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Dermal fillers may become Prescription Only – What do you think ?

by Jackie (née Heneghan) Peck | Jul 24, 2017 | Blog

The Nuffield Council on Bioethics recommends that dermal fillers become prescription only. This would mean that they would not be able to be advertised in line with other prescription only medicines. Currently many prescribers order their fillers on prescription,...

Clean Backups, Robust Firewalls, Patch Updates, tightly managed passwords, and access privileges, do you have all of these?

by Jackie (née Heneghan) Peck | Jul 24, 2017 | Blog

The MHRA have been issuing majors to pharmaceutical wholesalers for several years if they do not have a backup procedure and there is no evidence of it being tested. Loss of data may result in a critical finding if it cannot be produced during an inspection. Why do...

Is your medical equipment vulnerable to a cyberattack? You better find out.

by Jackie (née Heneghan) Peck | Jul 24, 2017 | Blog

Is the software embedded in your medical equipment vulnerable to a cyberattack? Equipment running older software is much more vulnerable to cyberattack. Older software may be embedded in medical devices and may require regular updates. Find out if it is possible?...

Seven useful terms explained for new wholesalers who want to Export medicines out of the EEA.

by Jackie (née Heneghan) Peck | Jun 21, 2017 | Blog, Export Training, Training

Seven useful terms: “IATA” “The International Air Transport Association “this body regulates air travel worldwide. IATA are responsible for security and safety of air travel and the regulation of air transport of dangerous goods. “CEIV “Centre of Excellence for...

Contracting a Consultant is only half the battle!

by Jackie (née Heneghan) Peck | Jun 21, 2017 | Blog, Consultancy

Quality Management Systems (QMS) for Wholesalers can be built by a consultant alone, but the best QMS is one which has input from the Company, the staff who carry out the activities and the managers who are responsible for the business and specific processes within...

Centrally authorised Medicinal Products for Human and Veterinary Use

by Jackie (née Heneghan) Peck | May 23, 2017 | Blog, Brexit, Good Distribution Practice - GDP, WDA(H)

The UK triggered Article 50 of the Treaty on European Union on 29th of March 2017 and as a result all primary and secondary law ceases to apply to the UK from 30th of March 2019. Companies who hold centrally authorised “MA s” must proactively review their MA terms,...
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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

Field Safety Notices: 23-27 February 2026
3 March 2026
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

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Wellesley House
10 Eelmoor Road
Farnborough
Hampshire
GU14 7QN

Phone: 01252 375362
Email: [email protected]
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