We’ve carefully designed a highly flexible quality framework to meet ISO9001:2008 standards, ensuring that we’re exceeding expectations for performance and results without placing any constraints on the innovation and creativity that’s essential to the ide development process
Carrying out all projects within the ide QMS, we will deliver:
- High quality products and services that meet our clients’ expectations
- Products that meet the needs of the market and realise their commercial potential
- Achievement of agreed quality and performance objectives, including budgets and deadlines
- Responsible and safe conduct with the surrounding environment
Quality to match medical industry standards
Thanks to our extensive experience in design for medical
devices, ide also have a complete grasp of ISO13485 regulatory
environments. We can produce documentation required by the European
Union, US Food and Drug Administration (FDA) and other bodies to get
medical products approved and can manage the regulatory process as
required. By offering our clients design control procedures that are
ISO13485 compliant, we’re making sure that all risks and quality issues
are managed and minimised.