AN ACT CONCERNING THE CERTIFICATION AND REGULATION OF MEDICAL DEVICE REPRESENTATIVES.

SB 433 requires medical device representatives to obtain certification and adhere to state-set standards. It directly affects professionals who sell or promote medical devices to healthcare facilities. The bill establishes a regulatory framework under Title 21a of the general statutes, mandating certification for these representatives. This creates a formal system to oversee their qualifications and conduct. The stated purpose is to provide structured certification and regulation for this profession.