Pink Sheet is part of Pharma Intelligence UK Limited

This site is operated by Pharma Intelligence UK Limited, a company registered in England and Wales with company number 13787459 whose registered office is 5 Howick Place, London SW1P 1WG. The Pharma Intelligence group is owned by Caerus Topco S.à r.l. and all copyright resides with the group.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction

NACDS URGES PASSAGE OF DINGELL DRUG DIVERSION BILL

Executive Summary

NACDS URGES PASSAGE OF DINGELL DRUG DIVERSION BILL, expressing "complete support" for the Prescription Drug Marketing Act of 1986. In June 3 letters to House Energy and Commerce Oversight/Investigations Subcmte. Chairman John Dingell (D-Mich.) and Rep. James Broyhill (R-NC), National Assn. of Chain Drug Stores (NACDS) president Robert Bolger stated: "NACDS firmly believes that H.R. 4820 should be scheduled for expeditious consideration. If hearings are necessary, they should be perfunctory coupled with a mark-up session." The NACDS chief exec noted that the bill is based on five days of hearings, 18 months of investigatory work by the subcmte. and documented in detail by an extensive cmte. report. Dingell still is seeking strong evidence for the proposed legislation and has scheduled three drug diversion hearings for July and August. FDA Com. Frank Young is scheduled to testify at the upcoming sessions. Chances for passage of the Prescription Drug Marketing Act are uncertain. Reportedly, House Health Subcmte. Chairman Waxman (D-Calif.) is not planning to schedule hearings and markup on the measure because it is too late in the legislative session. Even if the bill passes the House, support for the measure has not materialized in the Senate. H.R. 4820, which was introduced by Rep. Dingell on May 14, would make distribution of drug samples by pharmaceutical company sales personnel illegal. The bill restricts MD sampling, requiring physicians to request samples in writing from drug firms. The legislation also calls for more strict licensing requirements for whslrs. and prohibits the resale of drugs purchased at nonprofit discounts ("The Pink Sheet" May 26, p. 12). NACDS' endorsement of the drug diversion bill adds to statements of support from other pharmacy groups. American Pharmaceutical Association (APhA) President John Schlegel hailed the legislation as "a major step forward in the Association's 45-year battle to reform drug sampling abuses." In a June release, APhA recommended that Congress revise portions of the bill regarding drug sampling to "more adequately address sampling abuses." The assn. reportedly is working on an amendment that would ban all MD sampling. APhA, however, seems willing to accept the bill as a compromise if passage this year were assured. The American Society of Hospital Pharmacists (ASHP) also supports the drug diversion legislation, though the society is in favor of stronger curbs on sampling. The ASHP June newsletter notes the sampling provisions represent a compromise among subcmte. members who differed considerably on the issue. The newsletter asserts that the bill "is consonant" with ASHP's oral testimony on drug diversion before the House Oversight/Investigations subcmte. last December. The National Assn. of Retail Druggists designates "the enactment of the Prescription Drug Marketing Act as NARD's top priority" in a May 15 letter to members of the House of Representatives. NARD sent the letter the day after Dingell's introduction of H.R. 4820 to ask congressmen to cosponsor the bill. The National Assn. of Boards of Pharmacy (NABP) also expressed its support in a June 2 mailgram to Rep. Dingell following NABP's annual meeting.

You may also be interested in...



Part D Discount Liability Coming Into Focus: CMS Releases Drug Cost Data

Newly released Medicare Part D data sheds light on the sales hit that branded pharmaceutical manufacturers will face when the coverage gap discount program gets under way in 2011

FDA Skin Infections Guidance Spurs Debate On Endpoint Relevance

FDA appears headed for a showdown with clinicians and the pharmaceutical industry over the proposed new clinical trial endpoints for acute bacterial skin and skin structure infections, the guidance's approach for justifying a non-inferiority margin and proposed changes in the types of patients that should be enrolled in trials

Shire Hopes To Sow Future Deals With $50M Venture Fund

Specialty drug maker Shire has quietly begun scouting deals with a brand-new $50 million venture fund, the latest of several in-house investment arms to launch with their parent company's pipelines, not profits, as the measure of their worth

Latest Headlines
See All
UsernamePublicRestriction

Register

PS010305

Ask The Analyst

Ask the Analyst is free for subscribers.  Submit your question and one of our analysts will be in touch.

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel