Medical writing is an established core function at Clinart. The medical writing team is fully integrated with the medical monitoring, pharmacovigilance, and biostatistics teams. The input of our veteran research clinicians, statisticians, and bench scientists ensures that our client's key messages are medically and scientifically sound and acceptable to the clinician and researcher alike.

The group skillfully handles writing projects related to drugs, biologics, and medical devices.    Our writers have experience with complex medical research topics such as proteomics, epidemiology, and pharmacogenomics. Clinart has established procedures for document management and a broad collective experience in current electronic submission formats and standards. Our documents undergo rigorous quality assurance review before delivery to our clients.

• Clinical Study Reports
• Protocols
• Informed Consent Documents
• Pediatric Assent Forms
• Literature Reviews
• Abstracts/Presentations