InQpharm is dedicated to providing the highest quality standards throughout its organisation so that our compounds and products are regulated and safe. We ensure that our manufacturers, researchers and distribution partners embrace our quality policies and can meet the stringent quality standards required for the manufacturing of medical devices.
Our business has been certified to meet the quality standard EN ISO 9001:2008 and we are certified as a medical device manufacturer meeting the quality standard EN ISO 13485:2003 by TUV Rheinland in Germany.
The quality management team at our headquarters regulates all our processes, raw material production, manufacturing and distribution to ensure that all quality systems are up to date and continually improving. We ensure that our manufacturers comply with our total quality management systems and that they comply with EN ISO 9001, ISO 13485, Good Manufacturing Practices (GMP) and FDA guidelines. They are also required to meet the requirements of the countries’ regulatory agencies, such as the US FDA guidelines and the highly recognised voluntary standards of organisations such as the International Food Standards Agency (IFS).
Our quality policy ensures that we manage our external suppliers and contract manufacturers through documentation systems, certification and compliance. We have an effective product quality and supplier management control system which ensures that products meet our standards and provide a high level of customer satisfaction. We continually audit, regulate and control our quality levels to deliver a high customer satisfaction rating and we include this as one of our core values to deliver excellence whilst striving for continuous improvement.