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The MHRA ( Medicines and Healthcare products Regulatory Agency ) has two main application procedures: Simple Reclassification : This is a straightforward and quick procedure based on an analogous product (a medicinal product already on the UK market with the same active ingredient, route of administration, use, and a similar or higher strength/dosage)

Testing: To ensure label accuracy, we prioritized products that are tested throughout the manufacturing process, ideally by third-party labs and organizations, like NSF International

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