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Compliance

The quality of our products and the security of our supply chain are critical to our aims, and we take very seriously our responsibility to adhere to all relevant legislation and guidance in this area.

We adhere to the requirements for Manufacture and Importation of Human Medicinal Products as laid down in directive 2001/83/EC and with the principles of Good Manufacturing Practice (GMP) as laid down in EC Directive 2003/94/EC, as amended respectively, and with the principles and practices set down in the current edition of the Rules Governing Medicinal Products in the European Community, Vol IV, Good Manufacturing Practice (GMP) for Medicinal Products.

We also adhere to specific Third Country requirements to support our export activities such as, among others; WHO, Anvisa, and Korean FDA.