This act seeks to ensure equitable access to life-saving medications by regulating pharmaceutical pricing practices, promoting transparency, and supporting alternative models for drug development and distribution.
Description:
Price Transparency Regulations:
Mandate full public disclosure of the cost structure behind pharmaceutical pricing, including R&D, marketing, production, and profit margins. This data must be audited and published annually by an independent authority.
International Price Benchmarking:
Introduce caps on drug prices based on average international prices in comparable economies. Countries may use a reference pricing model to prevent excessive price disparities.
Compulsory Licensing for Public Health:
Allow governments to issue compulsory licenses for essential medications in the event of price gouging or supply shortages, enabling local or third-party production of generics.
Support for Public and Non-Profit Drug R&D:
Establish a public fund to support research and development of new medications by public institutions and non-profit organizations. Results must remain in the public domain.
Bulk Procurement and Generic Substitution:
Promote joint drug procurement strategies and encourage the use of safe, high-quality generics within national health systems. Provide incentives for pharmacies and hospitals that prioritize cost-effective alternatives.
Ban on Direct-to-Consumer Pharmaceutical Advertising:
Restrict direct marketing of prescription drugs to consumers to reduce demand manipulation and prevent over-prescription driven by commercial interests.
Independent Price Review Board:
Create a national or regional board empowered to investigate and rule on excessive pharmaceutical pricing. It can impose price reductions or penalties when necessary.
Public Education Campaigns:
Launch awareness campaigns to inform the public about generic alternatives, patient rights, and the societal impact of inflated drug pricing.
Possible Outcomes and Implications:
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