How Are Clinical Trials Regulated?

March 25, 2021 4:51 am


The MHRA is responsible for the continual regulation of all clinical trials in the UK. This is to ensure that the substances being tested are safe and effective for use, both in humans and animals. The MRHA regulates all medical devices, pharmaceuticals, cosmetics, drugs, medical research, and more. When looking for a clinical trial, it is important to understand what the purpose of the study is. Some clinical trials will be double blinded, meaning they separate those that are given a placebo from those that are given a real drug. Others are single blinded, meaning they don’t separate the groups. For more details on TQT Studies, visit Richmond Pharmacology

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There are several different types of clinical trials. One is a phase one clinical trial, which generally involves one disease or health condition and a handful of drugs being tested. Phase one trials will not typically provide data on more serious side effects or long term health effects. These trials can be approved and used to aid in the development of treatments for these diseases.

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Other clinical trials involve larger groups, often with more than one drug group. These trials are usually performed on a larger scale than phase one trials and can provide long term data. Long term data is essential in determining how well a new treatment is working. It is also essential in determining whether or not the new drug or treatment is better than the one’s been using previously.