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Other Post-market Vigilance data Footnote 6 (Undefined Data Post-market Vigilance (UDPV)) requested by MHPD Footnote 5.

Risk Management Plan (RMP), when provided to MHPD Footnote 5.Periodic Safety Update Report (PSUR) or Periodic Benefit Risk Evaluation Report (PBRER) when provided to the Marketed Health Products Directorate (MHPD) Footnote 5.Veterinary drug regulatory activities pursuant to Part C, Division 1 and Division 8 of the Food and Drug Regulations.Medical Device regulatory activities pursuant to sections 32 and 82 of the Medical Devices Regulations.Administrative Regulatory Activities pursuant to Part C, Division 8 of the Food and Drug Regulations.Drug Notification Forms (DNF) pursuant to Part C, Division 1 and Division 8 of the Food and Drug Regulations.Post-Notice of Compliance (NOC) Changes: Level III forms pursuant to Guidance Document: Post-Notice of Compliance (NOC) Changes: Framework Document.Developmental Safety Update Reports (DSUR).A human drug regulatory activity pursuant to Part C, Division 8 of the Food and Drug Regulations.A Clinical Trial involving human subjects pursuant to Part C, Division 5 of the Food and Drug Regulations.An application for Drug Identification Number (DIN) pursuant to Part C, Division 1 of the Food and Drug Regulations.