Urtech Medical Writing & Consultancy LLC - Medical Writing Services

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arrow Clinical Protocols, Informed Consent Documents, and Amendments
clinical study reports ICH-compliant Clinical Study Reports, Phase I through Phase IV
patient narratives Patient Narratives
project management Project Management
review Reviews
NDA Consultation on New Drug Applications based on the Common
CTD Technical Document format and specifications, including writing of
ICH module the clinical content for Modules 2 and 5.
SOPs Standard Operating Procedures
regulatory Briefing Documents
clinical trial disclosure Clinical Trial Disclosure
abstracts Abstracts and Summaries
manuscripts Journal Manuscripts
posters Posters