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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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Recent Posts

  • Major Changes to MHRA Medical Device Registration Fees
  • Major Changes to MHRA Medical Device Registration Fees
  • Online Booking Now Available!

Upcoming Courses

  • RP Forum – tbc on 3 February 2026 10:00 am
  • Export Online Training on 4 February 2026 10:00 am
  • Licence Holder Training on 5 February 2026 10:00 am
  • Superintendent Pharmacist training (Online) on 9 February 2026
  • GDP Audit Online Training on 11 February 2026 10:00 am

MHRA Alerts & Recalls

National Patient Safety Alert: Class 1 Medicines Recall Notification: Recall of Quetiapine Oral Suspension (unlicensed medicine), manufactured by Eaststone Limited due to a potential for overdosing, NatPSA/2026/002/MHRA
29 January 2026
Class 4 Medicines Defect Notification: Viatris Products Ltd, Arixtra solution for injection, pre-filled syringes, EL(26)A/04
28 January 2026
Field Safety Notices: 19 to 23 January 2026
27 January 2026
MHRA Safety Roundup: January 2026
27 January 2026

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