Cromos Pharma has vast experience in providing a wide range of CRO services to support the development of new treatments and interventions for various eye-related disorders
We have specialized expertise in designing and conducting clinical trials for ophthalmic drugs, medical devices, and surgical procedures. Our experience includes working with a range of ophthalmic conditions, including age-related macular degeneration, diabetic retinopathy, glaucoma, and dry eye syndrome.
We offer our sponsors support in ophthalmologic clinical trial design. Cromos Pharma works closely with its clients to develop clinical trial protocols that are scientifically rigorous and easily meet regulatory requirements. We help our sponsors to identify appropriate endpoints and outcome measures to assess both safety and efficacy of their investigational products. We are experts in creating investigator brochures and other regulatory documents. We can also provide support for publications and presentations that address clinical trial results.
Cromos Pharma has extensive knowledge of international regulatory requirements for ophthalmologic clinical trials and can help its clients navigate the complex regulatory landscape. We provide support for regulatory submissions in EU via CTIS and in the US, including INDs, NDAs, MAAs, and BLAs, and can help our clients prepare for meetings with regulatory agencies.
Cromos Pharma provides a wide range of specialized services to support the development of new treatments and therapies for eye-related disorders. Our expertise in clinical trial design, data management and analysis, regulatory support, medical writing, and quality assurance can help our clients bring new ophthalmic products to market more efficiently and effectively.