Clinical Trials

Ocupharm Diagnostics S.L it offers through its technical and regulatory department advice, design, coordination, execution, and interpretation of customized clinical trials tailored to the legislation and requirements of each client.

These trials include both pre-commercialization needs and post-commercialization requirements necessary to comply with the new MDR.

Preclinical Trials

Trials before product commercialization, safety, effectiveness, risk analysis, usability.

Clinical Trials (Phases I – IV)

Generation, design, coordination, and execution of clinical trials for ophthalmic products.

Post-Marketing Clinical Follow-Up (PMCF) Trials

Design, depending on the situation, and execution of post-marketing studies based on the collection of clinical data from the use of medical devices in humans.