ISO 13485 is the medical device industry’s most widely used International Standard for quality management. ISO 13485 standard is an effective solution to meet the comprehensive requirements for a QMS in the medical device industry. Adopting ISO 13485 provides a practical foundation for manufacturers to address the EU Medical Device Directive (MDD), and the EU Medical Device Regulation (MDR).
ISO 13485 Certification in Canada is one of the dozens of certifications issued by TopCertifier, the global ISO Certification consulting firm. Canada is a potentially emerging medical sector. ISO 13485 could be used by businesses in the medical device industry to improve standards and increase efficiency. We deliver ISO 13485 certification services to all major locations in Canada, including Toronto,Ottawa,Montreal,Vancouver etc.
By getting ISO 13485 Certified in Canada, there is an opportunity for increased business opportunities in both existing and emerging markets. There is also a general improvement in the quality of the service/product provided to the consumer. Certification gives a distinct edge over your rivals and will help in acquiring new clients.