Public consultation open on guideline on the acceptability of names for human medicines
The European Medicines Agency has released the sixth revision of the guideline on the acceptability of names for human medicinal products processed through the centralised procedure for public consultation.
The current update of this guideline provides further recommendations on the requirements for acceptability and submission of proposed (invented) names.
It also clarifies:
- specific aspects of the criteria applied to address safety and public-health concerns;
- international-non-proprietary-name issues;
- product-specific concerns;
- the procedure for submission of proposed (invented) name requests.
How useful is this page?
Average rating:Based on 9 ratings
Add your rating:
- See all ratings
8 ratings0 ratings0 ratings1 ratings0 ratings