| Themes | National Drug Policy | Rational Drug Use | Essential Drugs | Access to Drugs | Procurement | Pricing | Supply Systems | Regulation | Monitoring and Quality Assurance | Counterfeiting, Diversion, Corruption | Role of the Private Sector | Pharmaceutical Research and Development | Pharmaceutical Manufacturing Private manufacturers, importers, sales agents, wholesalers and pharmacists are a key element of the real world pharmaceutical market in most countries. In many cases they dominate the market from a quantitative perspective. However, drug policy frequently focuses on the public sector only, thereby leaving the private sector and its customers in a regulatory vacuum. Regulation of the private sector should follow two leading principles: - Provide a framework that allows the private sector to grow and be profitable
- Set and implement rules for the private sector that ensure quality of care, safety and a contribution to public health goals
These two principles lead to certain considerations that inform legislation and regulation of the private sector: - Existing and desired structure (industrialized and integrated or de-centralized and fragmented)
- Information requirements (for statistical and policy purposes)
- Human resource requirements, governance and personal accountability
- Technical requirements e.g. storage conditions and participation in quality circles
- Contracting rules with public providers and insurers
- Self-regulation bodies such as associations
- Tax incentives for desired behavior
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