Use of Advisory Committees by the Food and Drug Administration: Hearings ... Ninety-third Congress Second Session [-Ninety-fourth Congress, First Session] ...U.S. Government Printing Office, 1974 |
From inside the book
Results 1-5 of 86
Page iv
... closed sessions , minutes of the FDA Cardiovascular and Renal Advisory Committee and costs entailed . 311-314 314-317 February 25 , 1974 , open session , eighth meeting of the FDA Ophthalmic Drugs Advisory Committee .. Food and Drug ...
... closed sessions , minutes of the FDA Cardiovascular and Renal Advisory Committee and costs entailed . 311-314 314-317 February 25 , 1974 , open session , eighth meeting of the FDA Ophthalmic Drugs Advisory Committee .. Food and Drug ...
Page v
... closed meeting of Cardi- ovascular - Renal Advisory Committee__ 470 296-310 Working group on use of advisory committees in drug evaluation— avoiding conflict of interests in special Government employees_245-246 Hutt , Peter Barton ...
... closed meeting of Cardi- ovascular - Renal Advisory Committee__ 470 296-310 Working group on use of advisory committees in drug evaluation— avoiding conflict of interests in special Government employees_245-246 Hutt , Peter Barton ...
Page 18
... necessary . At least one hour of open session is provided at the beginning of each meeting to permit comments or presentations by interested persons . The public may participate . E. The closed session ( if any ) is confined 18.
... necessary . At least one hour of open session is provided at the beginning of each meeting to permit comments or presentations by interested persons . The public may participate . E. The closed session ( if any ) is confined 18.
Page 19
... closed session ( if any ) is confined to discussion of matters defined in the Freedom of Information Act . Committee F. members and FDA staff may participate . An executive session usually is defined as a closed session for committee ...
... closed session ( if any ) is confined to discussion of matters defined in the Freedom of Information Act . Committee F. members and FDA staff may participate . An executive session usually is defined as a closed session for committee ...
Page 70
... closed . Nevertheless , at least 1 hour of open session is provided at the begin- ning of each meeting to permit comments or presentations by interested persons . The public may of course participate . Mr. FOUNTAIN . May I interrupt at ...
... closed . Nevertheless , at least 1 hour of open session is provided at the begin- ning of each meeting to permit comments or presentations by interested persons . The public may of course participate . Mr. FOUNTAIN . May I interrupt at ...
Other editions - View all
Common terms and phrases
adequate advice Advisory Committee Act advisory committee meetings agency angina pectoris approval April 13 Apter basis Belton beta blockers BROWN of Ohio Bureau of Drugs carcinogenicity Cardiovascular Chairman clinical trials Commissioner committee members congestive heart failure consultants contraceptive controlled CROUT decision Depo Depo-Provera Devices diethylstilbestrol Director discussion doctors document dosage dose Drug Administration drug application Drug Products estrogens evaluation experts FDA staff FDA's Federal Advisory Committee Federal Register files Food and Drug FOUNTAIN going GOLDBERG GOLDHAMMER HUTT Inderal indication investigator issue judgment labeling marketed matter medical officers Medicine medroxyprogesterone acetate ment minutes mittee opinion package insert Panel on Review patients physician placebo postcoital contraceptive present problem propranolol protocol Provera question recommendations record regulatory Renal Advisory Committee response SCHMIDT scientific specific statement studies subcommittee submitted substantial evidence summary tion treatment verbatim transcript well-controlled
Popular passages
Page 555 - ... (6) personnel and medical files and similar files the disclosure of which would constitute a clearly unwarranted invasion of personal privacy; (7) investigatory files compiled for law enforcement purposes except to the extent available by law to a party other than an agency...
Page 79 - Secretary pursuant to subsection (b), do not include adequate tests by all methods reasonably applicable to show whether or not such drug is safe for use under the conditions prescribed, recommended, or suggested in the proposed labeling...
Page 555 - ... (5) inter-agency or intra-agency memorandums or letters which would not be available by law to a party other than an agency in litigation with the agency; (6) personnel and medical files and similar files the disclosure of which would constitute a clearly unwarranted invasion of personal privacy...
Page 79 - ... substantial evidence" means evidence consisting of adequate and well-controlled investigations, including clinical investigations, by experts qualified by scientific training and experience to evaluate the effectiveness of the drug involved, on the basis of which it could fairly and responsibly be concluded by such experts that the drug will have the effect it purports or is represented to have under the conditions of use prescribed, recommended, or suggested in the labeling or proposed labeling...
Page 549 - advisory committee" means any committee, board, commission, council, conference, panel, task force, or other similar group, or any subcommittee or other subgroup thereof...
Page 474 - Executive order; (2) related solely to the internal personnel rules and practices of an agency; (3) specifically exempted from disclosure by statute; (4) trade secrets and commercial or financial information obtained from a person and privileged or confidential...
Page 6 - FEDERAL ADVISORY COMMITTEE ACT FEDERAL ADVISORY COMMITTEE ACT PUBLIC LAW 92-463 AN ACT To authorize the establishment of a system governing the creation and operation of advisory committees in the executive branch of the Federal Government, and for other purposes.
Page 96 - Detailed minutes of each meeting of each advisory committee shall be kept and shall contain a record of the persons present, a complete and accurate description of matters discussed and conclusions reached, and copies of all reports received, issued, or approved by the advisory committee.
Page 79 - As used in this subsection and subsection (e), the term "substantial evidence" means evidence consisting of adequate and well-controlled investigations, including clinical investigations, by experts qualified by scientific training and experience to evaulate the effectiveness of the drug involved, on the basis of which it could fairly and responsibly be concluded by such experts that the drug will have the effect it purports or is represented to have under the conditions of use prescribed, recommended...
Page 290 - Secretary finds ( 1 ) that the applicant has failed to establish a system for maintaining required records, or has repeatedly or deliberately failed to maintain such records or to make required reports, in accordance with...