Scientific & Medical Writing

Clear and competent presentation of the scientific and research statements and conclusions is an essential phase in any clinical trial.
We offer our medical writing expertise and skills of organizing quality documentation flow throughout the study. Our experts can provide all the medical documentation you need: Protocols, including Synopses and Amendments, ICFs, CSRs, Safety documents, SOPs, IBs, Regulatory responses, IM materials, Dossiers, Manuscripts, Abstracts and so on, from the preclinical phase through the clinical development cycle to post-marketing and commercialization writing.

Our Medical Writing team has expertise in a multitude of study designs and therapeutic areas. Our Medical Writing experts work directly with you, supported by our Regulatory and Quality Assurance teams to meet your needs and ensure complete consistency with all regulatory requirements.