We continue our efforts by developing innovative products and dedicating ourselves to quality management of our products, procedures, and suppliers, to prevent injuries for all sharps users around the world. We have developed a wide range of safety solutions for sharps management and medication labelling.
We also recognise that workplace safety goes beyond the use of safety devices. As part of our commitment to improve workplace safety, we are active at advocating staff safety at the industry and regulatory levels. Education programs are regularly conducted to raise awareness of sharps injuries and workplace safety. We also vigorously advocate legislative change to integrate staff safety audits into the current independent accreditation programs for hospitals in Australia, the United States, the United Kingdom, Europe, and Asia.
We are committed to fulfilling customer satisfaction and regulatory requirements through quality management systems for continued improvement of our products and services. Qlicksmart is accredited to ISO 13485, the International Standard for Quality Management System for medical device companies. In particular, our quality system complies with:
- FDA 21 CFR Part 820
- EC Council Directive 93/42/EEC as amended by Directive 2007/47/EC
- Australian Therapeutic Goods Act 1989, Australia Therapeutic Goods Amendment (Medical Devices) Act 2002, and Therapeutic Goods Amendment (Medical Devices and Other Measures) Act 2009.