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The terms regarding Windsor Framework that you need to know are here:

 

EMVS

European Medicines Verification System

 

PL

A product licensed by the MHRA that covers the whole of the UK, coming into effect from 1 January 2025

 

UK-wide Marketing Authorization (MA)

A product licensed by the MHRA, across the whole of the UK, before 1 January 2025

 

PLNI

A product licensed by the MHRA that covers Northern Ireland (NI) only as the territorial application

 

PLGB

A product licensed by the MHRA that covers Great Britain (GB) only as the territorial application

 

NIMAR

Northern Ireland MHRA Authorized Route

 

eCTD

Electronic Common Technical Document

 

MAA

Marketing Authorization Applications

 

THR

Traditional Herbal Medicinal Product

 

HR/NR

Homeopathic Medicinal Product

 

PLPI

Parallel Imports

 

Union Authorization

A marketing authorization issued by the European Commission for a product approved through the European Medicines Agency (EMA) centralized procedure

 

Centrally Authorized Product (CAP)

A medicinal product authorized through a Union Authorization issued by the European Commission and valid across the European Union

 

CMA

Conditional Marketing Authorization

 

QP

Qualified Person

 

RP

Responsible Person

 

RPi

Responsible Person for Import