DiTEBA provides full-service analytical laboratory testing services, offering a comprehensive array of GLP and GMP compliant analytical chemistry services for the analysis of active pharmaceutical ingredients, inactive ingredients, in-process materials and finished goods.
DiTEBA utilizes the brightest academic ideas and scientific solutions to provide more flexible and R&D-intensive solutions for your drug development needs. These are:
“We are very pleased we contracted DiTEBA for a wide range of GMP/GLP analytical work for both biomolecules and small molecules in various dosage forms and drug development stages, including Phase 1 to Phase 3 products. The work included method development, validation, drug product release and stability programs. Their staff was supportive, well-informed and experienced with the most up-to-date scientific methods, quality practices and regulatory requirements.”
- Theresa Horne, MSc. – Director, Analytical Chemistry