Brief

The document provides guidance for key stakeholders in the medicines supply chain. It aims to facilitate their use of the NIMAR regulatory route, enabling the continued supply of Great Britain (GB) licensed medicines to Northern Ireland (NI). This guidance is intended for industry and trade organizations, wholesalers, logistics providers, and healthcare professionals involved in the supply chain. The document's purpose is to inform stakeholders about the requirements and procedures for using the NIMAR regulatory route effectively.

This content is restricted.

Highlights content goes here...

This content is restricted.

Medicines and Healthcare products Regulatory Agency (MHRA)

Quick Insight
RADA.AI
RADA.AI
Hello! I'm RADA.AI - Regulatory Analysis and Decision Assistance. Your Intelligent guide for compliance and decision-making. How can i assist you today?
Suggested

Form successfully submitted. One of our GRI rep will contact you shortly

Thanking You!

Enter your Email

Enter your registered username/email id.

Enter your Email

Enter your email id below to signup.
Individual Plan
$125 / month OR $1250 / year
Features
Best for: Researchers, Legal professionals, Academics
Enterprise Plan
Contact for Pricing
Features
Best for: Law Firms, Corporations, Government Bodies