Notice: Get a jump on 2015 — Pay your 2015 ASA membership dues now!




January 23 - 25 2015, 12:00 AM - 12:00 AM


February 07 - 08 2015, 12:00 AM - 12:00 AM

ASA Certificate in Business Administration 2015

June 26 - 28 2015, 12:00 AM - 12:00 AM

Annual Perioperative Surgical Home Summit



December 18, 2014

0.9 Percent Sodium Chloride Injection USP in 100 mL MINI-BAG PLUS Container by Baxter: Recall - Particulate Matter


FDA MedWatch Recall - Particulate Matter

November 21, 2014

FDA MedWatch - Respironics California, Esprit V1000 and V200 Ventilators: Class I Recall - Power Failure May Occur


FDA MedWatch Respironics California Esprit V1000 and V200 Ventilators Class I Recall

November 21, 2014

FDA MedWatch - Highly Concentrated Potassium Chloride Injection, 10 mEq per 100 mL by Baxter: Recall - Mislabeled


Highly Concentrated Potassium Chloride Injection 10 mEq per 100 mL by Baxter Recall Mislabeled



Add this product to your shopping cart

Self-Education and Evaluation (SEE) Program

SKU: 30701-14CE

... Read more »

Single Copies, Member Price: $360

U.S. House of Representatives Passes PDUFA Reauthorization That Includes Drug Shortages Provisions

Thursday, May 31, 2012

On May 30, the U.S. House of Representatives, by a vote of 387-5 passed the Food and Drug Administration Reform Act of 2012, H.R. 5651, commonly referred to as the Prescription Drug User Fee Act (PDUFA) Reauthorization, a legislative package of important Food and Drug Administration (FDA) provisions including one to prevent and mitigate national drug shortages.  Last week, the U.S. Senate passed a separate PDUFA reauthorization bill that also addresses the drug shortage issue.

Title IX of the House PDUFA reauthorization includes specific requirements for enhanced manufacturer notification to FDA that would enable the agency to use its existing authority to respond in a timely fashion to a manufacturer's decision to halt or interrupt production of a key drug.

Other provisions in Title IX of the PDUFA reauthorization would authorize the Secretary of the Department of Health and Human Services (HHS) to process expedited inspections and reviews of drug applications and manufacturing facilities if such actions could help alleviate or mitigate pending drug shortages. ASA was pleased to see that that the Committee included language to "require the Drug Enforcement Administration (DEA) to provide timely approvals or denials of increases in quotas of controlled substances in instances where such an increase could help address a drug shortage." Also, the legislation requires a Government Accountability Office (GAO) Study to examine the issue of drug shortages.

With regard to future consideration of the legislation, the House version of PDUFA must now be reconciled with the Senate version of the measure. A number of differences will need to be addressed by lawmakers. The process of reaching agreement on the differences is expected to begin immediately.

Review the House legislation.
Review the Senate legislation.
Review the Summary of House Passed Legislation.
Learn more about Drug Shortages.
Send the FDA an email reporting a drug shortage.


« Back to Washington Alerts