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The Clinical and Medical Writing team at Lexitas Pharma Services specializes in the creation and development of high-quality regulatory and scientific documents. They are responsible for drafting protocols, clinical study reports, investigator brochures, and submission-ready documents for INDs and NDAs. Their work ensures clear, precise, and compliant communication of clinical trial data and regulatory information, supporting the seamless progression of innovative ophthalmic therapies from concept to patient care.