Strategic support at each step of the process from document structure through targeted messaging. Generate written content from raw data, write cover letters or carefully worded responses to reviewers. Assist with target journal selection. Submit to the journal or conference.

Identify opportunities. Navigate the expansive list of governmental funding agencies and private foundations to provide a descriptive list of appropriate grants and corresponding deadlines. Complete registrations required to meet eligibility requirements. Prepare components of applications, from the abstract and research strategy to the commercialization plan.

Work with cross-functional teams to generate clinical study protocols, FDA response documents, orphan drug or breakthrough designation applications, and preclinical and clinical study reports. Perform systematic literature searches and comprehensive reviews for post-market approval and safety reports.

Create clearly written, professionally polished documents that reflect the voice of your company: content for white papers, application or technical notes, brochures, newsletters, blogs, or other web or print content.

Our writers are experienced research scientists and are available for consultation on a variety of projects ranging from experimental design and surgical training to project management.