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" ... drug, based on a fair evaluation of all material facts, is false or misleading in any particular and was not corrected within a reasonable time after receipt of written notice from the Secretary specifying the matter complained of. Any order under... "
Code of Federal Regulations: Containing a Codification of Documents of ... - 156. lappuse
2001
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United States Code, 6. sējums

United States - 1977 - 1276 lapas
...evaluated together with the evidence before him when the application was approved, the labeling of such drug, based on a fair evaluation of all material facts, is false or misleading in any particular and was not corrected within a reasonable time after receipt of written notice from the Secretary specifying...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1998 - 1120 lapas
...used in, or §314.150 §314.150 the facilities and controls used for, the manufacture, processing1, and packing of the drug are Inadequate to ensure and...based on a fair evaluation of all material facts, la false or misleading in any particular, and the labeling was not corrected by the applicant within...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1986 - 1610 lapas
...on the basis of new information before FDA, evaluated together with the evidence available when the application was approved, the labeling of the drug,...to comply with the notice requirements of section 510CJX2) of the act. (5) That the applicant has failed to submit bioavailability or bioequivalence...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1998 - 1120 lapas
...evaluated together with the evidence available when the application or abbreviated application «u approved, the labeling of the drug, based on a fair...to comply with the notice requirements of section 51<Xj)(2) of the act. (5) That the applicant has failed to «nbmit bloavailability or bioequlvabce...
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The Code of Federal Regulations of the United States of America

2002 - 628 lapas
...evaluated together with the evidence before him when the application was approved, the labeling of such drug, based on a fair evaluation of all material facts, is false or misleading in any particular and was not corrected within a reasonable time after receipt of written notice from the Secretary specifying...
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The Code of Federal Regulations of the United States of America

2001 - 620 lapas
...evaluated together with the evidence before him when the application was approved, the labeling of such drug, based on a fair evaluation of all material facts, is false or misleading in any particular and was not corrected within a reasonable time after receipt of written notice from the Secretary specifying...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1981 - 738 lapas
...the evidence before him when the application was approved, the labeling of such drug or animal feed, based on a fair evaluation of all material facts, is false or misleading in any particular and was not corrected within a reasonable time after receipt of written notice from the Secretary specifying...
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The Code of Federal Regulations of the United States of America

2006 - 616 lapas
...together with the evidence before him when such license was issued, the labeling of any animal feeds, based on a fair evaluation of all material facts, is false or misleading in any particular and was not corrected within a reasonable time after receipt of written notice from the Commissioner specifying...
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The Code of Federal Regulations of the United States of America

1971 - 676 lapas
...application was approved, the labeling of the drug, based Chapter I — Food and Drug Administration on a fair evaluation of all material facts, Is false or misleading in any particular; and that the matter complained of was not corrected by the applicant within a reasonable time after his...
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Drug Safety: Hearings Before a Subcommittee of the Committee on Government ...

United States. Congress. House. Committee on Government Operations - 1964 - 844 lapas
...information before the Food and Drug Administration, evaluated together with the evidence available when the application was approved, the labeling of the drug,...all material facts, is false or misleading in any particluar ; aud that the matter complained of was not corrected by the applicant within a reasonable...
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