Name: Regulatory Processes for Rare Disease Drugs in the United States and European Union - National Academies of Sciences, Engineering, 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
Price: 64.6 EUR
Author: National Academies of Sciences, Engineering, 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
ISBN: 9780309726559

Regulatory Processes for Rare Disease Drugs in the United States and European Union

Flexibilities and Collaborative Opportunities

National Academies of Sciences, Engineering, 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 - Regulatory Processes for Rare Disease Drugs in the United States and European Union

Omschrijving

Rare diseases, such as sickle cell disease and thalassemia, affect up to 30 million people in the United States and at least 300 million across the globe.

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Schrijver: National Academies of Sciences, Engineering, 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
Titel: Regulatory Processes for Rare Disease Drugs in the United States and European Union
Uitgever: National Academies Press

Jaar: 2024
Taal: Engels
Pagina's: 386

EAN: 9780309726559
Bindwijze: Paperback

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Regulatory Processes for Rare Disease Drugs in the United States and European Union

Flexibilities and Collaborative Opportunities

Omschrijving

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