Life science industrie

Clinical Operations

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.

Pharmacovigilance

Regulatory Affairs

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.

Technology background, from series best concept of global business

Pharmacovigilance

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.