• Point to reliable information collections and systems, in which different users and user groups (ministries of health, policy makers, health workers, information providers, patients and their families, general public) can focus on the knowledge that best meets their health information needs;

• Act as a facilitator enabling access to information contents produced by numerous key providers – be they commercial companies, government institutions, civil society, not-for-profit organizations, and regional or international bodies;

• Support communities of practice and training

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