Lexitas provides the full range of clinical operations services including study management, site selection, site qualification, regulatory document collection, site management, recruitment strategy development, investigator training and other key clinical operations tasks. Read More
The Lexitas team provides all aspects of clinical monitoring from pre-study to closeout. We are adept at monitoring studies using paper CRFs or with eCRFs.
The Lexitas team has decades of experience with clinical study design and with the development of clinical protocols in the ophthalmology therapeutic area. Lexitas also provides Clinical Study Report writing services and has partnerships with medical writers for more involved regulatory/medical writing projects.
Lexitas has extensive experience in ophthalmic medical affairs. We provide manuscript preparation, generation of scientific messaging and slide decks, abstract and poster production, medical information letter creation and trade journal placement.
Lexitas will provide medical monitoring services when your team requires the input of an ophthalmic medical expert experienced in clinical trials.
Through partnerships with service providers focused on data management and biostatistics, Lexitas provides a full service solution.
Lexitas also has relationships with complementary providers in the areas of EDC, IVR, and other clinical trial technologies. We are able to help you with evaluation, selection and management of clinical trial technology vendors.