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Top News In Quality Systems Compliance Today - Breaking & Trending Today

Circumstances For Delaying Denying Limiting Or Refusing An FDA Inspection

Delaying, denying, limiting, or refusing a drug or device inspection without a reasonable justification will result in a less than collegial. ....

Mark Durivage , Quality Systems Compliance , Constitute Delaying , Device Inspection Revision , Drug Inspection ,

FDA Seeks Comment On Considerations For Externally Controlled Trials For Drugs Biologics

On Feb. 1, 2023, the FDA released a new guidance, "Considerations for the Design and Conduct of Externally Controlled Trials for Drug and. ....

Dianne Paraoan , Mark Durivage , Office Of Communication , Drug Administration , Quality Systems Compliance , Externally Controlled Trials , Dockets Management Staff ,

FDA Seeks Comment On Circumstances For Delaying Denying Limiting Or Refusing An Inspection

The FDA has released for public comment a proposed draft guidance, Circumstances that Constitute Delaying, Denying, Limiting, or Refusing a Drug or. ....

Mark Durivage , Drug Administration Safety , Health Administration , Office Of Strategic Planning , Drug Administration , Office Of Regulatory Affairs , Quality Systems Compliance , Constitute Delaying , Device Inspection Revision , Drug Inspection , Innovation Act , Occupational Safety , Dockets Management , Regulatory Affairs , Strategic Planning , Operational Policy ,

FDA Seeks Comment On Conducting Remote Regulatory Assessments

The FDA believes the use of both voluntary and mandatory remote regulatory assessments (RRAs) for all types of FDA-regulated products is in the. ....

Mark Durivage , Office Of Strategic Planning , Drug Administration , Quality Systems Compliance , Office Of Regulatory Affairs , Foreign Supplier Verification Program , Inspectional Observations , Dockets Management Staff , Regulatory Affairs , Strategic Planning , Operational Policy ,

FDA Seeks Comment On Conducting Remote Regulatory Assessments

The FDA believes the use of both voluntary and mandatory remote regulatory assessments (RRAs) for all types of FDA-regulated products is in the. ....

Mark Durivage , Office Of Strategic Planning , Drug Administration , Quality Systems Compliance , Office Of Regulatory Affairs , Foreign Supplier Verification Program , Inspectional Observations , Dockets Management Staff , Regulatory Affairs , Strategic Planning , Operational Policy ,