What does MHRA mean in AGENCIES

The MHRA is the Medicines and Healthcare products Regulatory Agency, a UK-based organization responsible for regulating all medicines and medical devices used in the UK. The MHRA is an executive agency of the Department of Health and Social Care and is responsible for ensuring that all medicines and medical devices meet appropriate standards of safety, quality, and efficacy.

The MHRA's responsibilities include:

• Assessing and authorizing all new medicines and medical devices for use in the UK
• Monitoring the safety of medicines and medical devices once they are on the market
• Taking action to protect public health if a medicine or medical device is found to be unsafe or ineffective
• Providing information and advice to the public and healthcare professionals about medicines and medical devices

The MHRA assesses new medicines and medical devices through a rigorous scientific review process. This process involves evaluating the results of clinical trials and other scientific data to determine whether the medicine or medical device is safe and effective. The MHRA also considers the potential risks and benefits of the medicine or medical device and whether it meets appropriate standards of quality.

The MHRA monitors the safety of medicines and medical devices once they are on the market through a variety of mechanisms, including:

• Receiving and investigating reports of adverse events from healthcare professionals and patients
• Conducting inspections of manufacturers and distributors
• Reviewing scientific literature and other sources of information
• Taking action to address any safety concerns that are identified

If you have a concern about a medicine or medical device, you should contact your doctor or pharmacist. You can also report the concern to the MHRA by visiting their website or calling their helpline.