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<strong>ISTH</strong> <strong>2009</strong> Rules and Regulations<br />

<strong>ISTH</strong> Abstract Embargo Policy<br />

Accepted abstracts are published on a CD-ROM at the Congress (the<br />

“Abstract CD-ROM”). Information contained in abstracts may not be<br />

released until midnight (Eastern Standard Time, North America) July 12,<br />

the opening day of the Congress.<br />

Academic institutions, private organizations and companies with<br />

products whose value may be influenced by information contained in an<br />

abstract, may issue a press release to coincide with the availability of an<br />

abstract on the CD-ROM. However, <strong>ISTH</strong> requires that information going<br />

beyond that contained in the abstract, such as discussion of the abstract,<br />

presentation of data or other details that will be presented at the<br />

Congress, is under embargo as outlined above. Violation of the<br />

embargo may result in the abstract being withdrawn from the Congress<br />

and/or other measures deemed appropriate.<br />

It is not considered a violation of this policy if the information contained<br />

in the abstract is presented or has been accepted for presentation at<br />

another meeting (as noted during abstract submission), or if the abstract<br />

is published in a peer reviewed journal after the abstract submission<br />

deadline.<br />

It is the responsibility of the submitting author to inform interested parties<br />

about this policy.<br />

Food and Drug Administration (FDA)<br />

Approval and Off-Label Indications<br />

The mention (directly or indirectly) of pharmaceutical products not<br />

approved by the FDA for use within the United States is strictly<br />

prohibited. Symposia, conferences, handouts or literature of any kind<br />

that mention such products directly or indirectly are, likewise, prohibited<br />

from display in the exhibit space or in spaces contracted by the <strong>ISTH</strong>.<br />

An exhibiting organization may disseminate from its exhibit space peerreviewed<br />

journal articles about off-label indications of its product(s),<br />

provided the company commits itself to file a supplemental application<br />

based on appropriate research, to establish the safety and effectiveness<br />

of the unapproved use.<br />

16<br />

XXII ND CONGRESS OF THE INTERNATIONAL SOCIETY ON THRO<strong>MB</strong>OSIS AND HAEMOSTASIS

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