Guidance

Early Access to Medicines Scheme - Overview

Updated 8 April 2025

1. Overview

The Early Access to Medicines Scheme (EAMS) aims to give patients with life threatening or seriously debilitating conditions access to medicines that do not yet have a marketing authorisation when there is a clear unmet medical need (new medicines and new uses [indications] for established medicines). Under the scheme, the Medicines and Healthcare products Regulatory Agency (MHRA) will issue a scientific opinion on the benefit/risk balance of the medicine, based on the data available when the EAMS submission was made.  Patient access is provided after a 2-step evaluation process:

*the Promising Innovative Medicine (PIM) designation *the Early Access to Medicines Scheme Scientific Opinion

The scientific opinion supports prescribing of the EAMS medicine by the Healthcare Professional; in turn, the EAMS medicine is made available by the EAMS Scientific Opinion holder (usually a pharmaceutical company). The scientific opinion lasts up to a year and can be renewed. The scheme is voluntary and the scientific opinion from the MHRA does not replace the normal licensing procedures for medicines.

Comprehensive information for applications is published in our guidance Early Access to Medicines Scheme - Information for Applicants.

2. Fees

For fees please see MHRA fees.

3. Dates for submission, Day 1 and Day 45

You need to make your EAMS scientific opinion submission by one of the dates below:

Submission Date Day 1 Day 45
28 April 2025 5 May 2025 18 June 2025
26 May 2025 2 June 2025 16 July 2025
23 June 2025 30 June 2025 13 August 2025
21 July 2025 28 July 2025 10 September 2025
18 August 2025 25 August 2025 8 October 2025
15 September 2025 22 September 2025 5 November 2025
13 October 2025 20 October 2025 3 December 2025
10 November 2025 17 November 2025 31 December 2025
8 December 2025 15 December 2025 28 January 2026

4. EAMS applications: pending, refused, granted

View the number of EAMS applications pending, refused and granted.

View current scientific opinions, including public assessment reports and EAMS treatment protocols.

View expired scientific opinions.

5. EAMS task group and principles guidance

A government - industry stakeholder task group has produced additional EAMS guidance, including UK wide core principles

Definitions:

*The Early Access to Medicines Scheme means the scheme of that name established and operated under regulation 167C(1) of The Human Medicines Regulations (2012)

The Human Medicines (Amendments Relating to the Early Access to Medicines Scheme) Regulations 2022 (legislation.gov.uk)

*EAMS medicinal product means a medicinal product that has been included in the Early Access to Medicines Scheme by means of the licensing authority issuing an EAMS scientific opinion *EAMS Scientific Opinion holder means the holder of an EAMS scientific opinion, and accordingly, is the person who places on the market the product to which the opinion relates

Contact: please contact our EAMS coordinator for help and queries:

EAMS@mhra.gov.uk