Our experienced team of Medical Writers come from diverse backgrounds offering a wide range of expertise. All have PhD’s or MBBS and are experienced in preparing manuscripts for scientific, medical, regulatory and lay audiences. Examples of the types of documents we can produce include:

• Clinical trial protocols 
• Investigator Brochures - to ICH standard
• Patient information and consent forms
• Ethics submissions
• Clinical Trial Reports – interim and final – to ICH standards
• Clinical Trial Summaries
• Clinical Trial Manuals
• DSMB Reports
• Adverse Event and Serious Adverse Event Narratives
• Product Information Sheets 
• Manuscripts for peer-reviewed publications
• Newsletters
• Abstracts 
• Posters
• Literature searches and reviews
• Review and summary of scientific articles and manuscripts

Our written work undergoes a multi-step quality control and review process, to ensure a high quality and professional document is delivered in a timely manner.