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

>

MEETINGS / EVENTS

RSS

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

ASA PRACTICE MANAGEMENT 2015

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

>

FDA MEDWATCH ALERTS

November 21, 2014

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

Summary:

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

Summary:

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

November 07, 2014

FDA MedWatch - Nellcor Puritan Bennett, 980 Ventilator System: Class I Recall - Software Issue May Stop Ventilator

Summary:

FDA MedWatch Nellcor Puritan Bennett 980 Ventilator System Class I Recall

>

ASA FEATURED PRODUCT

Add this product to your shopping cart

Self-Education and Evaluation (SEE) Program

SKU: 30701-14CE

... Read more »

Single Copies, Member Price: $360

ASA Details How the DEA Can Help Alleviate Drug Shortages in Comment Letter to DOJ

Tuesday, July 12, 2011

In addition to the current multifaceted ASA lobbying campaign to help alleviate drug shortages, ASA signed a regulatory comment letter to the Department of Justice (DOJ) recommending they review Drug Enforcement Administration (DEA) regulations involving quotas of controlled substances. The current quota system has been identified by the ASA co-convened Drug Shortage Summit Legislative and Regulatory Activity Work Group as one cause of drug shortages. The letter was signed by eight organizations and businesses including health care providers, drug manufacturers and distributors. 

The letter states, “We firmly support the department’s plan to evaluate regulations that apply to quotas to registered manufacturers of Schedule I and II controlled substances and certain List I chemicals found in 21 C.F.R. §§ 1303, 1315. We believe the current regulations of controlled substances, and in particular the quota system, have negatively impacted patients across America by contributing to the number and duration of drug shortages.”

The letter was signed by the American Hospital Association (AHA), the American Society of Anesthesiologists (ASA), the American Society of Clinical Oncology (ASCO), the American Society of Health-System Pharmacists (ASHP), the Generic Pharmaceutical Association (GPhA), Hospira, Premier Inc. and Teva Pharmaceutical Industries Ltd.

Click here to read the entire letter. 

 

« Back to Washington Alerts