The Code of Federal Regulations of the United States of AmericaThe Code of Federal Regulations is the codification of the general and permanent rules published in the Federal Register by the executive departments and agencies of the Federal Government. |
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1.5. rezultāts no 5.
548. lappuse
fore expiration of the body ' s term of approval shall submit a letter of such intent
to FDA , at the address in 8900 . 3 ( b ) ( 1 ) , at least 9 months before
relinquishing such authority . ( f ) Transfer of records . An accreditation body that
does not ...
fore expiration of the body ' s term of approval shall submit a letter of such intent
to FDA , at the address in 8900 . 3 ( b ) ( 1 ) , at least 9 months before
relinquishing such authority . ( f ) Transfer of records . An accreditation body that
does not ...
551. lappuse
( ii ) All clinical images submitted by facility to the accreditation body hall be
reviewed independently by two ir more review physicians . ( 4 ) Selection of
clinical images for reriew . Unless otherwise specified by DA , the accreditation
body shall ...
( ii ) All clinical images submitted by facility to the accreditation body hall be
reviewed independently by two ir more review physicians . ( 4 ) Selection of
clinical images for reriew . Unless otherwise specified by DA , the accreditation
body shall ...
552. lappuse
Accreditation bodies shall ensure that all of their phantom image reviewers : ( i )
Meet the requirements specified in $ 900 . 12 ( a ) ( 3 ) or alternative require -
ments established by the accreditation body and approved by FDA in accordance
...
Accreditation bodies shall ensure that all of their phantom image reviewers : ( i )
Meet the requirements specified in $ 900 . 12 ( a ) ( 3 ) or alternative require -
ments established by the accreditation body and approved by FDA in accordance
...
554. lappuse
1999 ) ( 1 ) Provide a mechanism for all fa - ( 2 ) At FDA ' s request , accreditation
cilities it accredits to file serious unre - bodies shall provide financial records
solved complaints with the accredita - or other material to assist FDA in astion
body ...
1999 ) ( 1 ) Provide a mechanism for all fa - ( 2 ) At FDA ' s request , accreditation
cilities it accredits to file serious unre - bodies shall provide financial records
solved complaints with the accredita - or other material to assist FDA in astion
body ...
555. lappuse
ance , FDA may reinstate approval of the accreditation body . ( 3 ) FDA may
request additional information or establish additional conditions that must be met
by a former accreditation body before FDA approves the reapplication . ( 4 ) FDA
may ...
ance , FDA may reinstate approval of the accreditation body . ( 3 ) FDA may
request additional information or establish additional conditions that must be met
by a former accreditation body before FDA approves the reapplication . ( 4 ) FDA
may ...
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Populāri fragmenti
11. lappuse - Insufficiency of label space for the prominent placing of such word, statement, or information, resulting from the use of label space for any word, statement, design, or device which is not required by or under authority of the act to appear on the label; (5) Insufficiency of label space for the...
18. lappuse - Act (1) small open containers of fresh fruits and fresh vegetables and (2) food which is, in accordance with the practice of the trade, to be processed, labeled, or repacked in substantial quantities at establishments other than those where originally processed or packed, on condition that such food is not adulterated or misbranded under the provisions of this Act upon removal from such processing, labeling, or repacking establishment.
356. lappuse - Act. (b) References in this part to regulatory sections of the Code of Federal Regulations are to Chapter I of Title 21, unless otherwise noted.
86. lappuse - In computing any period of time prescribed or allowed by this part, the day of the act, event, or default after which the designated period of time begins to run is not to be included. The last day of the period so computed is to be included, unless it is...
79. lappuse - label" means a display of written, printed, or graphic matter upon the immediate container of any substance; and a requirement made by or under authority of this Act that any word, statement, or other information appear on the label shall not be considered to be complied with unless such word, statement, or other information also appears...
578. lappuse - Nothing in this section shall authorize the withholding of information by the Secretary or any officer or employee under his control, from the duly authorized committees of the Congress.
15. lappuse - On packages containing 4 pounds or 1 gallon or more and labeled in terms of weight or fluid measure, the declaration shall be expressed in pounds for weight units with any remainder in terms of ounces or common or decimal fractions of the pound; in the case of fluid measure, it shall be expressed in the largest whole unit...
15. lappuse - 6 oz net wt.," and "6 fl oz" or "net contents 6 fl oz". (j) On packages containing 4 pounds or 1 gallon or more and labeled in terms of weight or fluid measure, the declaration shall be expressed in pounds for weight units with any remainder in terms of ounces or common or decimal fractions of the pound...
56. lappuse - (1) the term 'manufacture, preparation, propagation, compounding, or processing' shall include repackaging or otherwise changing the container, wrapper, or labeling of any drug package in furtherance of the distribution of the drug from the original place of manufacture to the person who makes final delivery or sale to the ultimate consumer; "(2) the term 'name...
Bibliogrāfiskā informācija
| Nosaukums | The Code of Federal Regulations of the United States of America |
| Atbalstītāji | United States. Division of the Federal Register, United States. Federal Register Division, United States. Office of the Federal Register |
| Izdevējs | U.S. Government Printing Office, 2006 |
| ISBN | 0160758246, 9780160758249 |
| Eksportēt avotu | BiBTeX EndNote RefMan |