Bill of Health

MARCH 24, 2022

At the research and development (R&D) stage, government funders can bind producers to equity goals through targeted contractual provisions, as we explain in a recently-published Nature Biotechnology article. The first pathway is requiring funding recipients to use out-licensing to alleviate scarcity.

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COVID-19 Vaccine Licensing COVID-19 Public Health 130

Bill of Health

AUGUST 29, 2022

government funding, announced that it felt “a special obligation … to use our resources to bring this pandemic to an end as quickly as possible.” Monsanto and Myriad) ( this 2015 article discusses the history and taxonomy of patent pledges, many of which are collected in this online database ). By Jorge L. Pandemic Pledges.

COVID-19 Vaccine 362

COVID-19 Vaccine COVID-19 Licensing Governance 362

Healthcare IT Today

AUGUST 24, 2022

The first article in this series, Disabilities and Accessibility in Health IT: The Need Is Constant , introduced the importance of designing web sites and other health care tools for many different types of people. In this article, we’ll look at how far you can go with the automation of web site accessibility.

ADA 83

ADA Compliance Licensing World Health 83

SQA

FEBRUARY 15, 2023

A new template for the Certificate of a Pharmaceutical Product will be put into use in line with China’s pharmaceutical export practices and the latest World Health Organization (WHO) guidelines. The application/notification must be submitted via the EUDAMED database (Article 69 IVDR).

US Department of Health and Human Services 40

US Department of Health and Human Services FDA COVID-19 World Health 40

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

SQA

OCTOBER 18, 2022

Health Canada is warning consumers about counterfeit BTNX Rapid Response COVID-19 antigen rapid test kits (25-pack boxes) found in Ontario. The counterfeit devices were sold online by a distributor named Healthful Plus without the required license to import, distribute, or sell medical devices in Canada.

US Department of Health and Human Services 40

US Department of Health and Human Services FDA COVID-19 Compliance 40

SQA

FEBRUARY 26, 2024

” If the product is prohibited in Brazil, a notice of infraction is drawn up for smuggling of goods (Article 334 A, item II, of the Criminal Code), which is then sent to the Public Prosecutor’s Office for criminal investigation. ISO/IEC 42001 , the world’s first AI management system standard, meets that need.

FDA 52

FDA Compliance COVID-19 Public Health 52