Controlled Drug Requirments; If you are a wholesaler, licensed to sell controlled drugs, and you sell schedule 2 or 3 controlled drugs to medical or dental practices in the community, each order must be accompanied by a Controlled Drug requisition (FP10CDF in England). There are two common points of misunderstanding in relation to these forms and their use:
COSHH – All businesses must be aware of and take appropriate actions in relation to their responsibilities under COSHH.
Another Medical Device update. The MHRA will shortly be opening a public consultation on the future direction of Medical Device regulation, it is vital that all relevant voices are heard so please monitor the MHRA notices and respond when appropriate.
Deadline approaching – Medical Device Registration for registering Class IIa and Class IIb (other than implants) products with the MHRA is the end of August 2021.
There is much discussion at all levels at the moment about the Withdrawal…
