Educational materials for health professionals and patients are often required in the Risk Management Plan for a new product and it is a requirement that the UK version must be submitted to the MHRA for review prior to issue. To ensure that your educational material is reviewed by the appropriate assessor within the Agency please submit your documents to
We will acknowledge receipt of your material and provide you with a contact name. A timeline for assessment can be agreed with the assessor and will depend on the urgency with which the materials need to be circulated and other priorities.
Other educational materials not specified in the RMP
Where the materials relate to a new product where the advertising is being vetted, these should be sent to the Advertising Standards Unit in the usual way. Any questions about this can be sent to .