Ocupharm diagnostics S.L

Company specialized in assistance and help with the research, development and regulation of ophthalmological products.

Clinical Trials

Ocupharm Diagnostics offers, through its technical and regulatory department, advice, design, coordination, execution and interpretation of personalized clinical trials adjusted to the legislation and requirements of each client.

These trials include both pre-marketing and post-marketing needs necessary for compliance with the new MDR.

Preclinical trials

Tests prior to the marketing of the product, safety, effectiveness, risk analysis, usability.

Clinical trials (Phases I – IV)

Generation, design, coordination and execution of clinical trials of ophthalmological products.

PMCF post-marketing trials

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