HMPWG: Questions and answers document on regulatory and legal issues

HMPWG’s new ‘Questions and answers document on regulatory and legal issues concerning homeopathic medicinal products’ confirms the high legal and regulatory standards for these products within the medicinal products legislation in Europe.

The Homeopathic Medicinal Products Working Group (HMPWG) of the Heads of Medicines Agencies (HMA) has published a ‘Questions and answers document on regulatory and legal issues concerning homeopathic medicinal products in the European framework.’

The document addresses a number of legal and regulatory questions in relation to the EU regulation of homeopathic medicinal products (HMPs) for human and veterinary use. It provides an overview of HMPWG’s position on issues which typically arise in connection with the implementation of the applicable EU rules for these products.

This comprehensive summary of the legal and regulatory framework for our sector confirms the high legal and regulatory standard for homeopathic medicinal products within the medicinal products legislation in Europe.

For further information

• Questions and answers document on regulatory and legal issues concerning homeopathic medicinal products in the European framework