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NHS Litigation Authority

by Jackie (née Heneghan) Peck | Jun 12, 2014 | Behind the scenes, Blog, Community Pharmacy, Pharmacy Brands, Regulation

The NHS Litigation Authority have recently published statistics on their website relating to appeals for pharmacy contracts. The number of appeals since the new market entry regulations has decreased however this may be a market anomaly as applicants get their heads...

Technology in Health and the emergence of Apple

by Jackie (née Heneghan) Peck | Jun 12, 2014 | Behind the scenes, Blog, Regulation

It was announced earlier this month that Apple were launching their own healthcare and fitness app called HealthKit.  The app is part of iOS8 and has the potential to communicate patient health data to hospitals and clinicians. The idea behind all of this is...

Online Pharmacy – are patients better with a ‘face to face’?

by Jackie (née Heneghan) Peck | Jun 12, 2014 | Blog, Community Pharmacy, Pharmacy Brands, Regulation

Recent coverage in the Australian community pharmacy press has centred around the benefit and/or potential harm of prescribing and dispensing medicines without a face-to-face consultation.  The discussion raised asked the question whether an online questionnaire is...

RP & GDP Training for WDA(H)

by Jackie (née Heneghan) Peck | May 12, 2014 | Behind the scenes, Blog, Community Pharmacy, Pharmacy Brands, Pharmacy Suppliers, Regulation

RP – Responsible Person relating to MHRA GDP – Good Distribution Practice – the guidelines by which medicine wholesalers must adhere to WDA(H) – Wholesale Distribution Authorisation for Human Use – previously Wholesale Dealer’s...

Out of Specification (OOS) Test Results

by Jackie (née Heneghan) Peck | May 12, 2014 | Behind the scenes, Blog, Pharmacy Suppliers, Regulation

What are Out of Specification results (OOS)?  It seems to be clear enough in the name but I thought I better check it out. One definition is: All test results which fall outside the specifications or acceptance criteria established in drug applications, drug master...

Quality Agreements- Technical Agreements- Good ones are invaluable!

by Jackie (née Heneghan) Peck | May 12, 2014 | Blog, Pharmacy Brands, Pharmacy Suppliers, Regulation

TAs – when do we need them in place and who with and what should be in them? PCL have been reviewing a few TAs over the last few weeks and we have put a few tips and hints together. If you only follow GDP or GMP; the principals are the same. If you are a...
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Recent Posts

  • MHRA-NICE aligned pathway
  • New regulations for clinical trials
  • Pharmacy Consulting Ltd – Audit Training

Upcoming Courses

  • GDP/RP Cogent Gold Standard Online Training on 14 April 2026
  • Active Pharmaceutical Ingredient (API) and Clinical Trials Online Training on 27 April 2026 2:00 pm
  • Introduction to Good Distribution Practice Online Training on 13 May 2026 10:00 am
  • Superintendent Pharmacist training (Online) on 14 May 2026
  • GDP/RP Cogent Gold Standard Online Training on 19 May 2026

MHRA Alerts & Recalls

Field Safety Notices: 6 to 10 April 2026
13 April 2026
Field Safety Notices: 30 March - 3 April 2026
8 April 2026
MHRA Safety Roundup: March 2026
31 March 2026
Field Safety Notices: 23-27 March 2026
31 March 2026

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