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Do UK MA in the EU have to Serialise the packs for the UK Market when GB does require the packs to be serialised?

Do UK MA in the EU have to Serialise the packs for the UK Market when GB does require the packs to be serialised?

by Jackie (née Heneghan) Peck | Jan 14, 2021 | Blog, FMD

he UK MAs currently cover the whole of the “UK” so the UK MAs include Northern Ireland Supply…

The “Safety features” element of EUFMD (FMD2011/62/EU) and Delegated Regulation (20016/161) What Pharmacies in GB need to know and do?

The “Safety features” element of EUFMD (FMD2011/62/EU) and Delegated Regulation (20016/161) What Pharmacies in GB need to know and do?

by Jackie (née Heneghan) Peck | Jan 14, 2021 | Blog, FMD

Lets start with the definition GB is now only…

The “Safety features” element of EUFMD (FMD2011/62/EU) and Delegated Regulation (20016/161) What Pharmacies in Northern Ireland (NI) need to know and do?

by Jackie (née Heneghan) Peck | Jan 14, 2021 | Blog, FMD

For Northern Irish Pharmacies FMD requirements have not changed and they must continue to verify and decommission their “2D” barcoded packs…

Data Collecting Wearable Devices are helping GPs diagnose and track patient symptoms.

by Jackie (née Heneghan) Peck | Dec 22, 2020 | Blog

On line GP consultations are here to stay for a while and the diagnosis of certain conditions are being aided more and more by wearable devices. Many devices now not only measure (for example) heart rates, they can also track and alert of any irregularities in what...

Updates to the Human Medicines Regulations 2012 to help with Covid 19 Vaccine Temporary Approval

by Jackie (née Heneghan) Peck | Dec 21, 2020 | Uncategorized

In October the  Human Medicines Regulations 2012 were updated to allow the MHRA to grant temporary authorisation of  specific batches of the Pfizer/BioNTech Covid-19 vaccine without needing to wait for EMA approval. The approval is a temporary one which will...
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