Clinical studies are determined by a variety of legal and regulatory requirements. Successful approval of clinical trials is only possible if the clinical studies are planned and carried out in these regulated environments. SCHOLZ Pharma GmbH offers you services in connection with the clinical development of pharmaceuticals in the following scope:
• Contract Research Organization audits
• Audits from testing centers
• Create and maintain the trial master file
• Training for investigators, monitors
• Document Management: Creating & Reviewing Study Documentation, Enrollment Application / EC / CA Approval, Study Design, Study Plan, CRF, Patient Information, Study Reports