by Jackie (née Heneghan) Peck | Sep 10, 2020 | Blog
In the past, the MHRA has told a pharmaceutical wholesaler to find a new Responsible Person when they did not know the correct definition for “GDP” in their MHRA inspection. The RP used the “ Gross Domestic Product “ definition to his peril…
by Brian Lindsay | Jun 26, 2020 | Blog, MHRA
In its Inspectorate Blog the MHRA published a post on temporary changes in Good Distribution Practice (GDP) entitled “How to manage temporary GDP process changes and risks through the COVID-19 pandemic”…
by Kimberley Peck | Apr 27, 2020 | Blog
The MHRA released guidance on the 9th April for good working practices whilst many of your employees adjust to working from home amid the current climate…
by Adel Nagy | Apr 17, 2020 | Blog
Being a pharmaceutical wholesaler we have to approve/bona fide your suppliers and customers. It is the requirements of Good Distribution Practice (Chapter 5.2. Qualification of suppliers & 5.3. Qualification of customers), the Green Guide book. Performing the verification on your supplier before procuring and on your customer before you can supply products are crucial! Also, only your Responsible Person can approve them, you are not allowed to sell products to unapproved wholesalers. You can get your license suspended if not verifying properly.
by Adel Nagy | Apr 17, 2020 | Blog
We all have expired products, not just as wholesalers but individuals. We buy them as we think we will need it, but some products have short expiry dates, especially cold chain products. As a wholesaler, we have to dispose of damaged or expired stock in accordance with (GDP) Good Distribution Practice – Chapter 5.6. Destruction of obsolete good. The guideline says: