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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...

Patient Compliance and Augmented Reality “AR”

by Jackie (née Heneghan) Peck | Dec 20, 2020 | Blog

Augmented Reality is being used as a tool to aid patient compliance. Smart phones, apps, cameras  and tablets help to improve patient information and confidence with their medicines. Silver surfers are much more tech savvy.
Artificial Intelligence (AI) and the development of new Covid-19 treatments

Artificial Intelligence (AI) and the development of new Covid-19 treatments

by Jackie (née Heneghan) Peck | Dec 19, 2020 | Blog, Covid 19

The use of innovative technologies like Artificial Intelligence (AI) has been invaluable in a lot of the research being carried out during the Coronavirus pandemic. Algorithms which examine the relationships between disease and existing drugs can crunch data quickly....

The True Cost of Brexit to the UK public

by Jackie (née Heneghan) Peck | Dec 17, 2020 | Blog, Brexit, FMD

The Pharmaceutical Industry in the UK has been hit by the massive increase in the cost of Regulatory Changes. The pharmacy companies in the UK may suffer with the loss of EU collaborative research. There is uncertainty what the effect on no MRA and no FMD will be in...
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Recent Posts

  • Medical Devices: Conformity Assessment and the UKCA Mark
  • Are Audit clip boards and checklists obsolete?
  • Major Changes to MHRA Medical Device Registration Fees

Upcoming Courses

  • GDP Audit Online Training on 9 March 2026 10:00 am
  • Export Online Training on 12 March 2026 10:00 am
  • Understanding GPhC Guidance for Online Pharmacies – Online Training on 16 March 2026
  • GDP/RP Cogent Gold Standard Online Training on 17 March 2026
  • GDP/RP Cogent Gold Standard WEEKEND Training on 20 March 2026 9:30 am

MHRA Alerts & Recalls

MHRA Safety Roundup: February 2026
25 February 2026
Class 4 Medicines Defect Notification: Rayner Pharmaceuticals Limited, Dropodex 0.1% w/v Eye Drops, solution, EL(26)A/10
24 February 2026
Field Safety Notices: 16-20 February 2026
24 February 2026
Class 2 Medicines Recall: Sterling Pharmaceuticals Ltd (specials manufacturer MS 32515), KidNaps (Melatonin) 1mg in 1ml Oral Solution, EL(26)A/09
23 February 2026

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