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ビジネス · 2018/10/161 分で読めます

Rare Diseases: Early Drug Development and the Role of Pre-Investigational New Drug Application Meetings; Draft Guidance for Industry; Availability

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概要

The Food and Drug Administration (FDA or Agency) is announcing the availability of a draft guidance for industry entitled "Rare Diseases: Early Drug Development and the Role of Pre-Investigational New Drug Application Meetings." The purpose of this draft guidance is to assist sponsors of drug and biological products for the treatment of rare diseases in planning and conducting more efficient and productive pre-investigational new drug application (pre-IND) meetings. Drug development for rare diseases has many challenges related to the nature of these diseases. This draft guidance is intended to advance and facilitate the development of drugs and biological products for the treatment of rare diseases.

情報源の原言語: Federal Register — Food and Drug Administration原文の発表を開く →

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