Bill > SB00433

This bill proposes to amend Title 21a of the general statutes to establish a certification and regulatory framework for medical device representatives. While the specific details of the proposed regulations are not provided in the text, the bill appears to be aimed at creating a formal process for overseeing professionals who work in the medical device industry, likely to ensure they meet certain professional standards, undergo proper training, and adhere to specific guidelines when representing medical devices to healthcare providers. Medical device representatives typically work for manufacturers and visit hospitals, clinics, and medical practices to provide information about medical equipment, demonstrate product usage, and support healthcare professionals in understanding new medical technologies. By introducing certification requirements, the bill seeks to potentially improve accountability, safety, and professional conduct within this sector.

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https://www.cga.ct.gov/asp/cgabillstatus/cgabillstatus.asp?selBillType=Bill&bill_num=SB00433&which_year=2025