Most of us rely on medication to perform functions that our body cannot to relieve pain. We trust the instructions given and know that even though we consume medication at our own risk, it has undergone extensive clinical research been tested and regulated. Medical regulation is vital as without it, taking medication would be a lot more dangerous. Medical safety regulations in the UK is currently the responsibility of the Medicines and Healthcare Products Regulatory Agency (MHRA), previously it was the job of the Department of Health to ensure the safety of medicine that was sold to millions of people every day.44

The MHRA is a government run company that ensures safety through medical regulation and makes sure that all medicines and medical devices bought and used by the public work properly comply to international standards. Stringent regulations ensure that all safety measures are met and that all medicines and medical devices serve their purpose. The MHRA believes that they will be able to spot any medical products and devices that do not meet the highest standards or are faulty for any reason.

As well as keeping a watchful eye over the medical industry and the production of medicinal products, the MHRA hopes to provide greater access to certain products that haven’t always been accessible to all people in the UK. In doing this, the MHRA hopes that all advanced technology and new medical developments will be available to the public.

Medical regulation is imperative as all products should be tested and retested before being sold to the public. According to the MHRA, medicinal products can never claim that they are 100% safe, because all medicines have side effects, whether they are minor or major. As we know, everyone is different and this results in everyone having different side effects to various products.

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