Regulations.gov document

M7(R1) Assessment and Control of DNA Reactive (Mutagenic) Impurities in Pharmaceuticals To…

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

Key facts

Document ID FDA-2018-D-0740-0002
Title M7(R1) Assessment and Control of DNA Reactive (Mutagenic) Impurities in Pharmaceuticals To Limit Potential Carcinogenic Risk Guidance for Industry
Document type Other
Subtype Guidance
Agency FDA
Docket FDA-2018-D-0740
Posted Mar 14, 2018
Comment period opens Mar 14, 2018

At a glance

  • None Public comments on this docket

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