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.
Trials before product commercialization, safety, effectiveness, risk analysis, usability.
Generation, design, coordination, and execution of clinical trials for ophthalmic products.
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.
