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Falsified Medicines Directive in a Secondary Care Environment-Impact on Supply Chain.

Piotr MerksUrszula ReligioniNuno Pinto de CastroAnna AugustynowiczKatarzyna Plagens-RotmanDavid BrindleyAnna KowalczukJustyna KaźmierczakAgnieszka Neumann-PodczaskaEliza BlicharskaKatarina Fehir ŠolaMartin J HugKlaudiusz GajewskiPaweł Piątkiewicz
Published in: International journal of environmental research and public health (2022)
The Falsified Medicines Directive (FMD) and the Delegated Regulation (DR) impact the pharmaceutical supply chain. Ahead of the deadline for implementation, in February 2019, every entity of the supply chain had to adapt its operations to the regulatory requirements to be compliant with the directive. This paper analyzes the supply chain of a hospital pharmacy and the impact of the FMD implementation. Furthermore, a cost analysis was performed demonstrating that the FMD increases expenditure in the secondary care environment dispensing operations. Governments should be aware that this regulation will certainly impact public healthcare institutions in the long term.
Keyphrases
  • healthcare
  • quality improvement
  • primary care
  • transcription factor
  • affordable care act
  • health information
  • health insurance
  • acute care