Moravek is licensed by the California Department of Public Health, Food and Drug Branch, for the preparation of active pharmaceutical ingredients (API) for research. In addition, Moravek is allowed to handle schedule I-V classified compounds under DEA authority.
Moravek is able to perform custom synthesis, purification, and testing for a wide range of chemical compounds. Our custom synthesis services provide trusted solutions for your research project.
Non-labeled compounds produced or purified under non-GLP conditions are accompanied by HPLC co-elution with reference standards, mass spectrometry, and NMR to ensure that your product is of the highest quality. Our expert chemists provide the custom synthesis services that meet your specifications and all regulatory requirements.
Production of non-GLP materials includes, but is not limited to:
Analysis & Documentation
- Certificate of Analysis certifying non-labeled product meets the agreed upon specifications
- HPLC, MS, and NMR analysis (as appropriate)
- Chemical stability data (optional)
- Utilization of qualified analytical equipment (optional)
Logistics & Customer Service
- Weekly email updates
- Initial (kick-off) teleconference (optional)
- Confirmation of storage/packaging conditions
- Shipping & storage tracking
Shipping & Storage
- Aliquot preparation
- Domestic & International door-to-door shipment
- Secure storage at ambient, +4°C, -20°C, or -80°C
- Temperature logging during shipment (optional)
* Products produced under non-GMP guidelines are not suitable for clinical trials