Our Services

At Rockwood Medical Writing Agency, we deliver precise, compelling, and compliant medical writing solutions across a range of formats and therapeutic areas. Whether you are advancing a product through clinical development, communicating scientific data to stakeholders, or engaging patients and healthcare professionals, our writing is grounded in scientific rigour and tailored to your audience.

Scientific Writing

Our scientific writing services support informed decision-making, stakeholder engagement, and thought leadership. We craft accurate and authoritative documents such as white papers or literature reviews that convey depth of insight while remaining accessible to target audiences.

Publication Support

We provide comprehensive support for the development of high-quality, publication-ready materials that adhere to target journal and congress requirements.

Advisory Board Preparation

We provide expert support in the preparation of high-quality materials for Advisory Boards, ensuring content is clear, data-driven, and aligned with strategic objectives. From briefing documents and pre-read slide decks to meeting agendas and discussion guides, our materials equip advisors with the context they need to offer meaningful scientific and clinical insights.

Marketing & Patient Education Content

We create health-literate, engaging content that empowers patients, caregivers, and the public to better understand their conditions and treatments. All content is crafted to align with regulatory and ethical standards while maintaining clarity and empathy.

Continuing Medical Education (CME) Content

We support the development of unbiased, evidence-based CME content tailored to the needs of healthcare professionals. Our writing ensures scientific accuracy, educational value, and compliance with accreditation standards.

Regulatory Submissions

We provide expert medical writing support for regulatory submissions across all stages of drug and device development. Our services are designed to ensure clarity, scientific accuracy, and full compliance with regional and international regulatory standards, including EMA, MHRA, FDA, and ICH guidelines.

Get a Quote

To request a quote, please get in touch with a brief outline of your project, including the type of deliverable, therapeutic area, and timeline. Costs are based on an hourly rate and will vary depending on the scope and complexity of the work. Once we understand your requirements, we will provide a transparent estimate with no obligation. Whether you need support for a single manuscript or a series of deliverables, we are happy to tailor our services to suit your needs and budget.