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Results: 5 books (34 items)

3.
Regulatory Processes for Rare Disease Drugs in the United States and European Union: Flexibilities and Collaborative Opportunities.

Regulatory Processes for Rare Disease Drugs in the United States and European Union: Flexibilities and Collaborative Opportunities.

National Academies of Sciences, Engineering, and Medicine; Health and Medicine Division; Board on Health Sciences Policy; Committee on Processes to Evaluate the Safety and Efficacy of Drugs for Rare Diseases or Conditions in the United States and the European Union; Shore CK, Worku TL, Smith CW, et al., editors.

Washington (DC): National Academies Press (US); 2024 Oct 30.

4.
CADTH Reimbursement Reviews and Recommendations.

CADTH Reimbursement Reviews and Recommendations.

Ottawa (ON): Canadian Agency for Drugs and Technologies in Health; 2013-.

5.
Addressing Sickle Cell Disease: A Strategic Plan and Blueprint for Action.

Addressing Sickle Cell Disease: A Strategic Plan and Blueprint for Action.

National Academies of Sciences, Engineering, and Medicine; Health and Medicine Division; Board on Population Health and Public Health Practice; Committee on Addressing Sickle Cell Disease: A Strategic Plan and Blueprint for Action; Martinez RM, Osei-Anto HA, McCormick M, editors.

Washington (DC): National Academies Press (US); 2020 Sep 10.

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