Pharmaceutical approval for ENTONOX
ENTONOX, in common with other medical gases, is essential to modern medicine and should be considered, prescribed and administered with the same precision and care as any other pharmaceutical.
The products from BOC Healthcare satisfy the strict requirements stipulated by the European legislation and are licensed for medicinal use by the Medicines and Healthcare products Regulatory Agency (MHRA). BOC was the first company to have a Marketing Authorisation for Entonox, made under the strict standards required for the manufacture of pharmaceutical gases. In addition to the requirements for operating to a Quality Management System compliant with the requirements of the EC GMP Guide, the guidelines include detailed requirements for personnel, training, premises and equipment, documentation, production, quality control, storage and release (specifically detailed for medicinal gases through Annex 6 of the European Guide for GMP).
Therefore, with ENTONOX, BOC Healthcare can offer to both patients and healthcare professionals a safe, reliable and simple application, meeting all the quality criteria of a registered pharmaceutical.
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