MHRA Response to contaminated paediatric medicines
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.
What makes a good RP?
What makes a good RP? – The Responsible Person (RP) title is the named person on a Wholesale Distribution Authorisation (WDA).
WDA(H) & Import – New Guidelines:
Following Brexit and GB leaving the EU the MHRA have advised that GB wholesale dealers now need to appoint an RPi
Global crackdown of illicit medicines and medical devices
The MHRA reported today on a global operation which took place at the end of May. See the full report here Co-ordinated by Interpol, the 14th “Operation Pangea” saw over 100 countries joining force. 3 Million illicit medicines were seized valued at £9...
Are you decommissioning products with the correct status?
The EMVO has published a Letter of Announcement on using the correct status when decommissioning pharmaceutical products…
GDP Guidelines : Training to ensure everyone is compliant
It is essential that the whole team understands what those guidelines are and why it is so important to work in them.