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International Cooperation on Harmonisation of Technical Requirements for Approval of Veterinary Medicinal Products (VICH); final guidance for industry on "studies to evaluate the safety of residues of veterinary drugs in human food: genotoxicity testing" (VICH GL23); availability. Notice.

• Authors : Food and Drug Administration, HHS

Subjects: Food Contamination* ; Guidelines as Topic* ; International Cooperation*

• Source: Federal register [Fed Regist] 2002 Jan 04; Vol. 67 (3), pp. 602-3.Publisher: Office of the Federal Register, National Archives and Records Service, General Services Administration; distribution by the Supt. of Docs., U. S.

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International Cooperation on Harmonisation of Technical requirements for Approval of Veterinary Medicinal Products (VICH); final guidance on " Safety studies for veterinary drug residues in human food: reproduction toxicity testing" (VICH GL22); availability. Notice.

• Authors : Food and Drug Administration, HHS

Subjects: Food Contamination* ; Guidelines as Topic* ; International Cooperation*

• Source: Federal register [Fed Regist] 2002 Jan 04; Vol. 67 (3), pp. 603-5.Publisher: Office of the Federal Register, National Archives and Records Service, General Services Administration; distribution by the Supt. of Docs., U. S.

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International Conference on Harmonisation; guidance on Q1A stability testing of new drug substances and products; availability. Notice.

• Authors : Food and Drug Administration, HHS

Subjects: Drug Stability* ; Guidelines as Topic* ; International Cooperation*

• Source: Federal register [Fed Regist] 2001 Nov 07; Vol. 66 (216), pp. 56332-3.Publisher: Office of the Federal Register, National Archives and Records Service, General Services Administration; distribution by the Supt. of Docs., U. S.

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International Conference on Harmonisation; guidance on M4 common technical document; availability. Notice.

• Authors : Food and Drug Administration, HHS

Subjects: Guidelines as Topic* ; International Cooperation* ; Legislation, Drug*

• Source: Federal register [Fed Regist] 2001 Oct 16; Vol. 66 (200), pp. 52634-7.Publisher: Office of the Federal Register, National Archives and Records Service, General Services Administration; distribution by the Supt. of Docs., U. S.

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International Conference on Harmonisation; guidance on good manufacturing practice for active pharmaceutical ingredients; availability. Notice.

• Authors : Food and Drug Administration, HHS

Subjects: Guidelines as Topic* ; International Cooperation* ; United States Food and Drug Administration*

• Source: Federal register [Fed Regist] 2001 Sep 25; Vol. 66 (186), pp. 49028-9.Publisher: Office of the Federal Register, National Archives and Records Service, General Services Administration; distribution by the Supt. of Docs., U. S.

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International Conference on Harmonisation; guidance on S7A safety pharmacology studies for human pharmaceuticals; availability. Notice.

• Authors : Food and Drug Administration, HHS

Subjects: Guidelines as Topic* ; International Cooperation* ; United States Food and Drug Administration*

• Source: Federal register [Fed Regist] 2001 Jul 13; Vol. 66 (135), pp. 36791-2.Publisher: Office of the Federal Register, National Archives and Records Service, General Services Administration; distribution by the Supt. of Docs., U. S.

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International Conference on Harmonisation; guidance on E11 clinical investigation of medicinal products in the pediatric population; availability. Notice.

• Authors : Food and Drug Administration, HHS

Subjects: Guidelines as Topic* ; International Cooperation* ; United States Food and Drug Administration*

• Source: Federal register [Fed Regist] 2000 Dec 15; Vol. 65 (242), pp. 78493-4.Publisher: Office of the Federal Register, National Archives and Records Service, General Services Administration; distribution by the Supt. of Docs., U. S.

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International Conference on Harmonisation; guidance on specifications: test procedures and acceptance criteria for biotechnological/biological products. Notice. Food and Drug Administration, HHS.

Subjects: Guidelines as Topic* ; International Cooperation* ; United States Food and Drug Administration*

• Source: Federal register [Fed Regist] 1999 Aug 18; Vol. 64 (159), pp. 44928-35.Publisher: Office of the Federal Register, National Archives and Records Service, General Services Administration; distribution by the Supt. of Docs., U. S.

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International Conference on Harmonisation; guidance on the duration of chronic toxicity testing in animals (rodent and nonrodent toxicity testing); availability. Notice. Food and Drug Administration, HHS.

Subjects: Guidelines as Topic* ; International Cooperation* ; United States Food and Drug Administration*

• Source: Federal register [Fed Regist] 1999 Jun 25; Vol. 64 (122), pp. 34259-60.Publisher: Office of the Federal Register, National Archives and Records Service, General Services Administration; distribution by the Supt. of Docs., U. S.

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International Conference on Harmonisation; guidance on quality of biotechnological/biological products: derivation and characterization of cell substrates used for production of biotechnological/biological products; availability. Notice. Food and Drug Administration, HHS.

Subjects: International Cooperation* ; Quality Assurance, Health Care* ; United States Food and Drug Administration*

• Source: Federal register [Fed Regist] 1998 Sep 21; Vol. 63 (182), pp. 50244-9.Publisher: Office of the Federal Register, National Archives and Records Service, General Services Administration; distribution by the Supt. of Docs., U. S.

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