5.2 Analysis and validation Estimated reading: 1 minute 31 views Authors The hospital's services, in particular the medical and nursing (medical) core services, should comply with the professional rules (of doctors, nurses and other professional groups) and take into account the current state of scientific knowledge. For the individual services, it should be proven that they are suitable to fulfill the expectations placed in them (validation of the services with regard to the essential quality characteristics) and that the services are reliably provided by the hospital in the planned manner (verification). Combinations of therapeutic procedures must be examined separately. The evaluation must be carried out using scientific and technical rules and test theory. It must always be demonstrated whether and to what extent the specified and assumed quality requirements are met. The evaluation should describe the degree of fulfillment and the reliability of the statements with statistical data. Own studies, expert opinions, literature documentation or guidelines from authorized institutions (standards) can serve as evidence for the statements on performance. Several professional groups will always be involved in the evaluation process. The tools of process planning and review should be used. It should be stipulated that research and development activities for new treatment procedures are assigned to qualified personnel who are equipped with appropriate resources. Procedural instructionClinical Trial Manual 1 SCO Scope Purpose and mission 2 MAN Management 3 SUB Subjects Study participants 4 QUS Quality System Quality management system 5 PRS Personal Staff 6 EQU Equipment devices 7 PUR Purchase Procurement 8 CSP Provided products 9 Pro Protocol test planning 10 PRC Process Control Process Control Monitoring 11 Con Conditions Test conditions 12 Data Data 13 Statistics 14 Reporting Reporting 15 Arc archiving 16 SOP Standard Operating Procedures Work instructions 17 EVA Evaluation Validation 18 COM Communication Communication 19 TES Testing Exam 20 CQI Continuous Improvement Improvement 5.2.01 Evaluation program 5.2.02 Design planning (development inputs) 5.2.03 Verification from the literature 5.2.04 Clinical-experimental research program 5.2.05 Ethics Committee 5.2.06 Planning and conducting clinical trials (Clinical Trial Manual) 5.2.07 Risk assessment 5.2.08 Creation of a risk matrix for treatment patterns 5.2.09 Assessment of economic efficiency 5.2.10 Evaluation from guidelines or standards 5.2.11 Examination of the process capability 5.2.12 The design document 5.2.13 Innovation initiative 5.2.14 Design review and release 5.2.15 Introduction of new or modified products 5.2.16 Control of design changes 5.2.17 Verification of laboratory methods 5.2.18 Evaluation of diagnostic tests 5.2.19 Software validation 5.2.20 Statistical methods 5.2.21 Doctoral regulations and doctoral supervision 5.2.22 Habilitation regulations 5.2.23 Health Technology Assessment 5.2.24 Clinical evaluation of medical devices 5 Examination - Previous 5.1 Testing and measurement Next - 5 Examination 5.3 Dealing with risks and opportunities