I remember first hearing about the shared commitment to public involvement when it was announced. I was working in a research department of a hospital, experiencing first-hand how people’s lived experience could drive more inclusive and meaningful health and social …
In this blog we describe ways to facilitate the review of your initial application, how to avoid unnecessary amendments and, where substantial amendments are necessary, how to submit these so that the review is as efficient as possible, leading to …
The Information Processing Unit (IPU) is a part of the Information Management Division at MHRA. As the main submission hub for the Agency, in IPU we are responsible for making sure regulatory applications relating to Marketing Authorisations and Clinical Trial …
Since its launch in 2012 MHRA's Innovation Office has proved a popular resource with not-for-profit organisations and companies alike. We offer a free and confidential regulatory advice service that is tailored to the needs of each individual who contacts us …
The Regulatory Information Service (RIS) was formed in 2006 to act as a main point of contact for industry and their representatives for a range of enquiries - from simple administrative queries right through to complex regulatory queries - and …