The Children's Vaccine Initiative Achieving the Vision (1993) / Chapter Skim
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Appendix E: Public Health Service Act (1944)
Appendix E: Public Health Service Act (1944)
Pages 184-188
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From page 184... ...
for sale, barter, or exchange in the District of Columbia, or send, carry, or bring for sale, barter, or exchange from any State or possession into any other State or possession or into any foreign country, or from any foreign country into any State or possession, any virus, therapeutic serum, toxin, antitoxin, or analogous product, or arsphenamine or its derivatives (or any other trivalent organic arsenic compound) , applicable to the prevention, Manufacturers of treatment, or cure of diseases or injuries of man, virus, etc.
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From page 185... ...
each package of such virus, serum, toxin, antitoxin, or other product is plainly marked with the proper name of the article contained therein, the name, address, and license number of the manufacturer, and the date beyond which the specific results. The Effect of suspension or revocation of any license shall not license sus- prevent the sale, barter, or exchange of any virus, pension, etc.
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From page 186... ...
(A) 1 A partially processed biological product which is not in a form applicable to the prevention, treatment, or cure of diseases or injuries of man, which is not intended for sale in the United States, and which is intended for further manufacture into final dosage form outside the United States in a country listed under section Wadded by sec.
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From page 187... ...
The Secretary may not approve an application to export such a product unless the Secretary determines that the product is manufactured, processed, packaged, and held in conformity with current good manufacturing practice and the outside of the shipping package is labeled with the following statement: "This product may be sold or offered for sale only in the following countries: ,~ the blank space being filled with a list of the countries to which export of the drug is authorized.
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From page 188... ...
(b) The Service may prepare any product described in section 351 for the use of other Federal departments or agencies, and public or private agencies and individuals engaged in work in the field of medicine when such product is not available from establishments licensed under such section.
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