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Found 10 records similar to Licensed Natural Health Products Database (LNHPD)
Unfortunately, the text-based data extract is no longer accessible through the Natural and Non-prescription Health Products (NNHPD) website. We want to underline that the support for the CSV (text) extract formats has been dropped by our program area and the links to CSV files on the page will be deleted soon. However, the alternative formats XML and JSON are both available and are updated daily and will continue to be moving forward. .For the most recent LNHPD extract you can retrieve either XML or JSON extracts from our API.
This guide was developed to help users search and navigate the Natural Health Products Ingredients Database using the online Web application.
This document describes the use of the Natural Health Products Ingredients Database Issue Form, which is designed to help applicants send NHPID data requests which are complete and accurate.
The Natural Health Products Ingredients Database is a repository of scientific terminologies and Pre-cleared Information approved by the Natural and Non-prescription Health Products Directorate (NNHPD).
The objective of this document is to provide guidance on the standards and terminologies to facilitate the exchange and practical use of natural health product information by the Natural Health Products (NHP) Online System.
The Natural Health Products (NHP) Online System is a suite of secure web applications and tools that you can use to fill your NHP licence application.
This guidance document provides information to help product licence applicants determine the evidence (type and amount of data) to provide as part of a product licence application to support the safety (risk) and efficacy (benefit) of natural health products (NHPs) that make modern health claims.
The Amendment and Notification Form (ANF) is the exclusive form to be used for submitting post licensing changes for a licensed natural health product (NHP) to the Natural and Non-prescription Health Products Directorate (NNHPD).
The site licensing system requires that all manufacturers, packagers, labellers, and importers be licensed. Sites must have procedures in place for distribution records and product recalls and for the handling, storage and delivery of their products. They must also demonstrate that they meet good manufacturing practice requirements.
This guide is for anyone working with drugs or natural health products. It will help facilitate understanding and compliance with sections of the Food and Drugs Act (the Act), the Food and Drug Regulations (FDR) and Natural Health Products Regulations (NHPR) that relate to recalls.