Objectives: To gain insight into the current implementation of national guidelines on training, examination and registration of proficiencies for the safe use of medical devices and to explore the barriers and facilitators faced during the implementation of these national guidelines. Methods: A questionnaire was sent to all Dutch hospitals and interviews were held with staff at six hospitals. Results: There are differences between hospitals in the implementation stage, but also within hospitals. The questionnaire showed differences between training and examination for devices used by nurses and those used by medical specialists. The interviews showed that most barriers and facilitators for implementation of the national guidelines can be fo...
Background: To improve perioperative patient safety, guidelines for the preoperative, peroperative, ...
The EU medical device (MD) regulatory structure has changed from Directives to Regulations to ascer...
Background: Hospital boards have the responsibility to ensure compliance of hospital staff with guid...
Objectives: To gain insight into the current implementation of national guidelines on training, exam...
Objectives: The aim of this study was to explore the risk assessment tools and criteria used to asse...
OBJECTIVES: The aim of this study was to explore the risk assessment tools and criteria used to asse...
Objectives: The aim of this study was to explore the risk assessment tools and criteria used to asse...
Rationale, aims and objectivesThis study provides insight into how Dutch hospitals ensure that guide...
Rationale, aims and objectives This study provides insight into how Dutch hospitals ensure that guid...
Background: The study was carried out as part of the European Network for Patient Safety (EUNetPas)...
To optimize appropriate antimicrobial use in a university hospital and identify barriers hampering i...
Background: To improve perioperative patient safety, guidelines for the preoperative, peroperative, ...
The EU medical device (MD) regulatory structure has changed from Directives to Regulations to ascer...
Background: Hospital boards have the responsibility to ensure compliance of hospital staff with guid...
Objectives: To gain insight into the current implementation of national guidelines on training, exam...
Objectives: The aim of this study was to explore the risk assessment tools and criteria used to asse...
OBJECTIVES: The aim of this study was to explore the risk assessment tools and criteria used to asse...
Objectives: The aim of this study was to explore the risk assessment tools and criteria used to asse...
Rationale, aims and objectivesThis study provides insight into how Dutch hospitals ensure that guide...
Rationale, aims and objectives This study provides insight into how Dutch hospitals ensure that guid...
Background: The study was carried out as part of the European Network for Patient Safety (EUNetPas)...
To optimize appropriate antimicrobial use in a university hospital and identify barriers hampering i...
Background: To improve perioperative patient safety, guidelines for the preoperative, peroperative, ...
The EU medical device (MD) regulatory structure has changed from Directives to Regulations to ascer...
Background: Hospital boards have the responsibility to ensure compliance of hospital staff with guid...