Tap any paragraph to write a margin note. Your notes collect in the Desk below the text and file under cases with @. The side-by-side margin rail opens on a larger screen.

Code · STATUTE-COMPILATIONS · FDA Reauthorization Act of 2017 · Sec. 205

Sec. 205. CONFORMITY ASSESSMENT PILOT PROGRAM

676 words·~3 min read·/statute-compilations/comps-15234/sec-205

A research copy — for the controlling text, always check the official state or federal source. Not legal advice.

## SEC. 205 CONFORMITY ASSESSMENT PILOT PROGRAM ###
(a)In general Section 514 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 360d) is amended by adding at the end the following: > > ### “(d) Pilot Accreditation Scheme for Conformity Assessment > > > #### “(1) In general > > The Secretary shall establish a pilot program under which— > > > ##### “(A) > > testing laboratories may be accredited, by accreditation bodies meeting criteria specified by the Secretary, to assess the conformance of a device with certain standards recognized under this section; and > > > ##### “(B) > > subject to paragraph (2), determinations by testing laboratories so accredited that a device conforms with such standard or standards shall be accepted by the Secretary for purposes of demonstrating such conformity under this section unless the Secretary finds that a particular such determination shall not be so accepted. > > > #### “(2) Secretarial review of accredited laboratory determinations > > The Secretary may— > > > ##### “(A) > > review determinations by testing laboratories accredited pursuant to this subsection, including by conducting periodic audits of such determinations or processes of accredited bodies or testing laboratories and, following such review, taking additional measures under this Act, such as suspension or withdrawal of accreditation of such testing laboratory under paragraph (1)(A) or requesting additional information with respect to such device, as the Secretary determines appropriate; and > > > ##### “(B) > > if the Secretary becomes aware of information materially bearing on safety or effectiveness of a device assessed for conformity by a testing laboratory so accredited, take such additional measures under this Act as the Secretary determines appropriate, such as suspension or withdrawal of accreditation of such testing laboratory under paragraph (1)(A), or requesting additional information with regard to such device. > > > #### “(3) Implementation and reporting > > > ##### “(A) Public meeting > > The Secretary shall publish in the Federal Register a notice of a public meeting to be held no later than September 30, 2018, to discuss and obtain input and recommendations from stakeholders regarding the goals and scope of, and a suitable framework and procedures and requirements for, the pilot program under this subsection. > > > ##### “(B) Pilot program guidance > > The Secretary shall— > > > ###### “(i) > > not later than September 30, 2019, issue draft guidance regarding the goals and implementation of the pilot program under this subsection; and > > > ###### “(ii) > > not later than September 30, 2021, issue final guidance with respect to the implementation of such program. > > > ##### “(C) Pilot program initiation > > Not later than September 30, 2020, the Secretary shall initiate the pilot program under this subsection. > > > ##### “(D) Report > > The Secretary shall make available on the internet website of the Food and Drug Administration an annual report on the progress of the pilot program under this subsection. > > > #### “(4) Sunset > > As of October 1, 2022— > > > ##### “(A) > > the authority for accreditation bodies to accredit testing laboratories pursuant to paragraph (1)(A) shall cease to have force or effect; > > > ##### “(B) > > the Secretary— > > > ###### “(i) > > may not accept a determination pursuant to paragraph (1)(B) made by a testing laboratory after such date; and > > > ###### “(ii) > > may accept such a determination made prior to such date; > > > ##### “(C) > > except for purposes of accepting a determination described in subparagraph (B)(ii), the Secretary shall not continue to recognize the accreditation of testing laboratories accredited under paragraph (1)(A); and > > > ##### “(D) > > the Secretary may take actions in accordance with paragraph
(2)with respect to the determinations made prior to such date and recognition of the accreditation of testing laboratories pursuant to determinations made prior to such date.” > .
Connectionstraces to 1
Traces to 1 document
Citation graph
cites case law
Sec. 205
CONFORMITY ASSESSMENT PILOT PROGRAM
Cites 1Cited by 0 across 0 sources
★   the supreme law of the land   ★
Don't Tread on Me
E Pluribus Unum — out of many, one

"If you don't know your rights, you don't have any."

Marginalia · a citizen's law index
A research desk, not legal advice. Always read the cited source before relying on a summary.
Questions or an issue? support@self-law.org
disclaimerMarginalia is a research index, not a law firm. Nothing on this site is legal, tax, or financial advice and no attorney–client relationship is formed by using it. Statutes, regulations, and case law change; summaries, search results, AI output, and member posts may be incomplete, out of date, or wrong. Any interpretation drawn from material on this site should be validated by a licensed attorney in your jurisdiction before you act on it.