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Medicines and Healthcare products Regulatory Agency

Medicines and Healthcare products Regulatory Agency

The Medicines and Healthcare products Regulatory Agency (MHRA) is a UK government agency responsible for ensuring that medicines, medical devices, and blood components for transfusion meet applicable standards of safety, quality, and efficacy.

Communication Overview

Total releases

Number of press releases published by this department during the last 12 months, based on publicly available announcements.
743

Avg per month

Average number of press releases published per calendar month over the last 12 months. This smooths short-term fluctuations in publishing activity.
12.4

Avg word count

Average length of published press releases, measured in words. Calculated only for months where content was published.
872

Avg readability

Average Flesch Reading Ease score across all published press releases. Higher values indicate plainer English. Scores are indicative only and vary by subject matter.
26.7

Friday PM releases

Percentage of press releases published after 3pm on Fridays, relative to the department’s total output during the period.
4.1%

Single-release items

Estimated proportion of announcements published once, without a closely related follow-up release during the same period. This is based on similarity of titles and timing.
100%
Metrics are descriptive only and indicate publication patterns rather than intent or impact.

Releases per month

Based on publicly published press releases (last 12 months)

851 articles

Showing 1-30

Two arrested during the MHRA’s largest ever seizure of unlicensed weight loss medicines 

Two arrested during the MHRA’s largest ever seizure of unlicensed weight loss medicines 

Friday, 29 May 2026

The raid on a Northamptonshire estate dismantled what is believed to be a major illicit manufacturing and distribution operation...

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Rilzabrutinib authorised to treat adults with immune thrombocytopenia when prior treatments have been insufficient 

Rilzabrutinib authorised to treat adults with immune thrombocytopenia when prior treatments have been insufficient 

Friday, 29 May 2026

As with any medicine, the MHRA will keep the safety and effectiveness of rilzabrutinib under close review. ...

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Precautionary recall of blood pressure medication (Crescent Pharma Limited Ramipril 2.5mg capsules) after packaging error

Precautionary recall of blood pressure medication (Crescent Pharma Limited Ramipril 2.5mg capsules) after packaging error

Thursday, 28 May 2026

Patients taking Crescent Pharma Limited Ramipril 2.5mg capsules are advised to check their packaging for batch number GR155023 and contact their pharm...

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MHRA welcomes Jason Bonander as he starts his role as Chief Digital and Technology Officer

MHRA welcomes Jason Bonander as he starts his role as Chief Digital and Technology Officer

Wednesday, 27 May 2026

Jason is an experienced technology leader with over 25 years working in tech leadership and health informatics. ...

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Don’t let this heatwave affect your medicines: Three important tips from the MHRA

Don’t let this heatwave affect your medicines: Three important tips from the MHRA

Tuesday, 26 May 2026

Essential advice on protecting your medicines during extreme heat and staying safe. ...

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Landmark new plans bring treatments for rare diseases a step closer

Landmark new plans bring treatments for rare diseases a step closer

Wednesday, 20 May 2026

The MHRA launches public consultation on new framework that could lead to earlier licensing for therapies for up to 3.5 million people in the UK....

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MHRA consults on new regulatory framework to make UK a global leader in rare disease therapy development 

MHRA consults on new regulatory framework to make UK a global leader in rare disease therapy development 

Wednesday, 20 May 2026

Proposed Rare Disease Therapies Framework introduces Investigational Marketing Authorisation and compressed development pathways – industry urged to r...

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MHRA  to support local life sciences sector in Wales

MHRA to support local life sciences sector in Wales

Tuesday, 19 May 2026

MHRA announces new programme of events and greater engagement with industries, researchers, local NHS and government in Wales. ...

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Professor Joann Rhodes: The Rules Need to Bend – Why Flexible Policies and Real Partnership are the Keys to unlocking Life Sciences Potential

Professor Joann Rhodes: The Rules Need to Bend – Why Flexible Policies and Real Partnership are the Keys to unlocking Life Sciences Potential

Monday, 18 May 2026

Innovation doesn’t wait for the rules to catch up. The question is whether we can build a system agile and flexible enough to keep pace....

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MHRA approves beremagene geperpavec (Vyjuvek) for the treatment of dystrophic epidermolysis bullosa

MHRA approves beremagene geperpavec (Vyjuvek) for the treatment of dystrophic epidermolysis bullosa

Friday, 15 May 2026

As with any medicine, the MHRA will keep the safety and effectiveness of Vyjuvek under close review. ...

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MHRA supports Northern Ireland life sciences sector with new hub

MHRA supports Northern Ireland life sciences sector with new hub

Wednesday, 13 May 2026

The MHRA hub in Belfast will strengthen collaboration and engagement with local industry, academia and the healthcare sector. ...

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MHRA strengthens safety warnings for finasteride and dutasteride

MHRA strengthens safety warnings for finasteride and dutasteride

Monday, 11 May 2026

Updated safety advice has been issued to strengthen warnings about potential psychiatric and sexual dysfunction linked to finasteride and to provide p...

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MHRA opens UK wide consultation on redefining gene therapies

MHRA opens UK wide consultation on redefining gene therapies

Monday, 11 May 2026

To future-proof the sector and ensure regulation keeps up with scientific and technological developments, the MHRA is consulting on proposed changes t...

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MHRA invites views on proposed changes to medical device regulation

MHRA invites views on proposed changes to medical device regulation

Monday, 11 May 2026

New pre-market regulatory requirements for medical devices and in vitro diagnostic devices entering the GB market have been published....

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MHRA delivers its targets to increase access to medicines and reinforce UK position as a global destination for life sciences

MHRA delivers its targets to increase access to medicines and reinforce UK position as a global destination for life sciences

Friday, 08 May 2026

The MHRA continues to speed up access to medicines for patients, increase efficiency of regulation and help to attract innovation and investment in th...

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MHRA approves donidalorsen (Dawnzera) for the treatment of familial chylomicronemia syndrome

MHRA approves donidalorsen (Dawnzera) for the treatment of familial chylomicronemia syndrome

Thursday, 07 May 2026

MHRA approves donidalorsen (Dawnzera) for the treatment of familial chylomicronemia syndrome ...

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MHRA approves donidalorsen (Dawnzera) for the treatment of hereditary angioedema

MHRA approves donidalorsen (Dawnzera) for the treatment of hereditary angioedema

Thursday, 07 May 2026

MHRA approves donidalorsen (Dawnzera) for the treatment of hereditary angioedema...

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Operation Pangea XVIII: UK Border operation intercepts millions of dangerous medicines across two weeks

Operation Pangea XVIII: UK Border operation intercepts millions of dangerous medicines across two weeks

Thursday, 07 May 2026

MHRA and UK Border Force crack down on the illegal medicines trade in intensive 14-day international operation. ...

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MHRA approves Linerixibat (Lynavoy) for the treatment of itch due to biliary tract disease

MHRA approves Linerixibat (Lynavoy) for the treatment of itch due to biliary tract disease

Friday, 01 May 2026

As with all medicines, we will continue to closely monitor the safety and effectiveness of linerixibat as it is used more widely....

Read More → press_release
Recommended use of some nasal decongestant sprays limited to five days by UK regulator

Recommended use of some nasal decongestant sprays limited to five days by UK regulator

Thursday, 30 April 2026

The MHRA has limited the use of nasal decongestant sprays containing xylometazoline and oxymetazoline to a maximum of five days due to side effects of...

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MHRA hires top global tech talent to transform systems behind regulation of medicines and medical devices

MHRA hires top global tech talent to transform systems behind regulation of medicines and medical devices

Wednesday, 29 April 2026

The Medicines and Healthcare products Regulatory Agency (MHRA) is pleased to announce the appointment of Jason Bonander as its new Chief Digital and T...

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Seven sentenced after MHRA investigation uncovers £1.8m illegal medicines and steroids network

Seven sentenced after MHRA investigation uncovers £1.8m illegal medicines and steroids network

Wednesday, 29 April 2026

An MHRA-led investigation has exposed a £1.8 million illegal medicines and steroids network, leading to seven men being sentenced....

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Precautionary?recall of antidepressant medication due to manufacturing error

Precautionary?recall of antidepressant medication due to manufacturing error

Tuesday, 28 April 2026

The MHRA?has?advised healthcare professionals to?stop supplying the affected?batch of Sertraline 100mg?and?return all remaining stock to their supplie...

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Launch of clinical trial reforms

Launch of clinical trial reforms

Monday, 27 April 2026

Patients in the UK to get access to new treatments faster and still safely under new clinical trial regulations coming into force on 28 April 2026....

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Precautionary recall of medication used for pain and inflammation?due to incomplete patient information

Precautionary recall of medication used for pain and inflammation?due to incomplete patient information

Thursday, 23 April 2026

Specific batches of Napralief 250mg Gastro?Resistant Tablets are being recalled because important safety and dosage information is missing from both t...

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Enflonsia (clesrovimab cfor) approved to prevent RSV in newborns and infants

Enflonsia (clesrovimab cfor) approved to prevent RSV in newborns and infants

Wednesday, 22 April 2026

As with any medicine, the MHRA will keep the safety and effectiveness of Enflonsia under close review....

Read More → press_release
Precautionary recall of blood pressure medication after manufacturing error

Precautionary recall of blood pressure medication after manufacturing error

Monday, 20 April 2026

The MHRA?has?advised pharmacy and healthcare professionals to stop supplying the impacted batch and?return all remaining stock to their suppliers....

Read More → press_release
How to seize the growing opportunities of AI and technology ahead

How to seize the growing opportunities of AI and technology ahead

Wednesday, 15 April 2026

By Dame Jennifer Dixon...

Read More → news_story
Single dose 7.2mg semaglutide (Wegovy) pen approved to treat adult patients with obesity

Single dose 7.2mg semaglutide (Wegovy) pen approved to treat adult patients with obesity

Tuesday, 14 April 2026

As with any medicine, the MHRA will keep the safety and effectiveness of Wegovy under close review....

Read More → news_story
MHRA and eBay working in partnership to safeguard public health

MHRA and eBay working in partnership to safeguard public health

Monday, 13 April 2026

MHRA and eBay partnership removes 215 listings of potentially dangerous medicines from the eBay platform highlighting the benefits of private/public w...

Read More → press_release

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