TriLexica Editorial provides consulting in Medical and Technical Writing and Editing with a focus on the Health, Life Sciences, Biotechnology, and Clinical Research industries. Our consultants are available to work remotely as a virtual department on an "as needed" basis, or can be available on-site to supplement your company's existing team. Our Medical Writing and Editing consulting includes expertise with writing and QC per ICH, GCP, and FDA guidelines as well as templates for the clinical and regulatory documentation required for IND, NDA, and BLA submissions. Deliverables include: -Informed Consent Forms -Patient Safety Narratives -Clinical Study Reports (with appendices) -Presentation Slide Sets -Investigator Brochures -Standard Operating Procedures -Templates and training for all of the above Our Technical Writing and Editing experience includes expertise with current trends in IT documentation practices. Deliverables include: -Software Documentation -User Guides -Training Manuals -Policies, Procedures, Work Instructions -EDMS via SharePoint, Livelink, etc NEED WRITING OR EDITING SERVICES NOW? For more information on our Writing and Editing Consulting services contact us via email: admin@trilexica.com