IQS has the certificate of compliance with Good Manufacturing Practices, established in Directive 2003/94/EC, Directive 91/412/EC, which is issued by the Spanish Agency of Medicines and Health Products (AEMPS).
The scope includes the performance of quality control activities (physico-chemical analysis) of active ingredients, medicines and raw materials in general, related to marketed medicines and medicines under investigation.
IQS also has the Certificate issued by the competent authority of the Generalitat de Catalunya.
Likewise, IQS also has the certificate of compliance with the requirements of Part I of the EU Good Manufacturing Practices (GMP) Guidelines issued by Forum Auditorías, which audits our services on behalf of various companies in the pharmaceutical sector.