United States Government Publishing Office publisher pbl distributor dst United States National Archives and Records Administration Office of the Federal Register author aut Government Organization text government publication eng FR Regulatory Information 2016_register executive 2018-02-02 article Notices D09002ee1c7f69478 D09002ee1c7f69517 United States Department of Health and Human Services originator org United States Government Agency or Subagency United States Food and Drug Administration originator org United States Government Agency or Subagency The Food and Drug Administration's (FDA's) Center for Drug Evaluation and Research (CDER) is announcing the continuation of the Regulatory Project Management Site Tours and Regulatory Interaction Program (the Site Tours Program). The purpose of this document is to invite pharmaceutical companies interested in participating in this program to contact CDER. 81 FR 6867 https://www.govinfo.gov/app/details/FR-2016-02-09/2016-02515 2016-02515 fr09fe16-78 4164-01-P Docket No. FDA-2014-N-0179 https://www.govinfo.gov/app/details/FR-2016-02-09/2016-02515 https://www.govinfo.gov/content/pkg/FR-2016-02-09/html/2016-02515.htm https://www.govinfo.gov/content/pkg/FR-2016-02-09/pdf/2016-02515.pdf 1 p. 6867 6867 81 FR 6867 Training Program for Regulatory Project Managers; Information Available to Industry; Federal Register Vol. 81, Issue NOTICE 2016-02515 DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration 2016-04-11 Docket No. FDA-2014-N-0179 4164-01-P 2016-02515 Notice.

The Food and Drug Administration's (FDA's) Center for Drug Evaluation and Research (CDER) is announcing the continuation of the Regulatory Project Management Site Tours and Regulatory Interaction Program (the Site Tours Program). The purpose of this document is to invite pharmaceutical companies interested in participating in this program to contact CDER.

Pharmaceutical companies may submit proposed agendas to the Agency by April 11, 2016. Dan Brum, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 22, Rm. 5480, Silver Spring, MD 20993-0002, 301-796-0578, dan.brum@fda.hhs.gov. Information Available to Industry: Training Program for Regulatory Project Managers , dan.brum@fda.hhs.gov Vol. 81, no. 26 Office of the Federal Register, National Archives and Records Administration 2016-02-09 continuing daily deposited born digital 290 p. Table of Contents: AE 2.7: GS 4.107: AE 2.106: KF70.A2 https://www.govinfo.gov/app/details/FR-2016-02-09 P0b002ee1983474fe 0097-6326 0042-1219 0364-1406 769-004-00000-9 000582072 f:fr09fe16 https://www.govinfo.gov/app/details/FR-2016-02-09 https://www.govinfo.gov/content/pkg/FR-2016-02-09/pdf/FR-2016-02-09.pdf https://www.govinfo.gov/content/pkg/FR-2016-02-09/xml/FR-2016-02-09.xml fdlp 6745 7024 DGPO 2018-02-02 2024-06-02 FR-2016-02-09 machine generated eng FR FR-2016-02-09 81 26