The UK regulator for medicines, medical devices and blood components for transfusion in the UK, The Medicines and Healthcare products Regulatory Agency (MHRA) have further extended the validity period of Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP) Certificates.
Good Distribution Practice applies to the whole business, so if you have a WDA, one of the requirements is that you work to GDP. As part of your licence terms, it is the responsibility of the RP to ensure that all staff involved in GDP activity are trained in GDP.
Anyone who has recently reviewed the Medicines and Healthcare products Regulatory Agency (MHRA) CMS may have noticed the notification at the bottom of the search page regarding GMP and GDP Certificates, stating the following
On the 7th of October The Medicines and Healthcare products Regulatory Agency (MHRA) released a response to contaminated paediatric medicines identified by the WHO region of Africa.
Temperature controlled transport, are you transporting Pharmaceuticals correctly? This is a hot topic right now, especially with the unprecedented weather we have begun to experience lately.
An Introduced Product is an unlicensed medicine which can be imported from a country other than an approved country for import to be exported to a country other than an approved country for import, or if imported from a non-EEA country into Northern Ireland for export back to a country outside the EEA.
