Medtech strives to achieve our growth targets all the while respecting responsible ethical rules towards our shareholders, employees, customers and partners.
We are focused on developing higher technological procedures and innovative design by listening to our customer’s needs and by anticipating future requests by providing the most state-of-the-art product possible.
Quality Requirements :
Medtech holds the highest degree of respect and adherence to an overall high-level quality approach. Consequently ROSA® has achieved the necessary and varied certifications which support its conformity with both national and international standards of quality and reliability, namely :
- ISO Standards 13485 and ISO 9001: confirming achievements in required quality management systems for the medical device industry.
- CE mark establishing regulatory requirements achieved, valid within the European Union.
- Health Canada approval which references the country’s requirements governing medical instruments.
- Food and Drug Administration Approval (FDA), allows for the marketing of a medical device in the United States.
Environmental Regulations :
To ensure the most minimal impact to our environment, we strive to optimize our waste management. We maintain that our products respect all the environmental regulations no matter their country of ultimate destination.