Guidance Document: Regulatory requirements for Drug Identification Numbers (DINs) - Summary
When Health Canada authorizes a drug to be marketed in Canada, a Drug Identification Number (DIN) is issued to the manufacturer and printed on the package labels. A DIN indicates that the evaluation of the drug determined that it met the relevant requirements of the Food and Drugs Act and its regulations and the drug has a favourable risk/benefit profile. Manufacturers of prescription and non-prescription drugs must obtain a DIN before they are marketed in Canada
- Publisher - Current Organization Name: Health Canada
- Licence: Open Government Licence - Canada
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Guidance Document: Regulatory requirements for Drug Identification Numbers (DINs) - SummaryHTMLEnglish publication HTML
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Guidance Document: Regulatory requirements for Drug Identification Numbers (DINs) - SummaryHTMLFrench publication HTML
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