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• Clinical trials in Central and Eastern Europe
• Services
• Phase I. / Bioequivalence
• Phase II.-IV Clinical Trials
• Regulatory Affairs
• Pharmacovigilance
• QA Site Audit Preparation
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Regulatory Affairs

Part of SmartMedico’s expertise is collation, review and development of clinical trial regulatory documents, translation to local languages, submission to relevant Ethics Committees, regulatory application preparation and continuous legislation review/ update.