Generics 2030: Where Are We Heading in 2030 for Generic Drug Science, Research, and Regulation?

Author:

Zhang Lei1,Lionberger Robert A.1

Affiliation:

1. Office of Research and Standards Office of Generic Drugs Center for Drug Evaluation and Research US Food and Drug Administration Silver Spring Maryland USA

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

Reference5 articles.

1. Association for Accessible Medicines.2018 generic drug access and savings in the United States (2018). Accessed August 19 2019.

2. US Food and Drug Administration (FDA).GDUFA II performance goals (2016). Accessed August 19 2019.

3. Innovation for Generic Drugs: Science and Research Under the Generic Drug User Fee Amendments of 2012

4. Generating Model Integrated Evidence for Generic Drug Development and Assessment

5. The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) Reflection Paper on “Further Opportunities for Harmonization of Standards for Generic Drugs” (2018). Accessed January 6 2020.

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