MHRA definition

MHRA means the Medicines and Healthcare products Regulatory Agency;
MHRA means the United Kingdom’s Medicines and Healthcare products Regulatory Agency and any successor agency(ies) or authority having substantially the same function.
MHRA means the Medicines and Healthcare products Regulatory Agency.

Examples of MHRA in a sentence

  • All Registrations from the FDA, TGA, MHRA, Medsafe and EMA in respect of the Products shall be valid and subsisting and in full force and effect.

  • To the knowledge of Borrower and its Subsidiaries, neither FDA, EMA, TGA, MHRA, Medsafe, nor any comparable Governmental Authority is considering limiting, suspending, or revoking such Registrations.


More Definitions of MHRA

MHRA means the Medicines and Healthcare products Regulatory Agency in the United Kingdom.
MHRA means the Medicines and Healthcare products Regulatory Agency; "Mid-Point Date" for each Good in each of the Supplier Lots specified in the Award Schedule, means the date falling half way between the Commencement Date and the expiry date specified in the Award Schedule for that Good;
MHRA means the Medicines and Healthcare products Regulatory Agency that regulates medicinal products, medical devices and blood components for transfusion in the U.K.
MHRA means The Medicines and Healthcare products Regulatory Agency, an executive agency of the Department of Health and Social Care in the United Kingdom which is responsible for ensuring that medicines and medical devices work and are acceptably safe.
MHRA means the Medicines and Healthcare Products Regulatory Agency of the UK’s Department of Health, or any successor organization.
MHRA is defined in Section 1.177 (Definition of Regulatory Authority).
MHRA means the Medicines and Healthcare Products Regulatory Agency, or any successor thereto, having the administrative authority to regulate the marketing of in vitro diagnostics and other medical devices in the United Kingdom.