Speed Laboratory is cGMP, FDA registered and DEA License (schedule I-V). You need accuracy and reliability – our chemists and microbiologists are here to solve your complex pharmaceutical problems.
Speed Laboratory understands that scientifically sound, legally defensible analytical data is one of the most critical elements for the success of an analytical project. To ensure a project’s data quality objectives are met, Speed Laboratory provides a superior standard of service along with our commitment to customer satisfaction.
- API Analysis
- Bioequivalence Analysis
- Cleaning Validation
- Clinical Trial Material Manufacturing
- Contaminant Identification
- Counterfeit Analysis
- Custom Synthesis
- Degradation Analysis
- Disintegration Studies
- Dissolution Studies
- ELISA Assays
- Excipient Base Identification
- Extractables & Leachables
- Formulation Optimization
- ICH Stability & Release Testing
- IND & NDA Submission Support
- Investigative Chemical Analysis
- Litigation Support Services
- Method Development & Validation
- Overcoming Solubility Issues
- Pre-FDA & Post-FDA Audit
- Pre-Formulation & Formulation
- Production Risk Management
- Purity/Impurity Analysis
- Raw Material Qualification
- Solid Stage Characterization
- Syringability, Injectability, & Inhalation Study
- USP Monograph Testing