Questions and Answers: Plain Language Labelling Regulations for Prescription Drugs - document

This document provides information for industry on how Health Canada's Health Products and Food Branch interprets and applies the 2014 Regulations Amending the Food and Drug Regulations (Labelling, Packaging and Brand Names of Drugs for Human Use) for prescription products and those administered or obtained through a health professional. Please note that this includes prescription pharmaceutical drugs, biologic drugs (Schedule D), and radiopharmaceuticals (Schedule C).

Data and Resources

Additional Info

Field Value
Source
Version
Author
Author Email
Maintainer
Maintainer Email
Data Level
Agreement Required
Purpose Constraints
Redistribution Allowed
AI Training Allowed
Data Steward
Title (French) Questions-réponses : Le règlement sur l’étiquetage en langage clair pour les médicaments sur ordonnance - document
Update Frequency as_needed
Geographic Scope []
Criticality Level []
Sensitivity Level unrestricted
Language
Contact Person
Contact Email
Data Dictionary
Open Canada Date Published 2020-05-14 00:00:00
Open Canada Date Modified
Open Canada Subject ["health_and_safety"]
Open Canada Keywords {"fr": ["questions et réponses", "règlements sur l'étiquetage en langage clair", "médicaments sur ordonnance", "étiquetage", "emballage et noms de marque des médicaments", "médicaments à usage humain", "médicaments pharmaceutiques sur ordonnance", "médicaments biologiques", "annexe-D", "produits radiopharmaceutiques", "annexe-C"], "en": ["questions and answers", "plain language labelling regulations", "prescription drugs", "labelling", "packaging and brand names of drugs", "drugs for human use", "prescription pharmaceutical drugs", "biologic drugs", "schedule-D", "radiopharmaceuticals", "schedule-C"]}
Open Canada Collection publication
Principal Organization
Reference Data
Official Source