Search results for: United States. Food and Drug Administration
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281
Guidance for the public, FDA advisory committee members, and FDA staff on procedures for determining conflict of interest and eligibility for participation in FDA advisory committe...
Published: U.S. Dept. of Health and Human Services, Food and Drug Administration, 2008Physical Description: 25 pages : digital, PDF fileConnect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
282
Information sheet guidance for sponsors, clinical investigators, and IRBs : frequently asked questions, statement of investigator (form FDA 1572).
Published: U.S. Dept. of Health and Human Services, Food and Drug Administration, 2008Physical Description: 11 pages : digital, PDF fileConnect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
283
Food allergies : reducing the risks.
Published: U.S. Food and Drug Administration, 2009Physical Description: 2 pages : digital, PDF fileConnect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
284
Food allergies : rare but risky.
Published: U.S. Food and Drug Administration, 2004Physical Description: 1 electronic text : HTML fileConnect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
285
Counterfeit drugs questions and answers.
Published: U.S. Food and Drug Administration, 2003Physical Description: 1 electronic text : HTML fileConnect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
286
Guidance for clinical investigators, institutional review boards, and sponsors : process for handling referrals to FDA under 21 CFR 50.54 : additional safeguards for children in cl...
Published: U.S. Dept. of Health and Human Services, Food and Drug Administration, 2006Physical Description: i, 9 pages : digital, PDF fileConnect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
287
Guidance for industry : advisory committee meetings : preparation and public availability of information given to advisory committee members.
Published: U.S. Dept. of Health and Human Services, Food and Drug Administration, 2008Physical Description: 20 pages : digital, PDF fileConnect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
288
Guidance for FDA advisory committee members and FDA staff : voting procedures for advisory committee meetings.
Published: U.S. Dept. of Health and Human Services, Food and Drug Administration, 2008Physical Description: 6 pages : digital, PDF fileConnect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
289
Guidance for the public, FDA advisory committee members, and FDA staff : public availability of advisory committee members' financial interest information and waivers.
Published: U.S. Dept. of Health and Human Services, Food and Drug Administration, 2008Physical Description: 14 pages : digital, PDF fileConnect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
290
Guidance for the public and FDA staff on convening advisory committee meetings.
Published: U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Biologics Evaluation and Research, 2008Physical Description: 6 pages : digital, PDF fileConnect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
291
Data elements and standards for drug dictionaries, M5.
Published: [U.S. Dept. of Health and Human Services, Food and Drug Administration], 2005Physical Description: 31 pages : digital, PDF fileConnect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
292
Information sheet : guidance for institutional review boards and clinical investigators (frequently asked questions).
Published: [U.S. Dept. of Health and Human Services, Food and Drug Administration], 1998Physical Description: 1 electronic text : HTML fileConnect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
293
Information sheet : guidance for institutional review boards and clinical investigators (cooperative research).
Published: [U.S. Dept. of Health and Human Services, Food and Drug Administration], 1998Physical Description: 1 electronic text : HTML fileConnect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
294
Information sheet : guidance for institutional review boards and clinical investigators (sponsor - investigator - IRB interrelationship).
Published: [U.S. Dept. of Health and Human Services, Food and Drug Administration], 1998Physical Description: 1 electronic text : HTML fileConnect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
295
Information sheet : guidance for institutional review boards and clinical investigators (acceptance of foreign clinical studies).
Published: [U.S. Dept. of Health and Human Services, Food and Drug Administration], 1998Physical Description: 1 electronic text : HTML fileConnect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
296
Information sheet : guidance for institutional review boards and clinical investigators (continuing review after study approval).
Published: [U.S. Dept. of Health and Human Services, Food and Drug Administration], 1998Physical Description: 1 electronic text : HTML fileConnect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
297
Information sheet : guidance for institutional review boards and clinical investigators (charging for investigational products).
Published: [U.S. Dept. of Health and Human Services, Food and Drug Administration], 1998Physical Description: 1 electronic text : HTML fileConnect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
298
Information sheet : guidance for institutional review boards and clinical investigators (recruiting study subjects).
Published: [U.S. Dept. of Health and Human Services, Food and Drug Administration], 1998Physical Description: 1 electronic text : HTML fileConnect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
299
Information sheet : guidance for institutional review boards and clinical investigators (payment to research subjects).
Published: [U.S. Department of Health and Human Services, Food and Drug Administration], 1998Physical Description: 1 electronic text : HTML file.Connect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook -
300
Information sheet : guidance for institutional review boards and clinical investigators (screening tests prior to study enrollment).
Published: [U.S. Dept. of Health and Human Services, Food and Drug Administration], 1998Physical Description: 1 electronic text : HTML fileConnect to online resource - All users (Federal Depository Library Program Persistant URL)
Government Document Electronic eBook