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" A statement as to whether the drug is (.or is not) limited in its labeling and by this application to use under the professional supervision of a practitioner licensed by law to administer it. "
Regulation of Diethylstilbestrol (DES), 1975: Joint Hearing Before the ... - Էջ 186
United States. Congress. Senate. Committee on Labor and Public Welfare - 1975 - 304 էջ
Ամբողջությամբ դիտվող - Այս գրքի մասին

Code of Federal Regulations: Containing a Codification of Documents of ...

1977 - 1080 էջ
...of Initial placement of any such advertising for a prescription drug (see 5 310.300 of the nev/-drug regulations). Approval of a supplemental newdrug application...its labeling and by this application to use under the professional supervision of a practitioner licensed by law to administer it. 6. A full list of...
Ամբողջությամբ դիտվող - Այս գրքի մասին

The Code of Federal Regulations of the United States of America

1969 - 668 էջ
...and at the tune of initial placement of any such advertising for a prescription drug (see § 130.13 of the new-drug regulations). Approval of a supplemental...covered by the approved application.) 5. A statement аз to whether the drug is (or is not) limited in its labeling and by this application to use under...
Ամբողջությամբ դիտվող - Այս գրքի մասին

Code of Federal Regulations: Containing a Codification of Documents of ...

1981 - 1252 էջ
...and at the time of initial placement of any such advertising for a prescription drug (see § 310.300 of the new-drug regulations). Approval of a supplemental...promotional claims not covered by the approved application.) g. If the drug is limited in its labeling to use under the professional supervision of a practitioner...
Ամբողջությամբ դիտվող - Այս գրքի մասին

Code of Federal Regulations: Containing a Codification of Documents of ...

1979 - 1056 էջ
...and at the time of initial placement of any such advertising for a prescription drug (see { 310.300 of the new-drug regulations). Approval of a supplemental...promotional claims not covered by the approved application.) g. If the drug is limited in its labeling to use under the professional supervision of a practitioner...
Ամբողջությամբ դիտվող - Այս գրքի մասին

Code of Federal Regulations: Containing a Codification of Documents of ...

1958 - 342 էջ
...application will be submitted as soon as available and prior to the marketing of the drug. (7) State whether the drug is (or is not) limited in its labeling and by this application to use under the professional supervision of a practitioner licensed by law to administer it. (8) If this is a supplemental...
Ամբողջությամբ դիտվող - Այս գրքի մասին

Hearings, Reports and Prints of the Senate Committee on the ..., Հատոր 20-22

United States. Congress. Senate. Committee on the Judiciary - 1960 - 1250 էջ
...application will be submitted as soon as available and prior to the marketing of the drug. (7) State whether the drug Is (or Is not) limited In Its labeling and by this application to use under the professional supervision of a practitioner licensed by law to administer It. (8) If thl* Is a supplemental...
Ամբողջությամբ դիտվող - Այս գրքի մասին

Code of Federal Regulations: Containing a Codification of Documents of ...

1963 - 1386 էջ
...submitts* as soon as available and prior to the marketing of the drug. (7) State whether the drug la (or Is not) limited in its labeling and by this application to use under the professional supervision of a practitioner licensed by law to admlnlsar it. (8) If this is a supplemental...
Ամբողջությամբ դիտվող - Այս գրքի մասին

Code of Federal Regulations: Containing a Codification of Documents of ...

1964 - 1784 էջ
...drug, copies of proposed advertising may be submitted optionally for comment or approval.) 7. State whether the drug is (or Is not) limited In its labeling and by this application to use under the professional supervision of a practitioner licensed by law to administer it. 8. If this Is a supplemental...
Ամբողջությամբ դիտվող - Այս գրքի մասին

Drug Safety: Hearings Before a Subcommittee of the Committee on Government ...

United States. Congress. House. Committee on Government Operations - 1964 - 844 էջ
...drug, copies of proposed advertising may be submitted optionally for comment or approval.) 7. State whether the drug is (or is not) limited in its labeling and by this application to use under the professional supervision of a practitioner licensed by law to administer it. 8. If this is a supplemental...
Ամբողջությամբ դիտվող - Այս գրքի մասին

Competitive Problems in the Drug Industry: Hearings Before Subcommittee on ...

United States. Congress. Senate. Select Committee on Small Business. Subcommittee on Monopoly - 1975 - 888 էջ
...prescription drug (see SHO.IJ of the new-drag regulations). Approvsl of a supplemental new-drug application ia required prior to use of any promotional claims not...application.) 5. A statement as to whether the drug is (ot is pop limited in it* labeling and by this application to use uotfer the professional supervision...
Ամբողջությամբ դիտվող - Այս գրքի մասին




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