In the vast amount of pharmaceuticals and medical products that are in the marketplace today, guaranteed quality cannot be taken for granted. To make absolutely certain that we deliver high quality products we have an outstanding Quality Assurance policy in place. Imres’s QA process encompasses the complete supply chain; from pre-manufacturing to post delivery.
Our stringent vendor rating system sees Imres visit and screen vendors around the world. Manufacturers must prove that they meet our high, internationally recognised standards, and those of our customers. Our vendors must adhere to the necessary quality control processes. Only after they have passed successfully, will they qualify as an Imres approved vendor or manufacturing facility.
All our products, from pharmaceuticals to medical consumables and medical instruments are subject to our comprehensive qualification process. We have our products tested in WHO pre-qualified and ISO/IEC 17025:2005 certified laboratories. Additionally, GMP audits are being held by our qualified auditors.
At Imres we understand the importance of having our products registered in the countries where they are needed. To this point we have our products registered in more than 20 countries. We constantly focus on both maintaining existing registrations and adding registrations to ensure our products are available for your health programmes.