Background: Recently, the European Union has introduced the Falsified Medicines Directive (FMD). Additionally, in early 2016, a Delegated Act (DA) related to the FMD was published. The main objective of this study was to evaluate the usefulness of external audits in the context of implementing new regulations provided by the FMD in the secondary care environment. Methods: The external, in-person workflow audits were performed by an authentication company in three Polish hospital pharmacies. Each audit consisted of a combination of supervision (non-participant observation), secondary data analysis, and expert interviews with the use of an independently designed authorial Diagnostic Questionnaire. The questionnaire included information about ...
Objectives: This study aims to establish expert opinion and potential improvements for the Falsified...
The EU Falsified Medicines Directive (FMD) mandates the serialisation of prescription-only medicines...
Background: Problems with achieving the continuum of medicines management are long-standing. Audits ...
Background: Recently, the European Union has introduced the Falsified Medicines Directive (FMD). Add...
Background: Recently, the European Union has introduced the Falsified Medicines Directive (FMD). Ad...
The Falsified Medicines Directive (FMD) and the Delegated Regulation (DR) will need to be implemente...
Background: The Falsified Medicines Directive (FMD) is a response of the European Union to the incre...
Medical safety through medicine falsifications entering the legal supply chain of medicines have bec...
Objective : The main objective of the prescription audit of the secondary level government hospitals...
Since the publication of the Falsified Medicines Directive in 2011 and the subsequent delegated regu...
OBJECTIVES: Hospital boards are legally responsible for safe healthcare. They need tools to assist t...
Objective: A prescription auditing is a quality improvement or health care improvement process. A pr...
OBJECTIVES:To introduce serialised medicines into an operational hospital dispensary and assess the ...
Objectives: This study aims to establish expert opinion and potential improvements for the Falsified...
OBJECTIVES: To identify the authentication and detection rate of serialised medicines using medicine...
Objectives: This study aims to establish expert opinion and potential improvements for the Falsified...
The EU Falsified Medicines Directive (FMD) mandates the serialisation of prescription-only medicines...
Background: Problems with achieving the continuum of medicines management are long-standing. Audits ...
Background: Recently, the European Union has introduced the Falsified Medicines Directive (FMD). Add...
Background: Recently, the European Union has introduced the Falsified Medicines Directive (FMD). Ad...
The Falsified Medicines Directive (FMD) and the Delegated Regulation (DR) will need to be implemente...
Background: The Falsified Medicines Directive (FMD) is a response of the European Union to the incre...
Medical safety through medicine falsifications entering the legal supply chain of medicines have bec...
Objective : The main objective of the prescription audit of the secondary level government hospitals...
Since the publication of the Falsified Medicines Directive in 2011 and the subsequent delegated regu...
OBJECTIVES: Hospital boards are legally responsible for safe healthcare. They need tools to assist t...
Objective: A prescription auditing is a quality improvement or health care improvement process. A pr...
OBJECTIVES:To introduce serialised medicines into an operational hospital dispensary and assess the ...
Objectives: This study aims to establish expert opinion and potential improvements for the Falsified...
OBJECTIVES: To identify the authentication and detection rate of serialised medicines using medicine...
Objectives: This study aims to establish expert opinion and potential improvements for the Falsified...
The EU Falsified Medicines Directive (FMD) mandates the serialisation of prescription-only medicines...
Background: Problems with achieving the continuum of medicines management are long-standing. Audits ...