The InterMed Group, an exclusive provider of scalable healthcare technology management services, announced the recent certification to ISO 13485:2016, via a news release.
The certification is “a testimony that InterMed’s quality management system meets the most current standards for the service and sale of medical devices as set forth by the International Organization for Standardization [ISO],” according to the release
ISO 13485 is a rigorous standard now considered to be the inline requirement for medical device manufacturers and service providers. For an organization of the InterMed Group’s size, to comply necessitates an on-going team effort and tremendous commitment at all levels of the organization.
“Risk management is heavily emphasized in ISO 13485, demanding detailed and effective communications with our colleagues and customers. This aligns with InterMed’s core values and enhances customer and patient relationships. The industry will benefit as more organizations align their quality management systems to ISO 13485,” Dave Morgan, quality manager for the InterMed Group says.
“Customers can be confident that InterMed takes a risk-based approach with patient safety as a priority, including assurance that we contribute great value toward their legal and regulatory compliance efforts,” Morgan adds.
