SQA

MAY 24, 2023

As recommended by the International Health Regulations (IHR), there must be a vector-free zone at seaports, airports, and land crossing and within a perimeter of 400 meters around these entry points. For this, it is necessary to maintain regular active surveillance and vector control so that the risk of disease transmission is reduced.

FDA 40

FDA Licensing Governance Compliance 40

SQA

SEPTEMBER 2, 2022

Affected manufacturers have until 28 November 2022 to comply with the ANVISA BGMP certification requirements. On 09 May 2022, NMPA released the draft of the revised Regulations for Implementation of the Drug Administration Law (hereafter referred to as the Regulations ) for public comments. effective as of 01 July 2023.

FDA 91

FDA COVID-19 Nursing Homes Compliance 91

SQA

DECEMBER 10, 2021

Brazil’s New UDI Requirements for Medical Devices: Compliance Implications for Manufacturers, 02 August 2021. According to ANVISA Public Consultation 1051/2021 , the regulator plans a six-year rollout of UDI requirements in order to boost traceability and monitoring of medical devices and equipment commercialized in Brazil.

FDA 52

FDA Compliance Public Health Hospitals 52

SQA

FEBRUARY 26, 2024

The action was held from 26 to 28 September 2023, at the city’s international entry points. The products found, subject to retention and seizure, were retained by the Federal Revenue Service. The 2023 resolutions, RE nº 3,770 and nº 3,771 , cover several of these companies’ products.

FDA 52

FDA Compliance COVID-19 Public Health 52