In order to ensure the quality of our innovative devices for the Medical Community we have a formal Quality management system which is certified to the requirements of ISO13485:2016. Every Welfare Medical product is CE marked. We are committed to maintaining a quality system that provides for safe and effective products and services that meet the needs and requirements of our customers. We are proud to cooperate with TÜV SÜD as our Notified Body
As part of a dedication to excellence Welfare Medical Ltd. is committed to the consistent supply of high quality medical products, to innovative designs, which provide outstanding value to the users.
The company shall comply with the requirements of EN ISO 13485:2016, European Council Directive 93/42/EEC of June 1993 concerning Medical Devices and the subsequent revisions described in Council Directive 2007/47/EC, in order to establish, maintain and continually improve the effectiveness of the Quality Management System.
Management will strive to attain and maintain the highest possible standards of quality and service in order to meet or exceed customer expectations. It is the company policy to:
- Keep & maintain records of the quality management system in accordance with current required standards, regulations and directives.
- Ensure those involved are trained, and conversant in their role within the quality management system, so that the company consistently supplies quality products and good customer service.
- Develop or acquire products which are effective, safe & reliable.
- Strive for continual improvement in performance through internal and external communications.