to control the quality of medicines, and the substances used to manufacture them. It is used as an official reference to serve public health. The quality standards of the European Pharmacopoeia apply throughout the entire life-cycle of a product, and become legally binding and mandatory on the same date in all thirty-eight signatory states, which include all the European Union member states.
The European Pharamacopoeia, related to the PET packaging in contact with dry mediines, stablish the raw materials suitable for their manufacturing and the laboratory tests required in order to ensure the eligibility of the raw material used.
SODESA compliance with the European Pharmacopoeia requirements
As shown, we only use materials suitable for the plastic packaging manufacturing for pharmaceutical use and the tests required by accredited laboratories have been done in order to ensure the eligibility of the materials used.