Following the introduction of the European Traditional Herbal Medicinal Products Directive (THMPD) 2004/24/EC on 30 April 2011, which mandated the implementation of traditional herbal registration schemes within the EU member states for those herbal medicines suitable for use without medical supervision, there has been need for manufacturers to obtain either a full MA based on the safety, quality and efficacy of the product, or a traditional herbal registration (THR) based on the safety, quality and evidence of traditional use of the product.

SKS has experience in these registration procedures and can assist with provision of expert advice and guidance in the preparation of THRs or MAs.

Contact us for more information.