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 2017_register executive 2017-04-25 article Notices D09002ee1c7f1c6c8 D09002ee1c7f1c774 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 (FDA) Center for Drug Evaluation and Research (CDER), together with the Center for Devices and Radiological Health (CDRH), is sponsoring a 2-day public conference entitled "FDA Small Business and Industry Assistance Regulatory Education for Industry (REdI) Spring Conference." The goal of this public conference is to provide direct, relevant, and helpful information on the key aspects of drug and medical device regulations in order to increase regulatory certainty and predictability for pharmaceutical and/or medical device industry. Our primary audience is that of small manufacturers of drug and/or medical devices who want to learn about how FDA approaches the regulation of drugs and medical devices and for whom increased certainty and predictability will help to decrease the regulatory burdens that can be associated with a lack of understanding of, or familiarity with, FDA's drug and medical device regulations. However, anyone involved in the pharmaceutical and/or medical device industry may attend. 82 FR 19066 https://www.govinfo.gov/app/details/FR-2017-04-25/2017-08308 2017-08308 fr25ap17-75 4164-01-P Docket No. FDA-2017-N-0001 https://www.govinfo.gov/app/details/FR-2017-04-25/2017-08308 https://www.govinfo.gov/content/pkg/FR-2017-04-25/html/2017-08308.htm https://www.govinfo.gov/content/pkg/FR-2017-04-25/pdf/2017-08308.pdf 2 p. 19066 19067 82 FR 19066 Food and Drug Administration Small Business and Industry Assistance Regulatory Education for Industry Spring Conference; Public Conference; Federal Register Vol. 82, Issue NOTICE 2017-08308 DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration Docket No. FDA-2017-N-0001 4164-01-P 2017-08308 Notice of public conference.

The Food and Drug Administration (FDA) Center for Drug Evaluation and Research (CDER), together with the Center for Devices and Radiological Health (CDRH), is sponsoring a 2-day public conference entitled "FDA Small Business and Industry Assistance Regulatory Education for Industry (REdI) Spring Conference." The goal of this public conference is to provide direct, relevant, and helpful information on the key aspects of drug and medical device regulations in order to increase regulatory certainty and predictability for pharmaceutical and/or medical device industry. Our primary audience is that of small manufacturers of drug and/or medical devices who want to learn about how FDA approaches the regulation of drugs and medical devices and for whom increased certainty and predictability will help to decrease the regulatory burdens that can be associated with a lack of understanding of, or familiarity with, FDA's drug and medical device regulations. However, anyone involved in the pharmaceutical and/or medical device industry may attend.

The public conference will be held May 9 and 10, 2017, from 8:30 a.m. to 4:30 p.m. See the SUPPLEMENTARY INFORMATION section for registration information. Brenda Stodart, Center for Drug Evaluation and Research, Food and Drug Administration, 10001 New Hampshire Ave., Silver Spring, MD 20993-0002, 301-796-6707, email: cdersbia@fda.hhs.gov; or Elias Mallis, Center for Devices and Radiological Health, 10903 New Hampshire Ave., Silver Spring, MD 20993- 0002, 301-796-7100, email: DICE@fda.hhs.gov. Meetings: Food and Drug Administration Small Business and Industry Assistance Regulatory Education for Industry Spring Conference; Public Conference , cdersbia@fda.hhs.gov DICE@fda.hhs.gov info@sbiaevents.com https://collaboration.fda.gov/common/help/en/support/meeting_test.htm https://www.adobe.com/go/connectpro_overview https://www.fda.gov/Drugs/DevelopmentApprovalProcess/SmallBusinessAssistance/ucm545309.htm Vol. 82, no. 78 Office of the Federal Register, National Archives and Records Administration 2017-04-25 continuing daily deposited born digital 214 p. Table of Contents: AE 2.7: GS 4.107: AE 2.106: KF70.A2 https://www.govinfo.gov/app/details/FR-2017-04-25 P0b002ee194aae9fd 0097-6326 0042-1219 0364-1406 769-004-00000-9 000582072 f:fr25ap17 https://www.govinfo.gov/app/details/FR-2017-04-25 https://www.govinfo.gov/content/pkg/FR-2017-04-25/pdf/FR-2017-04-25.pdf https://www.govinfo.gov/content/pkg/FR-2017-04-25/xml/FR-2017-04-25.xml fdlp 18975 19178 DGPO 2017-04-25 2024-06-01 FR-2017-04-25 machine generated eng FR FR-2017-04-25 82 78