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Authorised Representative BfArM CE Mark Classification Clinical Studies Code of Conduct Competent Authority Diagnostic DIMDI Ethics Europe Executive Federal Law First Placing G-BA Germany Government Government Affairs InEK In Patient In vitro IQWiG Law Legislative Lobbying Manufacturer Market Medical Apps MPG NUB Out Patient PKV Private Health Insurance Public Affairs Public Relations Register Reimbursement Risk Serious Adverse Events Software The Bundesrat The Bundestag The Federal Institute for Drugs and Medical Devices The Federal Joint Committee The Institute for Quality and Efficiency in Healthcare