MHRA
Medicines and Healthcare products Regulatory Agency
UK regulator for licensed medicines and medical devices. Classifies medicines as POM, P or GSL. Acts on unlicensed medicinal product supply.
MHRA medicines classificationSearch PeptideClear
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Regulatory hub
Five regulators set the rules for peptides, collagen and GLP-1 medicines in the UK. We track what they are saying, in plain English, and link to the primary sources.
Last reviewed . Editorial commentary, not legal advice.
As of July 2026, MHRA regulates licensed UK medicines, including all GLP-1 weight-management medications, which are Prescription Only. That covers the first GLP-1 tablet licensed for weight management, approved on 11 June 2026, which is also prescription-only and cannot be advertised to the public. WADA prohibits most research peptides under S0 or S2 for tested athletes. FDA decisions on Category 1 Bulk Drug Substances are widely cited but not binding in the UK. EMA opinions are typically mirrored by MHRA. ASA enforces the CAP Code on health and weight-loss claims, including the POM advertising ban, which MHRA, ASA and GPhC restated jointly on 18 June 2026.
Each regulator below has a separate remit. We summarise what each one covers, link to our existing deep-dive where it exists, and flag where a deep-dive is still in build.
MHRA
UK regulator for licensed medicines and medical devices. Classifies medicines as POM, P or GSL. Acts on unlicensed medicinal product supply.
MHRA medicines classificationWADA
International anti-doping authority. Publishes the annually-updated Prohibited List. UK Anti-Doping (UKAD) enforces it on tested athletes.
WADA Prohibited List and peptidesFDA
US regulator. Maintains the Category 1 Bulk Drug Substances list under section 503A. The FDA position on a research peptide is widely cited internationally, including by UK media.
Deep-dive coming soonEMA
EU centralised medicines authority. EMA opinions are not directly binding in the UK post-Brexit but are frequently mirrored by MHRA decisions on GLP-1 and peptide medicines.
Deep-dive coming soonASA
UK advertising regulator. Enforces the CAP Code on health and weight-loss claims. POM medications cannot be advertised to the public.
ASA rules on weight-loss advertsLive regulatory tracker
Last updated
Four sentenced to nearly 15 years combined jail time following major MHRA investigation into illegal online supply of medicines
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MHRA grants conditional approval for semaglutide (Wegovy) to treat MASH in adults with moderate to advanced liver fibrosis.
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Semaglutide (Wegovy) approved to treat form of liver disease
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MHRA, ASA and GPhC issue a joint warning on promoting newly licensed prescription-only and unlicensed weight-management medicines.
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Warning on promoting newly licensed prescription-only medicines and unlicensed medicines for weight management
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MHRA approves the first GLP-1 tablet licensed for weight management in the UK. It is prescription-only and cannot be advertised to the public.
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First GLP-1 tablet for weight loss approved in the UK
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Two arrested in the MHRA’s largest ever seizure of unlicensed weight-loss medicines. Around 12,000 doses recovered, including retatrutide, tirzepatide and peptide products.
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High Court orders six UK internet providers to block websites selling counterfeit and unlicensed semaglutide. Extended on 23 Jun 2026 with dynamic blocking.
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MHRA approves a single-dose 7.2mg semaglutide (Wegovy) pen for adults with obesity at a BMI of 30 or above.
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GPhC review of weight-management services reports 1,307 concerns over two years. 27% concerned prescribing practice and 17% advertising.
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MHRA alert on fake Mounjaro (tirzepatide) KwikPen 15mg pens, batch D873576, dispensed by a Birmingham pharmacy. Sterility cannot be confirmed.
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ASA upholds rulings that public discount and referral code posts for online pharmacies advertised prescription-only weight-loss medicines to the public.
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MHRA updates semaglutide product information for the very rare risk of non-arteritic anterior ischaemic optic neuropathy (NAION).
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MHRA updates GLP-1 product information on the small risk of severe acute pancreatitis, after 1,296 Yellow Card reports between 2007 and October 2025.
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MHRA reports seizing almost 20 million doses of illegally traded medicines in 2025, including over 5,000 illegally traded GLP-1 products.
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ASA confirms indirect promotion of weight-loss POMs also breaches the rules, including unbranded pen imagery and terms such as "weight loss jab" and "GLP-1".
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MHRA and Genomics England open the Yellow Card Biobank study into whether genetics influence acute pancreatitis risk from GLP-1 medicines.
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WADA 2025 Prohibited List in force. BPC-157 explicitly named under S0 (non-approved substances).
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FDA Category 1 Bulk Drug Substances list update. Several research peptides remain off the 503A approved list.
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MHRA action on unlicensed semaglutide and tirzepatide supply. Letters issued to UK sellers marketing for weight loss.
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EMA PRAC concludes GLP-1 receptor agonist suicidal ideation signal review. No causal association established.
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ASA and CAP code position: prescription-only medicines including GLP-1 weight-loss drugs such as Wegovy cannot be advertised to the public. The POM advertising ban applies to all paid promotion, including social media.
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PeptideClear maintains these as refreshable datasets rather than one-off articles. Each carries its own source, methodology and last-updated date.
Live data tracker
UK GLP-1 prescribing tracker →
Monthly NHS England primary-care prescribing volumes for GLP-1 medications, rebuilt as each new month publishes. Dated chart, month-by-month table, full methodology.
Source: NHSBSA English Prescribing Dataset
Live data tracker
MHRA enforcement and safety tracker →
Every MHRA safety alert, enforcement action and drug safety update relevant to weight-loss medicines and peptides, dated and linked to the gov.uk original.
Source: gov.uk / MHRA
PeptideClear is editorial. Nothing here replaces the regulator, and you should not take our word for any of it. These are the official UK destinations where the underlying position is published, free to read and open to anyone.
MHRA
MHRA Products portalThe Summary of Product Characteristics and Patient Information Leaflet for every medicine licensed in the UK. This is the authoritative document for what a medicine is licensed to do.
MHRA
Drug Safety UpdateThe MHRA monthly bulletin of safety advice for prescribers and patients. Where new risks and product information changes are formally announced.
MHRA
Report a fake or illegally supplied medicineThe MHRA route for reporting a website or seller supplying medicines illegally, and for reporting a product you believe is counterfeit.
Advertising Standards Authority
CAP Code and ASA rulingsThe UK advertising rules, including the ban on advertising prescription-only medicines to the public, and the published rulings that show how they are applied.
World Anti-Doping Agency
WADA Prohibited ListThe annually updated list of substances and methods banned in sport. Many research peptides sit under S0 or S2. UK Anti-Doping enforces it on tested athletes.
legislation.gov.uk
Human Medicines Regulations 2012The legislation that defines what counts as a medicine in the UK, and what constitutes illegal supply. A product marketed with medicinal claims is regulated as a medicine regardless of how it is labelled.
Dedicated UK regulatory status pages for the most-searched peptides and GLP-1 medicines. Each one summarises the Misuse of Drugs Act position, the Psychoactive Substances Act position, the MHRA marketing authorisation position, the WADA Prohibited List position and the ASA advertising framing.
BPC-157
UK regulatory status
TB-500
UK regulatory status
MOTS-c
UK regulatory status
Ipamorelin
UK regulatory status
CJC-1295
UK regulatory status
GHK-Cu
UK regulatory status
Tirzepatide
UK regulatory status
Semaglutide
UK regulatory status
Liraglutide
UK regulatory status
Retatrutide
UK regulatory status
We pull primary-source statements from MHRA, FDA, WADA, EMA and ASA directly. We do not paraphrase secondary reporting. Where a position has shifted, we date the entry and link to the regulator's own page so the reader can verify. Items still pending source confirmation are held back from the ticker until an editor verifies them against the regulator's own published record.
This page is editorial commentary. It is not legal advice. For binding interpretation of any regulator's position, consult the regulator directly or a qualified UK medicines lawyer.
Related: MHRA medicines classification · WADA Prohibited List and peptides · ASA rules on weight-loss advertising · Research-use-only framing · MHRA Yellow Card scheme.
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