Generic Drug Development Services
Source: BASi (Bioanalytical Systems Inc)
We know that generic drug development requires a strong CRO lab partner. Developing a bioequivalent demands efficient, high quality, and regulatory compliant analyses at every step.
Click Here To Download:
Brochure: Drug Development Contract Services
Brochure: Drug Development Contract Services
Brochure: Drug Development Contract Services
We know that generic drug development requires a strong CRO lab partner. Developing a bioequivalent demands efficient, high quality, and regulatory compliant analyses at every step. BASi delivers efficient bioanalytical method development and sample analysis as well comprehensive pharmaceutical analysis including stability program support, method validation, and final product release testing. Our scientists will be there supporting you from early phase R&D work to ANDA submission and post-market with sample analysis and stability testing.
Services
Early Phase R&D
- Clinical trial bioequivalence method development
- Clinical trial study sample bioanalytical analysis
- In Vitro bioequivalence comparisons
- More than 1000 proven bioanalytical methods
Pharmaceutical Analysis Services
- Broad array of services from ANDA stability program support to post-commercialization product testing
- Method development and validation
- Stability study program support
- Product release testing
- Comprehensive formulations supported
- Stability storage on site
Benefits
- Quality and cost effective results
- Fast turnaround of data
- Efficient and nimble processes to meet your timelines
- Scientist-to-scientist timely communication
- Strong client partnerships
- Exemplary regulatory record
- Efficient GMP/GLP Services
- Expert technical staff
- Multiple sites in US and Europe
Brochure: Drug Development Contract Services
This website uses cookies to ensure you get the best experience on our website. Learn more