Slēptie lauki
Grāmatas Grāmatas
" The investigator is required to furnish his reports to the sponsor of the drug who is responsible for collecting and evaluating the results obtained by various investigators. The sponsor is required to present progress reports to the Food and Drug Administration... "
Code of Federal Regulations: Containing a Codification of Documents of ... - 84. lappuse
2001
Pilnskats - Par šo grāmatu

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

1992 - 1120 lapas
...control number 0910-0014) 152 PR 8831, Mar. 19, 1987, as amended at 82 PR 23031, June 17, 1987] § 312.64 Investigator reports. (a) Progress reports....the results obtained. The sponsor is required under I 312.33 to submit annual reports to PDA on the progress of the clinical investigations. (b) Safety...
Pilnskats - Par šo grāmatu

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

1991 - 1218 lapas
...under control number 0910-0014) [52 PR 8831, Mar. 19. 1987. as amended at 52 PR 23031, June 17, 1987] 8 312.64 Investigator reports. (a) Progress reports....the results obtained. The sponsor is required under 1312.33 to submit annual reports to PDA on the progress of the clinical investigations. (b) Safety...
Pilnskats - Par šo grāmatu

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

1981 - 1252 lapas
...drug or employed as a control in the investigation. d. The investigator is required to furnish his reports to the sponsor of the drug who is responsible...for collecting and evaluating the results obtained by various investigators. The sponsor is required to present progress reports to the Food and Drug...
Pilnskats - Par šo grāmatu

Drug Industry Act of 1962, Hearings ... 87-2 ... June 19, 20, 21, 22, August ...

United States. Congress. House. Interstate and Foreign Commerce - 1962 - 732 lapas
...drug or employed as a control in the investigation. "d. The investigator is required to furnish his reports to the sponsor of the drug who is responsible...for collecting and evaluating the results obtained by various investigators. The sponsor is required to present progress reports at appropriate intervals...
Pilnskats - Par šo grāmatu

Recombinant DNA Research, 10. sējums

1986 - 652 lapas
...reference to the previous submission will be adequate). d. The investigator is required to furnish his reports to the sponsor of the drug who is responsible...for collecting and evaluating the results obtained by various investigators. The sponsor is required to present progress reports to the Food and Drug...
Pilnskats - Par šo grāmatu

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

1976 - 1046 lapas
...drug or employed as a control In the investigation. d. The Investigator is required to furnish his reports to the sponsor of the drug who is responsible...for collecting and evaluating the results obtained by various Investigators. The sponsor Is required to present progress reports to the Food and Drug...
Pilnskats - Par šo grāmatu

A Legislative History of the Federal Food, Drug, and Cosmetic Act and Its ...

1979 - 840 lapas
...drug or employed as a control In the investigation. d, The Investigator is required to furnish his reports to the sponsor of the drug who is responsible...for collecting and evaluating the results obtained by various investigators. The sponsor is required to present progress reports at appropriate Intervals...
Pilnskats - Par šo grāmatu

Pharmaceutical Innovation--promises and Problems: Hearing Before the ...

United States. Congress. House. Committee on Science and Technology. Subcommittee on Natural Resources, Agriculture Research, and Environment - 1982 - 252 lapas
...the drug or employed as a control in the investigation. d. The investigator is required to fumish his reports to the sponsor of the drug who is responsible...for collecting and evaluating the results obtained by various investigators. The sponsor is required to present progress reports to the Food and Drug...
Pilnskats - Par šo grāmatu

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

1985 - 982 lapas
...drug or employed as a control in the investigation. d. The investigator is required to furnish his reports to the sponsor of the drug who is responsible...for collecting and evaluating the results obtained by various investigators. The sponsor is required to present progress reports to the Food and Drug...
Pilnskats - Par šo grāmatu

The Code of Federal Regulations of the United States of America

1989 - 1022 lapas
...[52 PR 8831. Mar. 19. 1987. as amended at 52 FR 23031. June 17. 1987] § 312.64 Investigator reporte. (a) Progress reports. The investigator shall furnish...required under § 312.33 to submit annual reports to PDA on the progress of the clinical investigations. (b) Safety reports. An investigator shall promptly...
Pilnskats - Par šo grāmatu




  1. Mana bibliotēka
  2. Palīdzība
  3. Izvērstā grāmatu meklēšana
  4. Lejupielādējiet ePub
  5. Lejupielādēt PDF