Serving as our client's extension, we offer clinical pharmacology support in the following areas:
We have extensive experience in Phase 1 studies including single- and multiple- ascending dose studies, bioavailability/bioequivalence (BA/BE), drug-drug interactions and special populations studies.
We use a platform technology of industry-standard, validated softwares that supports 21 CFR part 11 compliance with a full audit trail, version control and electronic signatures.