Regulations.gov document

M7(R1): Assessment and Control of Deoxyribonucleic Acid Reactive (Mutagenic) Impurities in…

Notice · FDA-2018-D-0740 · posted Mar 14, 2018

Key facts

Document ID FDA-2018-D-0740-0001
Title M7(R1): Assessment and Control of Deoxyribonucleic Acid Reactive (Mutagenic) Impurities in Pharmaceuticals To Limit Potential Carcinogenic Risk; Guidance for Industry; Availability
Document type Notice
Subtype Notice of Availability
Agency FDA
Docket FDA-2018-D-0740
Posted Mar 14, 2018
Federal Register citation 83 FR 11210
FR document number 2018-05118
Comment period opens Mar 14, 2018
Effective date Mar 14, 2018

At a glance

  • 1–9 Pages
  • None Public comments on this docket

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