| In accordance with directive 2003/94/EC of the European Parliament, all medicinal products manufactured outside the EU, if intended for sale within the EU, must be certified by a Qualified Person (QP) prior to their release onto the market. Whether you have a requirement for products manufactured outside of the EU to be imported, tested or QP released, Millmount Healthcare can cater to your individual needs. For more information on any of the Regulatory or Quality services provided by Millmount Healthcare, contact us today! |






