Medical Writing
OWL Oncology provides expert medical writing services that ensure clarity, accuracy, and regulatory alignment across clinical trial documents. From protocols and investigator brochures to clinical study reports and regulatory submissions, our writers translate complex science into precise, compelling content that supports successful trials and timely approvals.
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Why Choose an FSP For Medical Writing
FSPs like OWL offer sponsors expert medical writers without long-term staffing burdens. Sponsors gain flexible, scalable support from professionals who are well-versed in complex therapeutic indications and regulatory requirements. It’s a fast, efficient way to ensure documents are accurate and compliant, without committing to long-term expansion of internal departments.
Submission-Ready Content
From INDs to CSRs, OWL delivers regulatory-grade documents that meet FDA, EMA, and ICH guidelines. Our writers stay current on evolving requirements and industry expectations, helping sponsors avoid delays, reduce revisions, and move confidently through agency interactions with clean, consistent, and audit-ready documentation.
Our Medical Writers Integrate Seamlessly With Your Team
OWL integrates medical writing support directly into your workflow, whether you need help drafting from scratch or polishing team-developed content. Our writers collaborate effectively with clinical, regulatory, and biostats teams to ensure accuracy, consistency, and scientific integrity across all deliverables, without communication bottlenecks.