We at George Philips are committed to provide the highest quality of medical disposables that not only meet but exceed our customer’s requirements and expectations.
We have developed, documented, implemented, maintained and are continually improving our Quality Management System to ensure compliance with national and international quality systems standards and regulations. Our Quality Systems, Quality Test Plans and Quality Procedures ensure that our focus is always on continuous monitoring, measurement and improvement of our core process to ensure effectiveness of high quality and efficiency.
All our products are 100% tested and run through a barrage of tests before it is ready to be released into the market. Various tests are carried out through the different stages of the manufacturing processes, including in-process, process validations, until the final product is packed, sterilized & validated for sterility.
All our products are designed and manufactured to meet the requirements of relevant ISO and EN standards. We have been accredited with the following Quality Certifications: CE, ISO 13485, ISO 9001, FDA (Schedule M), WHO GMP, US FDA (Facility Registration), ISO 14001, OSHAS 18001.
We employ Good Manufacturing Practices throughout every stage of the manufacturing process and continue to invest in state-of-the-art engineering and technological resources to ensure consistency in product quality.