July 27, 2016 8:41 PM ET

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Company Overview of United States Department of Health & Human Services

Company Overview

United States Department of Health & Human Services is a government organization that provides health and human services. The organization offers public health, food and drug safety, grants and funding, and health insurance services. Additionally, it provides health and social science research, financial assistance, pre school education, and child abuse and domestic violence prevention services. United States Department of Health & Human Services is based in Washington, District of Columbia.

200 Independence Avenue, S.W.

Washington, DC 20201

United States

Founded in 2007

Phone:

202-619-0257

Key Executives for United States Department of Health & Human Services

Secretary
Age: 50
Secretary
Age: 55
Chief Executive Officer of Beatrice State Developmental Center
Chief of Staff
Deputy Secretary
Compensation as of Fiscal Year 2016.

United States Department of Health & Human Services Key Developments

Food and Drug Administration and Department of Health and Human Services Issue Final Rule About Classification of Nasolacrimal Compression Device into Class I General Controls

Food and Drug Administration and Department of Health and Human Services has issued a final rule called medical devices; Ophthalmic Devices; Classification of Nasolacrimal Compression Device. The Food and Drug Administration is classifying the nasolacrimal compression device into class I. Agency is classifying the device into class I general controls in order to provide a reasonable assurance of safety and effectiveness of the device.

Food and Drug Administration Issues Guidance for Industry on Postmarketing Adverse Event Reporting

Food and Drug Administration, Department of Health and Human Services, has issued a notice called: Agency Information Collection Activities; Announcement of Office of Management and Budget Approval; Guidance for Industry on Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products Marketed Without an Approved Application. The Food and Drug Administration (FDA) is announcing that a collection of information entitled 'Guidance for Industry on Postmarketing Adverse Event Reporting for Nonprescription Human Drug Products Marketed Without an Approved Application' has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995.

Food and Drug Administration and Department of Health and Human Services Issue Final Order on Completion of Product Development Protocol for Surgical Mesh for Transvaginal Pelvic Organ Prolapse Repair

Food and Drug Administration (FDA), Department of Health And Human Services (HHS), has issued a final order called: Effective Date of Requirement for Premarket Approval for Surgical Mesh for Transvaginal Pelvic Organ Prolapse Repair. The final order, published in the Federal Register on Jan. 5 by Leslie Kux, Associate Commissioner for Policy, states: The Food and Drug Administration (FDA or the Agency) is issuing a final order to require the filing of a premarket approval application (PMA) or notice of completion of a product development protocol (PDP) for surgical mesh for transvaginal pelvic organ prolapse (POP) repair.

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