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" 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. "
The Code of Federal Regulations of the United States of America - 356. lappuse
2006
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The Code of Federal Regulations of the United States of America

1996
...equivalent to other devices, as required by §807.87. (c) To avoid duplicative listings, an orthopedic device that has two or more types of uses (eg, used both as a diagnostic device and as a surgical device) is listed in one subpart only. (d) References in this part to regulatory sections...
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The Code of Federal Regulations of the United States of America

2002
...each condition in this part and each general condition established in §330.1 of this chapter. (b) References in this part to regulatory sections of...Code of Federal Regulations are to chapter I of title 212 unless otherwise noted. ! 346.3 Definitions. As used in this part: (a) Analgesic, anesthetic drug....
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The Code of Federal Regulations of the United States of America

1993
...duplicative listings. > cardiovascular device that has two or more types of uses (eg, used both ass diagnostic device and as a therapeutic device) is...only in one subpart. (d) References in this part to regula tory sections of the Code of FederaRegulations are to Chapter I of Title 21, unless otherwise...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1996
...subpart and each of the general conditions established in II (b) References in this subpart to regatory sections of the Code of Federal Regulations are to chapter I of title 21 unless otherwise noted. {333.103 Definitions. As used in this subpart: (a) Antibiotic drug. In accordance with section 507(a)...
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The Code of Federal Regulations of the United States of America

1994
...subpart and each general condition established in {330.1 of this chapter. (b) References in this subpart to regulatory sections of the Code of Federal Regulations are to chapter I of title 21 anlese otherwise noted. 43ШОЗ Definitions. As used in this subpart: (a) Acne. A disease involving...
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The Code of Federal Regulations of the United States of America

1996
...subpart and each general condition established in §330.1 of this chapter. (b) Reference In this subpart to regulatory sections of the Code of Federal Regulations are to chapter I of title 21 uniese otherwise noted. {333.203 Definitions. As used in this subpart: (a) Antifungal. A drug which...
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The Code of Federal Regulations of the United States of America

1988
...devices, as required by § 807.87. (c) To avoid duplicative listings, a general hospital and personal use device that has two or more types of uses (eg, used both as a diagnostic § 880.2400 device and as a therapeutic device) is listed only in one subpart. (d) References in this...
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The Code of Federal Regulations of the United States of America

1999
...equivalent to other devices, as required by §807.87. (c) To avoid duplicative listings, a cardiovascular device that has two or more types of uses (eg, used both as a 21 CFR Ch. I (4-1-99 Edition) diagnostic device and as a therapeutic device) is listed only in one...
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Agriculture, Rural Development, and Related Agencies ..., 4. sējums,1. daļa

United States. Congress. House. Committee on Appropriations. Subcommittee on Agriculture, Rural Development, and Related Agencies - 1981
...comply. is subject to regulatory action. (b) References in this part to regulatory sections of tha Code of Federal Regulations are to Chapter I of Title 21. unless otherwise noted. •rsJ Register / Vol. 45. No. 179 / Friday. September 12. I960 / Rulea and Regulation* j definitions...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1985
...addition to each of the general conditions established in § 330.1. (b) References in this subpart to regulatory sections of the Code of Federal Regulations...are to Chapter I of Title 21 unless otherwise noted. § 357.203 Definition. As used in this subpart: Cholecystokinetic drug product A drug product that...
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