Good hospital practice

2.1 Planning the treatment programme

• 2.1.01 Range of services and presentation
• 2.1.02 List of services
• 2.1.03 Development planning
• 2.1.04 Origin analysis

2.2 Planning for the individual patient

• 2.2.01 Admission of a patient
• 2.2.02 Findings on admission
• 2.2.03 Dealing with previous findings
• 2.2.04 Treatment plan and review

2.3 Configuration of the treatment

• 2.3.01 Core process and its support
• 2.3.02 Process management
• 2.3.03 Create treatment pattern
• 2.3.04 Managing and updating configuration documents

2.4 Guidance of the treatment

• 2.4.01 Responsibility for treatment
• 2.4.02 Visit
• 2.4.03 Consultation: Involvement of other doctors
• 2.4.04 Pain therapy

2.5 Aftercare

• 2.5.01 Planning care after discharge
• 2.5.02 Discharge from hospital treatment
• 2.5.03 Withdrawal from hospital treatment against medical advice
• 2.5.04 Medical instructions on discharge

3.1 Responsibility of the management

• 3.1.01 Organisational statutes
• 3.1.02 Organisational structure (organisation chart)
• 3.1.03 Commissions for the professional support of hospital management
• 3.1.04 Authorised representative system

3.2 Occupational safety, health and radiation protection

• 3.2.01 Occupational health and safety
• 3.2.02 Safety instruction, implementation and documentation
• 3.2.03 Behaviour in the event of accidents at work
• 3.2.04 Correcting safety deficiencies

3.3 Hygiene

• 3.3.01 Central hygiene regulations
• 3.3.02 Control tasks in hygiene
• 3.3.03 Hygiene folder
• 3.3.04 Biological hazardous substances

3.4 Resources

• 3.4.01 Grounds and buildings
• 3.4.02 Fire protection
• 3.4.03 Wayfinding system
• 3.4.04 Floor plans

3.5 Procurement

• 3.5.01 General Terms and Conditions of Purchase
• 3.5.02 Supply of medicinal products and medical devices
• 3.5.03 Provision of remedies and aids
• 3.5.04 Selection and procurement of medical equipment

3.6 Services

• Medical services
• Patient-centred services
• Technical-logistical services
• Administrative services

4.1 Documentation

• 4.1.01 Steering Records
• 4.1.02 Signature list hand signal
• 4.1.03 Data protection
• 4.1.04 EDP

4.2 Communication and marketing

• 4.2.01 Meetings: Inviting, organising, reporting
• 4.2.02 Technical means of communication: utilisation
• 4.2.03 Central contact point, information, gateway
• 4.2.04 "Customers" and partner surveys

4.3 Knowledge management

• 4.3.01 Library
• 4.3.02 Literature research
• 4.3.03 Search for guidelines and HTA reports
• 4.3.04 Individual case reports: Composing and searching

5.1 Testing and measurement

• 5.1.01 Audits in QM
• 5.1.02 Validation, verification, calibration of test equipment
• 5.1.03 Test equipment monitoring
• 5.1.14 Inspection of the ward by the pharmacist

5.2 Analysis and validation

• Clinical Trial Manual
• 5.2.01 Evaluation programme
• 5.2.02 Design planning (development inputs)
• 5.2.03 Verification from the literature

5.3 Dealing with risks and opportunities

• 5.3.01 Report on Adverse Events
• 5.3.02 Special incident
• 5.3.03 Incidents involving medical devices
• 5.3.04 Adverse drug reactions

5.4 Improvement measures

• 5.4.01 Improving the acceptability of hospital services
• 5.4.02 Hazard analysis (risk system audit)
• 5.4.03 Corrective and preventive measures
• 5.4.04 Individual case analysis of a UE

6.01 General rules

6.02 Basic skills

• Medical history
• Investigation

6.03 Diagnostic pathways

• Leading symptoms A - C
• Leading symptoms D - G
• Leading symptoms H - L
• Leading symptoms M - P

6.04 Emergency medicine

• 6.4 What is part of emergency medicine?

6.05 Anaesthesia

• 6.05 Anaesthesia and analgesia in obstetrics

6.06 Intensive care medicine

• Historical collection

7.1 Job and duty rosters

• 7.1.14 Gynaecology

7.2 Medical staff

• Coding clinics and institutes

7.3 Nursing staff

• Ward care
• Operating theatre staff
• Intensive care unit
• Functional areas

7.4 Technical personnel

7.5 Personnel administration

7.6 Scientific staff

8.1 Floor plans, room requirements

8.2 Device books

8.3 Diagrams, forms

8.4 Training modules

• Educational films

8.5 Materials

8.6 Tools

A International institutions

• IAF International Accreditation Forum
• ICH International Conference on Harmonisation
• ILO International Labour Organization
• IMDRF International Medical Device Regulators Forum

B National publisher USA

• AHRQ

C Specialist organisations USA

D Various publishers

• Consort

E National publishers Non-EC, non-USA

• Australia

F Specialist organisations Not Eu Not Usa

• Australia
• Canada
• New Zealand