Our Services

Drawing on years of experience in designing and conducting clinical trials, Linical helps clients produce a quality protocol that meets study objectives and regulatory requirements.

Linical's Regulatory Affairs team provides global expertise and resources to help with regulatory strategy, meetings, filings.

Quality is the cornerstone of Linical, and our services span SOP’s to QA consulting and audits across the globe.

The Linical medical writing team draws on extensive industry knowledge and therapeutic expertise to effectively meet clients’ product development needs.

Linical is your gateway to experienced clinical trial sites across the globe. Our partnerships with top sites and efficient study start up processes mean your clinical trial will be up and running quickly.

Effective project management is the cornerstone of any trial, and Linical’s experienced project teams work as your partner, helping your trial get completed on time, within budget, and with the quality data you expect.

Linical offers a comprehensive suite of clinical pharmacovigilance and safety monitoring services in a variety of therapeutic areas.

Linical provides global monitoring and site management solutions to our clients via our international team of experienced professionals.

Linical’s biometrics team powers you with the insights you need into every phase of your trial. Our knowledgeable data managers and biostatisticians deliver high-quality solutions tailored to your needs.

Through blending conventional tactics with innovative ideas, Linical provides a comprehensive, global strategy to find the RIGHT patient/subject for your trial.

Linical offers best-in-class training academies for clinical research sites, clinical trial managers, and clinical research associates.