Our chemical analyses for the pharmaceutical industry are carried out in accordance with the European Pharmacopoeia
The European Pharmacopoeia consists of a set of general monographs on the manufacturing of medicines, general analytical methods for substances and medicines, and general formulation requirements (tablets, capsules, injections, etc.) The pharmaceutical sector can also use the analytical methods for products and medicinal products not described in the pharmacopoeia, as well as for the analysis of raw materials used in this sector, cosmetics and food supplements. These quality standards must be met by all medicines sold in the 36 member states of the European Pharmacopoeia to ensure products obtained from pharmacies and other legal suppliers are safe for consumers.
This is why pharmaceutical companies require that control analyses be performed according to the methodologies described in the European Pharmacopoeia documents.