Rhode Island 2025 Regular Session

Rhode Island House Bill H5632

Introduced
2/26/25  

Caption

Requires prescription drug manufacturers to file a detailed, updated list of each pharmaceutical sales representative engaged by the manufacturer and to pay an annual fee for each name listed with the department of business regulation.

Impact

If enacted, H5632 would amend Chapter 19 of Title 5 in the General Laws of Rhode Island, thereby instituting a systematic approach to regulating pharmaceutical sales practices. The law aims to contain rising drug costs by documenting and analyzing prescription patterns influenced by sales representatives. Through annual reporting by manufacturers, the Department of Business Regulation would be responsible for compiling a report on the activities of these representatives, which will be accessible to the public as well as relevant health authorities. This could potentially lead to changes in how drugs are marketed and prescribed in the state.

Summary

House Bill H5632, also known as the Prescription Drug Sales Representative Disclosure Act, aims to enhance transparency in the interactions between pharmaceutical manufacturers and healthcare providers in Rhode Island. Under this act, drug manufacturers are mandated to maintain and submit an updated list of their pharmaceutical sales representatives to the Department of Business Regulation. This list must be filed annually and any changes in representation must be reported within 60 days. The act is designed to provide insight into the promotional practices within the pharmaceutical industry, particularly those that influence prescription behaviors of healthcare providers.

Contention

Notably, the bill may face contention regarding the enforcement of penalties for non-compliance, including civil penalties reaching up to $10,000 for manufacturers that fail to provide the required information. Critics could argue that such fines may place additional burdens on pharmaceutical companies and might stifle their ability to operate effectively in the state. The measure also raises questions about the implications of public accessibility to this information on the competitiveness of drug marketing, as it could expose specific strategies of individual manufacturers.

Companion Bills

No companion bills found.

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