DiTEBA is a global leader in complex analytical and bioanalytical testing, providing solutions and services to the pharmaceutical, biopharmaceutical and nutraceutical industries.
We support both large and small molecule testing for various dosage forms including solids, semi-solids, liquids, aerosols and other special dosage forms.
Our work is focused in several core areas including: In Vitro Release Testing (IVRT); stability storage and testing; method development and validation; and QC testing at our fully accredited facility.
To be the contract partner of choice for analytical and bioanalytical services.
Our commitment to our customers
DiTEBA will deliver great science and quality excellence, on time, every time.
Our scientific team has extensive knowledge, experience and expertise in analytical and bioanalytical analysis specializing in the ability to resolve the most challenging method development difficulties facing our customers for both large and small molecules.
DiTEBA’s testing services comply with both GLP and GMP and are performed in accordance with the requirements of the U.S. Food and Drug Administration (FDA), Health Canada and the International Conference on Harmonization (ICH).
DiTEBA is licenced by Health Canada as a GMP drug establishment and registered as a drug establishment with the U.S. FDA. DiTEBA is also licensed by Health Canada to handle controlled drugs and substances.