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Within the UK and EU, Good Manufacturing Practice (GMP) solely refers to the manufacturing practices within the pharmaceutical industry.

At NHE, we currently operate to GMP standards.

We are working towards obtaining our MIA (Manufacturing / Importers Authorisation) License from the MHRA (Medicine Healthcare Regulatory Authority) in the New Year. Once we have obtained our MIA license we will be certified GMP by UK authorities. As such we will be authorised to manufacture APIs (Active Pharmaceutical Ingredients) on site.

This UK certification is acknowledged worldwide by similar regulatory authorities such as: FDA, EMA (European Medicines Agency) and the TGA (Therapeutic Goods Administration) in Australia.

Producing high quality, pure, natural products
for improving health and well-being