Quality Control Area (QC)

QC uses 25% of the manpower of the Company. It follows analytical methods required by both the United States Pharmacopeia (USP) and the European Pharmacopeia (EP), and applies quality standards established by both Pharmacopeias. It has modern equipment operated by highly qualified personnel.

Quality Control objectives are:
• Quality control of the raw materials, intermediates and finished products.
• Development of analytical methods.
• Development of analytical standards.

Quality Assurance Area (QA)

As quality standards are more demanding every day, particularly for pharmaceutical companies, ERIOCHEM has a Quality Assurance Area. It is Quality Assurance’s responsibility to ensure that all GMP regulations are followed. This is achieved by means of a strict control of all processes, documentation and personnel which is verified periodically with internal and external audits. Quality Assurance also has responsibilities on the documentation files of the plant, on the activities related with validation and equipment calibration, and on all aspects tied to hygiene and work safety.