[Download] "Final Rule re Investigational New Drug Safety Reporting Requirements for Human Drug and Biological Products - Safety Reporting Requirements (US Food and Drug Administration Regulation) (FDA) (2018 Edition)" by The Law Library " eBook PDF Kindle ePub Free

Final Rule re Investigational New Drug Safety Reporting Requirements for Human Drug and Biological Products - Safety Reporting Requirements (US Food and Drug Administration Regulation) (FDA) (2018 Edition)

eBook details

Title: Final Rule re Investigational New Drug Safety Reporting Requirements for Human Drug and Biological Products - Safety Reporting Requirements (US Food and Drug Administration Regulation) (FDA) (2018 Edition)
Author : The Law Library
Release Date : January 06, 2018
Genre: Law,Books,Professional & Technical,
Pages : * pages
Size : 283 KB

Description

The Law Library presents the complete text of the Final Rule re Investigational New Drug Safety Reporting Requirements for Human Drug and Biological Products - Safety Reporting Requirements (US Food and Drug Administration Regulation) (FDA) (2018 Edition).
Updated as of May 29, 2018

The Food and Drug Administration (FDA) is amending its regulations governing safety reporting requirements for human drug and biological products subject to an investigational new drug application (IND). The final rule codifies the agency's expectations for timely review, evaluation, and submission of relevant and useful safety information and implements internationally harmonized definitions and reporting standards. The revisions will improve the utility of IND safety reports, reduce the number of reports that do not contribute in a meaningful way to the developing safety profile of the drug, expedite FDA's review of critical safety information, better protect human subjects enrolled in clinical trials, subject bioavailability and bioequivalence studies to safety reporting requirements, promote a consistent approach to safety reporting internationally, and enable the agency to better protect and promote public health.

This ebook contains:
- The complete text of the Final Rule re Investigational New Drug Safety Reporting Requirements for Human Drug and Biological Products - Safety Reporting Requirements (US Food and Drug Administration Regulation) (FDA) (2018 Edition)
- A dynamic table of content linking to each section
- A table of contents in introduction presenting a general overview of the structure