EEPI complies with the most advanced international production norms and regulations.

We are dedicated to demonstrating and operating in a quality based environment that complies with international regulations.
Our commitment is supported by ISO and cGMP certifications. Our certificates include:

• ISO 9001:2000 (Quality Management Systems certificate):
• ISO 14001 (Environmental Certification)
• ISO 17025:2005 (Quality Control Laboratories Certification)
• cGMP certification obtained in accordance to the guidelines set by the European Parliament of good manufacturing practices for medicinal products

The Quality Control team employs 80 individuals performing different tasks. At Quality Control, our team of experts is devoted to the examination of products, services and processes for certain minimum levels of quality.
Our objective at Quality Control is to guarantee the Safety and quality of our products, while respecting our cost requirements and conformity with regulatory norms. We achieve this objective through:

• Thorough qualification of raw and packaging materials suppliers to ensure their fulfillment of EEPI requirements and international standards
• Implementation of proper sampling and analytical procedures on starting materials, in-process and finished products
• Implementation of validated analytical methods, covering physical, chemical and microbiological analysis
• Implementation of proper in-process control system on production activities in order to steer the production processes in compliance to predetermined validated specifications

Our objective at Quality Assurance is to make sure that EEPI products are consistently produced and controlled to the Quality standards appropriate to their intended use and as required by the marketing authorization and GMP regulations.
We are able to achieve this objective through:

• Quality Levels Assessments
• Quality Processes Audits
• Supporting operations on any quality difficulties
• Guaranteeing that preventive & corrective measures are identified and well implemented
• Executing Quality action plans and following up through specific performance measurement indicators
• Managing and monitoring Quality related training programs
• Authorizing the final release of products to the market
• Issuing and controlling Quality documentation system (SOPs)