and quality to support raw material and excipient analysis and E&L testing.
Fully integrated analytical CMC and API development solutions across the product life cycle
We offer integrated Chemistry Manufacturing and Controls (CMC) solutions throughout the entire product life cycle, from early stage to late stage to commercialization. We offer you:
- Seamlessly integrated synthesis, catalysis, and solid state analytical characterization services
- Efficient, timely supply of high-quality, early-phase material and processes
- Technology, dedicated expertise, and track record of success with complex chemistry
- Phase-appropriate strategies help avoid issues later in development, mitigating risk through thorough small molecule analysis
- Comprehensive programs including analytical development, validation, stability and release testing for drug substance and drug product
Access to expertise
With a 25-year legacy, our scientific, regulatory, and project management expertise helps our clients bring safe products to market. Whether it’s a large program with a dedicated project manager or one-time troubleshooting, we provide direct access to our experts—ensuring scientists can interact with scientists.
Commitment to quality
At Solvias, our dedication to excellence is evident in everything we do. From the stringent quality standards we uphold to the state-of-the-art technologies we employ, including cutting-edge small molecule analysis, we strive to deliver the highest level of cGMP-compliant services globally. We’re not just a service provider; we are your partner in reaching your commercialization goals.
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