USA – FDA Authorizes First Over-the-Counter At-Home Test to Detect Both Influenza and COVID-19...

Today, the U.S. Food and Drug Administration issued an emergency use authorization (EUA) for the first over-the-counter (OTC) at-home diagnostic test that can differentiate and detect...
Modalités pratiques de dépôt d'un dossier auprès de la CNEDiMTS

France – La HAS actualise la doctrine vaccinale de lutte contre les orthopoxvirus

Les orthopoxvirus constituent une famille de virus à laquelle appartiennent la variole, mais aussi la vaccine et le mpox (nouveau nom du virus monkeypox). Comme...

USA – Uptake of biosimilars on the rise in the US, but number of...

Fewer biosimilars have been marketed in the United States, compared with Germany and Switzerland, and prices are significantly higher in the US. However, biosimilars...

USA – FDA revises guidance on electronic systems and signatures in clinical trials

The US Food and Drug Administration (FDA) on Wednesday revised its draft guidance on electronic systems, records and signatures in clinical trials. While the...

Europe – GSK’s RSV vaccine candidate recommended by CHMP for older adults

There are currently no vaccines available to help protect older adults from RSV, a common contagious virus characterised by several mild, cold-like symptoms. Although...
New guidance on biologics affects authorized generics

USA – FDA officials tout steady growth in biosimilar program, enhancements under FDORA

US Food and Drug Administration (FDA) officials touted “steady growth” in the total number of biosimilar products since the program’s inception, with 40 approvals...

USA – FDA establishes advisory committee for genetic metabolic disease treatments

The Genetic Metabolic Diseases Advisory Committee will advise the FDA on products used for the diagnosis, prevention and treatment of genetic metabolic diseases under...

USA – FDA asks manufacturers to develop risk management plans to avert shortages

The US Food and Drug Administration (FDA) has issued draft guidance that spells out which types of drugs and medical devices are vulnerable to...
New guidance on biologics affects authorized generics

USA – FDA authorizes Pfizer, Moderna vaccines for youngest children

The US Food and Drug Administration (FDA) on Friday authorized the emergency use of Moderna and Pfizer-BioNTech’s COVID-19 vaccines for children as young as...

USA – FDA Says Face-to-Face Meetings Include Virtual

The FDA is changing its definition of face-to-face meetings to clarify that they include both in-person meetings and virtual meetings on audio- and video-enabled...