What is Drug Labeling?
Drug labeling refers to all the printed material that accompanies a drug, including the label, the wrapping, and the package insert.
Drug labeling refers to all the printed material that accompanies a drug, including the label, the wrapping, and the package insert.
Yes, an IND application is a request to the FDA for authorization to administer an investigational drug (or biologic) to human or a marketed drug in a new indication and/or patient population. However, there are IND Exemptions. Please refer to the section on IND Exemptions for more information.
An investigational drug is defined as:
The term includes drugs (including botanicals, biologicals, and gene therapy, and genetically derived products that meet the definition of a “drug”), and medical devices for human use. The FDA has statutory authority to regulate the development and marketing of these products.
Export Control applies for all export control licenses on behalf of the University. NOTE: Obtaining an export license may take several months and there is no guarantee that the U.S. government will approve a license request.
Primary Investigators (PIs) are responsible for:
Research is not subject to export controls if it qualifies for at least one of three exclusions:
(1) Fundamental research exclusion;
(2) Public domain exclusion; and
(3) Education Information Exclusion.
The Fundamental research exclusion is a broad-based general legal exclusion to protect technical information (but not tangible items) involved in research from being controlled by export controls. In other words, research qualifying as “fundamental research” is not subject to export controls.
The public domain exclusion applies to information that is published and that is generally accessible or available to the public through: