Clinear Research combines medicine, science, and technical writing, and collaborates with medical monitors, scientific experts and sponsors to deliver concise documents for all stages of regulatory, project management, and final reports.

Clinear Research  proposes medical writing assignments such as:

• Protocols and Amendments
• Investigator’s Brochures
• Investigational Medicinal Product Dossiers
• Investigational New Drug documents and Applications (NDAs)
• Clinical Study Reports
• Literature research
• Technical document
• Case Narratives
• Abstracts and Manuscripts
• Documentation for Presentations (abstracts, posters, and slide presentations)
• Risk Management Plans 
• Common Technical Document 
• Trial Master File and Investigator Master File.
• Patient Informed Consent Forms (PICFs)
• FDA Briefing Documents
• IND Annual Reports/ DSURs
• Package Inserts
• Patient Narratives
• Executive Summaries for Efficacy or Safety