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SQA Regulatory Surveillance Summary 3 | Monthly Update 2021

SQA

APRIL 30, 2021

726/2004, 09 March 2021. 726/2004 , which essentially means duplicate MAAs for products authorized via the centralized procedure. Russia – Ministry of Health of the Russian Federation. The Russian Government continues to take measures to increase the quality and accessibility of health care for all patients.

COVID-19 Vaccine 52
COVID-19 Vaccine COVID-19 Compliance Governance 52
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SQA Regulatory Surveillance Summary | Monthly Update 2023 – July and August 2023

SQA

OCTOBER 18, 2023

Time frame for Accepting CE Marked Medical Devices in Great Britain Extended, 01 July 2023 The United Kingdom (UK) government has made regulations ( The Medical Devices (Amendment) (Great Britain) Regulations 2023 ) that enable CE marked medical devices to be accepted in Great Britain for defined periods beyond 30 June 2023.

FDA 40
FDA Compliance Licensing World Health 40
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