Clinical
Studies Support- Full service clinical study assistance
from protocol development through regulatory approval.
Clinical
Data Management- Expertise in using and developing state-of-the-art
commercial and proprietary systems in support of clinical trials, safety
and post-marketing services.
Pharmacovigilance- Safety monitoring and periodic report submission for approved
drugs and treatment under study.
Since 1986, KAI
has provided creative, cost-effective, and practical
support to the pharmaceutical, biologic, and related industries,
as well as the National Institutes of Health (NIH).