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For Medical Device & Quality Management Systems, InterMed Demonstrates Commitment to Compliance & Industry Regulations
Alachua, FL: Today, the InterMed Group, an exclusive provider of scalable healthcare technology management services, announced the recent certification to ISO 13485:2016, 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.] 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.

About the InterMed Group
The InterMed Group is a healthcare technology management services provider, powered by innovation and expansive industry experience. Our unique approach to management has positioned us leaders in healthcare technology management, including cybersecurity profiling, biomedical, clinical, and diagnostic imaging equipment procurement, restoration, and lifecycle management to healthcare facilities and clinics across the United States for almost 30 years.