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Selection during the analytical development phase of the most adequate analytical method of control quality of the product according to synthetic route used, and detect and quatify potential theoretical impurities.
Our Quality Assurance system has been designed and built up to provide HIGH LEVEL OF CONSISTENCY IN QUALITY including but not limited to change control, personnal trainings, OOS and deviations investigations, maintenance program.
INTEROR quality policy relies on shared value of :
Our efficient quality control department
has a double aim :
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Our engineers and well trained technicians assure also the routine quality control production needs.
INTEROR, as an actor of the pharmaceutical supply chain, is regularly inspected by the ANSM (French Health Authority), holds a cGMP certificate downloadable on EudraGMP website, and GMP+ certificate.
This Quality Assurance System is based on cGMP principles (ICHQ7) with graduated implementation to our productions and a full enforcement to our Active Substance and cGMP intermediates productions.
INTEROR keeps developping a large products portfolio from starting materials to regulatory starting materials and GMP
products. Today, our quality department employs PEOPLE,
IN QUALITY CONTROL AND IN QUALITY ASSURANCE.
MODERN EQUIPMENT AND TECHNIQUES (GC, HPLC, Head space...) are used under good manufacturing practice, and are data integrity compliant.