Appendix B, Glossary and Acronyms
Glossary
Term used in this document | Definition of Term |
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Identification of Medicinal Products (IDMP) | Identification of Medicinal Products (IDMP) is a set of five ISO norms, which has been developed in response to a worldwide demand for internationally harmonized specifications for medicinal products. |
European Directorate for the Quality of Medicines and Healthcare (EDQM) | The European Directorate for the Quality of Medicines & Healthcare publishes a database of standard terms, for dose forms, routes of administration and various other key concepts within the domain. This was originally in response to a request from the European Commission, but now is available for wider global use to support the Identification of Medicinal Products (IDMP) initiative and to support healthcare generally. |
Health Canada Drug Product Database (DPD) | The DPD contains product specific information on drugs approved for use in Canada. The database is managed by Health Canada and includes human pharmaceutical and biological drugs, veterinary drugs, radiopharmaceutical drugs and disinfectant products. |
International Nonproprietary Names (INN) | International Nonproprietary Names (INN) are managed by the World Health Organization (WHO) and can be used to identify pharmaceutical substances that are acting as active pharmaceutical ingredients. Each INN is a unique name that is globally recognized and is public property, and therefore can be used freely. The INN is also intended to be used as a basis for non-branded product names in healthcare, to provide clear identification of medicines, safe prescription and dispensing of medicines to patients, and for communication and exchange of information among health professionals and scientists worldwide. |
Modified International Nonproprietary Names (INNm) | An INN is usually authored for the active part of the molecule only, to avoid the multiplication of entries in cases where several salts, esters, etc. are actually used in medicinal products. To describe active ingredient substances precisely, modified INNs (INNMs) must be created independently (e.g. within a terminology itself).
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Manufactured item | A “manufactured item” (in ISO 11615) is the entity that describes the qualitative and quantitative composition of a product that is contained in the packaging of a Medicinal Product – so it is the entity that has the Substance-Strength Set and a Dose Form |
Acronyms
Acronym | English Description | French Acronym | French Description |
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CCDD | Canadian Clinical Drug Data Set | RCM | Répertoire canadien des médicaments |
TM | Therapeutic Moiety | FT | Fraction thérapeutique |
NTP | Non-proprietary Therapeutic Product | PTC | Produit thérapeutique commun |
MP | Manufactured Product | PM | Produit manufacturé |
DIN | Drug Identification Number | DIN | Numéro d'identification d'un médicament |
DPD | Drug Product Database | BDPP | Base de données sur les produits pharmaceutiques |
LNHPD | Licensed Natural Health Products Database | BDPSNH | Base de données des produits de santé naturels homologués |
NPN | Natural Product Number | NPN | Numéro de produit naturel |
INN | International Nonproprietary Name | DCI | Dénomination commune internationale |
USAN | United States Adopted Names | USAN | dénomination commune américaine |
EDQM | European Directorate for the Quality of Medicines | DEQM | Direction européenne de la qualité du médicament |
IDMP | Identification of Medicinal Products | IDMP | Identification des produits médicaux |
EMR | electronic medical record | DSE | dossier de santé électronique |