Pharmaceutical & Medtech Branding Resource Center
Guidance
- Tip Sheet: Navigating the Processes and Pitfalls of Drug Naming
- Tip Sheet: Guide to Successful Drug Naming
FDA Resources
- Best Practices in Developing Proprietary Names for Drugs
- Nonproprietary Naming of Biological Products
- Contents of a Complete Submission for the Evaluation of Proprietary Names
- Proprietary Name Review for Biologic Products
EMA Resources
- Guideline on the acceptability of names for human medicinal products processed through the centralized procedure
- Committee for Medicinal Products for Human Use (CHMP) meeting dates 2019-2021
- Invented Name Review Group (NRG) Mandate, Objectives and Rules of Procedure
- Pre-Authorisation Guidance – Product Name, Product Information and Prescription Status
