Medicines and Healthcare products Regulatory Agency (2024)

Medicines & Healthcare products
Regulatory Agency

  • Alerts, recalls and safety information: medicines and medical devices
  • Drug Safety Update
  • Yellow Card: Report a problem with a medicine or medical device
  • Marketing authorisations and licensing guidance
  • Product information about medicines
  • Medical devices regulation and safety
  • Latest information for patients
  • MHRA guidance on coronavirus (COVID-19)
  • About MHRA
  • All MHRA services and information

Featured

Medicines and medical devices: Five top tips for summer 

Press release

Key advice on medicines and medical devices for the holiday season.

Medicines and Healthcare products Regulatory Agency (1)

MHRA approves Comirnaty JN.1 COVID-19 vaccine for adults and children from infancy

News story

The Medicines and Healthcare products Regulatory Agency (MHRA) has today, 24 July, approved an adapted Pfizer/BioNTech COVID-19 vaccine (Comirnaty) that targets the JN.1 COVID-19 subvariant.

Medicines and Healthcare products Regulatory Agency (2)

Ocrelizumab approved as an injection to treat multiple sclerosis in adults

Press release

The Medicines and Healthcare products Regulatory Agency (MHRA) has approved a new formulation of the medicine ocrelizumab (Ocrevus 920mg solution for injection) to treat relapsing forms of multiple sclerosis (RMS) and primary progressive multiple sclerosis (PPMS) in adults.

Medicines and Healthcare products Regulatory Agency (3)

MHRA approves GLP –1 receptor agonist semaglutide to reduce risk of serious heart problems in obese or overweight adults

Press release

Semaglutide is the first weight loss drug approved in the UK as a preventative treatment for those with established cardiovascular disease

Medicines and Healthcare products Regulatory Agency (4)

MHRA approves the first generic raltegravir medicines to treat adult and paediatric patients infected by HIV

Press release

The Medicines and Healthcare products Regulatory Agency (MHRA) has today, 19 July 2024, approved the first generic raltegravir medicines to treat adult and paediatric HIV patients who weigh at least 40kg.

Medicines and Healthcare products Regulatory Agency (5)

Capivasertib approved to treat patients with advanced breast cancer

Press release

The Medicines and Healthcare products Regulatory Agency (MHRA) has today, 17 July 2024, approved the medicine capivasertib (Truqap) for patients with advanced hormone receptor (HR) positive, human epidermal growth factor receptor 2 (HER2) negative breast cancer which has one or more abnormal “PIK3CA”, “AKT1”, or “PTEN” gene, and does not respond to other anti-hormonal-based therapies.

Medicines and Healthcare products Regulatory Agency (6)

Latest from the Medicines and Healthcare products Regulatory Agency

  • Export medical devices

    • Guidance
  • Register medical devices to place on the market

    • Guidance
  • Access New Active Substance and Biosimilar Work Sharing Initiatives

    • Guidance

See all latest documents

  • Get emails

What we do

The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK.

MHRA is an executive agency, sponsored by the Department of Health and Social Care.

Read more about what we do

Follow us

Documents

Services

  • Report a problem with a medicine or medical device

  • Check drug analysis profiles (iDAPs)

See all services

Guidance and regulation

  • Find product information about medicines

    • Guidance
  • Regulating medical devices in the UK

    • Guidance

See all guidance and regulation

News and communications

  • Medicines and medical devices: Five top tips for summer 

    • Press release
  • MHRA approves Comirnaty JN.1 COVID-19 vaccine for adults and children from infancy

    • News story

See all news and communications

Research and statistics

  • Topiramate: review of safety in pregnancy

    • Research and analysis
  • Digital mental health technology: user and public perspectives

    • Research and analysis

See all research and statistics

Policy papers and consultations

  • Common specification requirements for in vitro diagnostic devices

    • Open consultation
  • Impact of AI on the regulation of medical products

    • Policy paper

See all policy papers and consultations

Transparency and freedom of information releases

  • Human Medicines Regulations 2012 Advisory Bodies Annual Report 2023

    • Corporate report
  • Medicines and Healthcare Products Regulatory Agency Annual Report and Accounts 2023 to 2024

    • Corporate report

See all transparency and freedom of information releases

Our management

Dame June Raine DBE

Chief Executive

Medicines and Healthcare products Regulatory Agency (7)

Amanda Calvert

Interim co-chair

Medicines and Healthcare products Regulatory Agency (8)

Professor Graham Cooke

Interim co-chair

Medicines and Healthcare products Regulatory Agency (9)

Michael Whitehouse OBE

Interim co-chair

Medicines and Healthcare products Regulatory Agency (10)

Liz Booth

Chief People Officer

Medicines and Healthcare products Regulatory Agency (11)

Rose Braithwaite

Chief Finance Officer

Medicines and Healthcare products Regulatory Agency (12)

Dr Alison Cave

Chief Safety Officer

Medicines and Healthcare products Regulatory Agency (13)

Claire Harrison

Chief Digital and Technology Officer

Medicines and Healthcare products Regulatory Agency (14)

Dr Laura Squire OBE

Chief Healthcare Quality & Access Officer

Medicines and Healthcare products Regulatory Agency (15)

Dr Glenn Wells

Chief Partnerships Officer

Medicines and Healthcare products Regulatory Agency (16)

Rachel Bosworth

Director of Communications and Engagement

Mick Foy

Director of Delivery

Carly McGurry

Director of Governance

Nicola Rose

Interim Executive Director, Science and Research

James Pound

Interim Executive Director, Innovation and Compliance

Contact MHRA

General enquiries

MHRA
10 South Colonnade
London
E14 4PU
United Kingdom

Email

info@mhra.gov.uk

Telephone

020 3080 6000

Fax

020 3118 9803

Office hours are Monday to Friday, 9am to 5pm.

Media enquiries

News centre
MHRA
10 South Colonnade
London
E14 4PU
United Kingdom

Email

newscentre@mhra.gov.uk

During office hours:

020 3080 7651 (08:30 - 17:00)

Out of office hours:

07770 446 189 (17:00 - 08:30)

Office hours are Monday to Friday, 8:30am to 5pm. For real-time updates including the latest press releases and news statements, see our Twitter channel at https://www.twitter.com/mhragovuk.

Make an FOI request

  1. Read about the Freedom of Information (FOI) Act and how to make a request.
  2. Check our previous releases to see if we’ve already answered your question.
  3. Make a new request by contacting us using the details below.

Freedom of Information

MHRA Freedom of Information Team
10 South Colonnade
London
E14 4PU
United Kingdom

Email

info@mhra.gov.uk

Corporate information

  • Accessible documents policy
  • Complaints procedure
  • Our energy use
  • Our governance
  • Terms of reference

Jobs and contracts

  • Procurement at MHRA
  • Working for MHRA
  • Jobs

Read our policy on Social media use.

Medicines and Healthcare products Regulatory Agency (2024)
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