NHRA MDR Transition Guideline: Overview
The article describes in detail the transitional arrangements associated with the recent regulatory changes in the European Union.
The article describes in detail the transitional arrangements associated with the recent regulatory changes in the European Union.
The article provides an overview of the regulatory requirements for custom-made medical devices intended to be used in Bahrain and also describes in detail the documentation to be submitted by an interested party when applying for marketing approval. Table of Contents...
The new article describes in detail the process of applying for importation approval for a medical device. Table Of Contents: The National Health Regulatory Authority (NHRA), a Bahrain’s regulatory agency in the sphere of healthcare products, has published a guidance...
The new article highlights the aspects related to building in the context of applications for marketing approval. Table Of Contents: The National Health Regulatory Authority (NHRA), a Bahrain’s regulatory agency in the sphere of healthcare products, has published a...
The new article addresses the aspects related to possible changes to an existing license, including the transferring local representative, renewal, and manufacturer acquisition. Table Of Contents: The National Health Regulatory Authority (NHRA), a Bahrain’s agency...