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Medicines regulation

Before they reach the patients who need them, and to ensure their continued safety once in wider use, all medicines, vaccines and medical devices must be strictly regulated by authorities such as the Medicines and Healthcare Products Regulatory Agency (MHRA) and European Medicines Agency (EMA).   

 

The MHRA exists to make sure that medicines, vaccines and medical devices work properly and meet the standards of safety, quality and efficacy. It assesses all new medicines before they can be sold in the UK and continues to monitor the safety of medicines once licensed.

When the MHRA become aware of a potential issue with a medicine or medical device, they will take action to deal with it – this may include alerting healthcare professionals or in some cases withdrawing a medicine from the market.

They also work closely with the European regulator, the European Medicines Agency (EMA), which has a similar role to the MHRA but is responsible for the scientific evaluation, supervision and safety monitoring of human and veterinary medicines in the European Union (EU).

Pharmaceutical companies can submit a single application to the EMA for marketing authorisation in all EU Member States, as well as Iceland, Liechtenstein and Norway.

This is compulsory for some types of medicines, such as for the treatment of HIV/AIDS, cancer, diabetes and viral diseases; advanced-therapy medicines, such as gene-therapy, somatic cell-therapy or tissue-engineered medicines; and medicines used for rare diseases.

Medicines that do not fall within the categories would normally be approved by national agencies like the MHRA.

 

The Yellow Card Scheme

The Yellow Card Scheme is a reporting system which helps the MHRA to monitor the safety of all healthcare products in the UK.

The system is available to individuals and healthcare professionals who wish to report any side effects that may have been caused by a medicine.  

Visit the Yellow Card Scheme website

 

What to do if you experience unexpected side effects

If you are taking or prescribing a medicine and experience any side effects, you should immediately report these to your doctor, to another healthcare professional (such as a nurse or carer) or to the company that produced your medicine.

 

If you have any concerns about a specific Pfizer medication (bearing the Pfizer logo) you can contact Pfizer Medical Information in the United Kingdom on

01304 616161

 

 

PP-PFE-GBR-0576 / Sept 2017