FDA approves Sanofi biosimilar product for treatment of diabetes
The U.S. Food and Drug Administration approved Merilog as biosimilar to Novolog for the improvement of glycemic control in adults and pediatric ...
Penn State Extension to host FSMA Produce Grower Certification course
Penn State Extension will offer a course to help produce growers meet food safety rules as outlined in the Food Safety Modernization Act, also known as FSMA, administered by the U.S. Food and Drug ...
The Statesman15d
U’khand govt denies reports of mandatory religious certificates for live-in relationship registration
The Uttarakhand government on Thursday denied reports that the Uniform Civil Code mandates clergy permission for registration ... reports of mandatory religious certificates under UCC for all ...
Daily16d
CPS Mumbai Urges State Medical Councils to Verify Certificates Before Granting Additional Qualification Registration
In this regard, CPS has written a letter to all the state medical councils requesting them to send a copy of the certificates of the students coming for additional qualification to CPS for ...
Hosted on MSN16d
Dropping of Dengvaxia cases lauded
Former health secretary Janette Garin, who was involved in the Dengvaxia vaccine anomaly, said the Department of Justice's (DOJ) move to withdraw 98 criminal cases related to the vaccination ...
Sun Star21d
FDA warns public against unregistered dried mango product
THE Food and Drug Administration (FDA) warned the public on Friday, January 24, 2025, about the presence of an unregistered dried mango product on the market.In ...
NBC News23d
Federal regulations paused, halting FDA's proposed ban on formaldehyde in hair products
Not all chemical hair relaxers include the chemical, but many include ingredients that can release formaldehyde when heated, the FDA said in 2024. Over the years, an increasing number of studies ...
Newsweek23d
FDA Approves Nasal Spray for Depression
However, it had to be used in conjunction with an oral medication. The FDA has now expanded its approval to include the standalone use of the nasal spray for adults with treatment-resistant major ...
CNN23d
FDA approves standalone use of J&J’s ketamine-derived depression treatment
The U.S. Food and Drug Administration expanded approval for Johnson & Johnson’s nasal spray, Spravato, to allow it to be used as a standalone treatment for patients with severe depression, the ...
Popular Science24d
FDA approves first-of-its-kind nasal spray for severe depression
Johnson & Johnson has announced the FDA’s approval of a first-of-its-kind, esketamine nasal spray called Spravato for the standalone treatment of major depressive disorder (MDD), PTSD ...
Medical Design and Outsourcing24d
Cortland Biomedical secures FDA registration
Cortland, New York – Cortland Biomedical, a full-service biomedical textile product development partner that provides access to a full spectrum of global engineering, design, and manufacturing ...