Quality and compliance at the heart of our approach
Healthcare products require a structured approach to quality, documentation and regulatory compliance.
GLOBENCIA works with manufacturers and regulatory stakeholders to ensure that product introduction is approached in accordance with applicable Moroccan requirements.
Five structured steps
Product Assessment
Evaluation of the product, intended use, classification and available documentation.
Documentation
Review and coordination of technical, regulatory and quality documentation.
Regulatory Pathway
Assessment of applicable Moroccan requirements for the product category.
Market Preparation
Preparation of the product for appropriate commercial introduction.
Ongoing Monitoring
Continuous attention to product information, market feedback and applicable requirements.
Important statement
GLOBENCIA is committed to responsible healthcare distribution and to complying with applicable laws, regulations and regulatory requirements.
The information published on this website is provided for general and professional information purposes. It in no way replaces the manufacturer’s insert, the advice of a healthcare professional, or the decisions of the competent authorities.
Interested in entering the Moroccan market?
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