Minimum checks required on medicinal product imported from an *EEA Country by a business in Great Britain (GB)
If your business in GB is looking to import medicinal products from the EEA, there are a number of checks which must be performed by the Responsible Person, prior to release for sale …
This short training video takes you through the preparations for a Good Distribution Practice audit in accordance with EU GDP 2013/C 343/01. It also discusses the key areas to consider when performing the audit and the documents that should be reviewed during the audit.
If you would like more…
Know Your Medicines Supply Chain
When wholesaling in medicines, it is required to purchase, store and distribute medicinal products in such a manner that the quality, safety, identity, purity and efficacy of the pharmaceuticals is not compromised.
The primary concern of the RP is patient s…
Why must Quality Systems be there at the beginning?
Inglasia Pharma Solutions has supported various Pharma/Biotech startups with implementing their Quality Management Systems (QMS). At development and in early stage clinical trials, the QMS have been very much focused on ensuring compliance wi…
Staff training MUST be fit for purpose
This post, previously on LinkedIn, received over 5000 likes!
Placing 10s and 100s of procedures in front of your new starter does not really add any value to the individual, nor the company. These ways of working must change.
Our solution would be to…
The Good Distribution Practice Challenges in Wholesaling & Freight Forwarding of Medicines
The Responsible Person or Responsible Pharmacist, as referred to in some parts of Europe, is the person identified for ensuring the quality and safety of the medicinal product within their supply cha…
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