Our medical writers focus on their primary goal of providing each study or submission with concise, comprehensible, and well-structured documents. Adhering to the most up to date guidelines and international standards, they create or edit any clinical study document according to your needs and specific requirements.
Whether you need an informed consent form or a full study report, all documents are proofread to ensure the highest quality. In addition, our writers have extensive expertise in preparing posters and other presentations to promote the results of your study for both the public and experts in the field.
We write the entire spectrum of regulatory documents including but not limited to: study protocols and study reports, investigator’s brochures, subject information and consent forms, Investigational Medicinal Product Dossiers, summaries for submission dossiers and briefing booklets, as well as publication manuscripts, conference posters, and presentations.