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Contractors in Britain can turn off their FMD systems after December 31, but the directive will still apply in Northern Ireland for “at least four years”, it has been highlighted.
The UK and EU have agreed a “phased process” for the implementation of medicines regulations in Northern Ireland, to give businesses time to adapt, the government has announced.
The government should implement “robust” plans to ensure patients in Northern Ireland can still access medicines once the Brexit transition period ends, the NPA has said.
The government must put “robust plans” in place to ensure counterfeit medicines don’t enter the supply chain as FMD ceases to apply across the UK post Brexit, the RPS has said.
Proposed legislation to ensure falsified medicines do not enter the UK supply chain risks broadening the use of sensitive data, a Liberal Democrat peer has warned.
The Medicines and Healthcare products Regulatory Agency (MHRA) is investigating circumstances under which multiple medicines left the supply chain before entering it again.
Community pharmacy staff reported shortages across all 30 brands of hormone replacement therapy (HRT) medicines included in a C+D survey between October 2019 and March 2020
The falsified medicines directive (FMD) has reduced manufacturing capacity by 10%, British Generics Manufacturers Association (BGMA) director general Warwick Smith has claimed.