Teelia CRO supports all steps of clinical trials from the startup to the final study report.
We intervene in Phase I, II, III, IV as well as epidemiological studies.
Teelia support all regulatory affairs activities from initial dossier for marketing authorization request to post-approval activities.
We manage all activities related to a product portfolio or specific geographical zone.
Teelia helps its clients to identify, prevent, assess, mitigate and report potential and effective risks.
Since 2017, our Indian platform delivers a full ICSRs processing service from the intake until the submission.