bilingual labelling

Regulatory Framework for Licensing Contraceptive Medical Devices in Canada

15

Jul

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Medical Devicesbilingual labelling, Class II devices, Class III devices, clinical evidence, contraceptive medical devices, health canada, ISO 13485, Medical Device Licence, post-market surveillance

Regulatory Framework for Licensing Contraceptive Medical Devices in Canada

The licensing pathway for contraceptive products in Canada can be complex, particularly for manufacturers and importers aiming to introduce new products or expand existing lines. One of the main challenges is the lack of clear, consolidated guidance that explains how different types of contraceptives are regulated under Canadian law. Hormonal…

A Cost-Effective Compliance Strategy: Over-labelling for Packaging in the Canadian Market

Expanding into the Canadian food and natural health product market presents a unique set of regulatory challenges. From bilingual packaging requirements to specific nutrition facts and allergen declarations, manufacturers often face barriers that can delay product launches and increase operational costs. One practical and cost-effective solution to this issue is…

2025 Overview of Natural Health Product (NHP) Regulations and NPN Licensing in Canada

Navigating the complex and ever-evolving landscape of Natural Health Product (NHP) Regulations in Canada is crucial for businesses hoping to enter the Canadian market. Canada offers a significant market opportunity for companies, similar to the U.S., but success depends on a thorough understanding of the regulatory requirements. Ensuring compliance with…