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4.
Fed Regist ; 76(71): 20518-24, 2011 Apr 13.
Article in English | MEDLINE | ID: mdl-21491808

ABSTRACT

On October 12, 2010, the President signed the Combat Methamphetamine Enhancement Act of 2010 (MEA). It establishes new requirements for mail-order distributors of scheduled listed chemical products. Mail-order distributors must now self-certify to DEA in order to sell scheduled listed chemical products at retail. Sales at retail are those sales intended for personal use; mail-order distributors that sell scheduled listed chemical products not intended for personal use, e.g., sale to a university, are not affected by the new law. This self-certification must include a statement that the mail-order distributor understands each of the requirements that apply under part 1314 and agrees to comply with these requirements. Additionally, mail-order distributors are now required to train their employees prior to self certification. DEA is promulgating this rule to incorporate the statutory provisions and make its regulations consistent with the new requirements and other existing regulations related to self-certification.


Subject(s)
Certification/legislation & jurisprudence , Commerce/legislation & jurisprudence , Drug and Narcotic Control/legislation & jurisprudence , Drug Packaging/legislation & jurisprudence , Ephedrine , Humans , Inservice Training/legislation & jurisprudence , Methamphetamine , Phenylpropanolamine , Postal Service/legislation & jurisprudence , Pseudoephedrine , United States
5.
Med Klin (Munich) ; 104(2): 163-9, 2009 Feb 15.
Article in German | MEDLINE | ID: mdl-19242667

ABSTRACT

Counterfeit drugs are mainly distributed via the internet. On statement of the World Health Organization (WHO), one medicine out of ten ordered on the internet is counterfeit. Fighting against counterfeits needs close and international cooperation among manufacturers, wholesalers, pharmacies and agencies.


Subject(s)
Drug and Narcotic Control/legislation & jurisprudence , Fraud/legislation & jurisprudence , Illicit Drugs/legislation & jurisprudence , Internet/legislation & jurisprudence , Pharmaceutical Services/legislation & jurisprudence , Postal Service/legislation & jurisprudence , Prescription Drugs , Drug Contamination/legislation & jurisprudence , Drug-Related Side Effects and Adverse Reactions , Fraud/ethics , Germany , Humans , International Cooperation , Internet/ethics , Pharmaceutical Services/ethics , Postal Service/ethics , World Health Organization
13.
Fed Regist ; 68(194): 57799-804, 2003 Oct 07.
Article in English | MEDLINE | ID: mdl-14535265

ABSTRACT

This regulation implements the new threshold requirements and mail order reporting requirements of the Methamphetamine Anti-Proliferation Act of 2000 (MAPA), which was enacted on October 17, 2000. DEA is amending its regulations to reduce the thresholds for pseudoephedrine and phenylpropanolamine for retail distributors and for distributors required to submit mail order reports. Also, DEA is amending its regulations to require mail order reports for certain export transactions. DEA is codifying exemptions from the mail order reporting requirements for certain distributions to nonregulated persons and certain export transactions. This rule is consistent with the intent of MAPA to prevent the diversion of drug products to the clandestine manufacture of methamphetamine and amphetamine, and simultaneously reduce the industry reporting burden.


Subject(s)
Drug Industry/legislation & jurisprudence , Drug and Narcotic Control/legislation & jurisprudence , Legislation, Drug , Methamphetamine/standards , Postal Service/legislation & jurisprudence , Ephedrine/standards , Health Care Sector , Humans , Phenylpropanolamine/standards , United States , United States Food and Drug Administration
17.
Food Drug Law J ; 54(4): 587-98, 1999.
Article in English | MEDLINE | ID: mdl-11824455

ABSTRACT

This article examines ways in which marketers of dietary supplements can make use of the "third-party literature" section of the Dietary Supplement Health and Education Act of 1994 (DSHEA). This provision permits persons or entities, other than manufacturers or distributors, to distribute to consumers certain publications in connection with the sale of particular supplements. These publications may include statements about the therapeutic benefits of such products without subjecting the products to regulation by the Food and Drug Administration (FDA) as unapproved new drugs. Specifically, this article addresses the following: Can a dietary supplement manufacturer or distributor send third-party literature about a dietary supplement to a customer in a mail order sales transaction? Can third-party literature be disseminated by mail with dietary supplement catalogues only? Can third-party literature be disseminated by sales representatives engaged in direct marketing of dietary supplements? Can third-party literature appear on the Internet? The answer appears to be affirmative in each of these situations.


Subject(s)
Dietary Supplements , Internet , Marketing of Health Services , Postal Service/legislation & jurisprudence , Product Labeling/legislation & jurisprudence , Health Promotion , Humans , Literature , United States
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