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The MHRA ensures that the active ingredients used in all treatments are correctly identified, of high quality, and manufactured to precise specifications.

The MHRA rigorously assesses clinical trial data to ensure the medication effectively treats the condition it is intended for. This guarantees that patients can trust the medication to deliver the intended health benefits.

The manufacturing process is closely monitored to ensure the medication maintains consistency, purity, and stability. This means that every dose of the medication is produced to the same high-quality standard, providing reliable treatment.

The MHRA evaluates safety data from clinical trials and ongoing use to understand potential side effects or adverse reactions. This ensures that the benefits of the treatment outweigh the risks, and helps healthcare professionals make informed decisions when prescribing the medication.

The MHRA verifies that the strength of the medication is appropriate and clearly labeled. This ensures that patients receive the correct dosage necessary for their treatment, promoting safe and effective use.

he MHRA performs a risk-benefit analysis to ensure that the benefits of using a particular medication outweigh any risks associated with its use. By doing so, it ensures that patients receive treatments that significantly contribute to their health while minimising risks.