We can help you with the creation of medical technical, procedural, informational, educational and promotional materials related to clinical research and clinical practice in accordance with the legislative requirements and formalities for clinical trials of drugs, clinical trials of medical devices, clinical studies investigating diagnostic and therapeutic methods, prospective and retrospective data collection, etc. - Comprehensive and partial services:

• Preparation of documents required for the approval, conduct and termination of a clinical trial - e.g. study protocol, patient information and informed consent, Investigator's Brochure, laboratory or pharmacy manuals, patient diaries, clinical trial summary reports, summaries of study results for the general public, etc.
• Assistance in writing various types of scientific publications related to clinical research projects
• Assistance with the development of educational materials for professionals related to specific clinical research projects
• Consultation or review/revision of documents created by you