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Complete Book PDF (4.12MB) - World Bank eLibrary

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42 Diagnosing Corruption in Ethiopia<br />

• Consolidating procurement in a specialized agency such as the PFSA<br />

has the potential to substantially improve the quality of procurement.<br />

However, the benefits of consolidation also come with the risk of concentrating<br />

opportunities for abuse. Therefore, the government would<br />

be well advised to establish strong independent oversight for the<br />

PFSA.<br />

Pharmaceuticals<br />

Within health systems, the production, sale, and distribution of pharmaceuticals<br />

are recognized as particularly vulnerable to corruption.<br />

Pharmaceuticals are highly regulated, markets are restricted, and manufacturers<br />

are often politically and economically powerful. It can be costly<br />

for regulators and purchasers to assess the quality and efficacy of pharmaceuticals.<br />

For all these reasons, as figures 2.2 and 2.3 previously enumerated,<br />

abuse and fraud are possible in almost every transaction involving<br />

pharmaceuticals—influencing policies, manipulating decisions about<br />

which drugs to include in national drug lists, corrupting prescription practices,<br />

overprescribing, encouraging kickbacks in procurement, and supplying<br />

substandard products. Corruption in drug system management can<br />

happen at any stage in the process, from basic research to prescription and<br />

use (WHO 2006). The following processes are especially vulnerable:<br />

• Drug selection for the national formulary. As in most countries, Ethiopia<br />

has a list of registered medicines that can be legally imported, produced,<br />

and distributed. The process for including medicines in such a list can be<br />

corrupted by manufacturers who either want to sell products that do<br />

not meet accepted standards or want to exclude competitors. The most<br />

common way to insulate drug registration from abuse is to establish a<br />

procedure for disinterested individuals to serve on a public committee<br />

that applies explicit criteria according to established procedures.<br />

• Medicine promotion. Pharmaceutical manufacturers and distributors<br />

can manipulate the public through advertising or improperly influence<br />

health professionals to increase profits at the expense of patients or<br />

patient health. Few developing countries have effective policies to regulate<br />

medicine promotion.<br />

• Pharmaceutical inspection. Manufacturers, distributors, and retailers can<br />

evade regulations by corrupting inspectors, with detrimental impact on<br />

health and safety.<br />

• Drug distribution. A variety of corrupt practices can also occur at all<br />

points where drugs are distributed, prescribed, purchased, or sold to<br />

patients.

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