Omnimed complies with the requirements of ISO 13485:2016 [Medical devices | Quality management systems | Requirements for regulatory purposes]. It specifies requirements for a quality management system where an organisation needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. Such organisations can be involved in one or more stages of the life cycle, including design and development, production, storage and distribution, installation, or servicing of a medical device, and design and development or provision of associated activities
As part of our continuous commitment to quality and our ISO accreditation, we value our customers' feedback. We kindly ask that you take a moment to complete our product experience and evaluation surveys to help us continually improve our products and services. We greatly appreciate your participation.
Product Experience survey (1 min)
Product Evaluation survey (5 mins)