News

NHS Free Morning-After Pill Reaches 305,000 Women

In a major milestone in improving women’s reproductive healthcare, the NHS free morning-after pill program has enabled nearly 305,000 women in England …

Thyroid Medication Levothyroxine Recall: FDA Issues Alert Over Reduced Potency

The U.S. Food and Drug Administration (FDA) has announced a nationwide thyroid medication Levothyroxine recall on several sodium tablet products because they …

Health Advisory Panel Recommends Easing FDA Peptide Restrictions in USA

The FDA Pharmacy Compounding Advisory Committee meeting held on 23 and 24th July voted to allow several controversial peptides for inclusion on …

Eli Lilly Retatrutide Drug Trial Adds Two More Phase 3 Wins & Plans FDA Approval

Eli Lilly retatrutide drug trial has delivered more positive results from two additional Phase 3 studies in a late-stage clinical study. The …

FDA Approval for GSK’s Lung Cancer Drug: A Milestone In Oncology After Nuvalent Acquisition

The U.S. Food and Drug Administration (FDA) has officially approved a new lung cancer drug, Jideytro (zidesamtinib), by pharmaceutical giant GSK. This …

Trump’s Generic Drug Tariffs Could Affect U.S. Healthcare & Trade

President Donald Trump has announced a phased tariff schedule on imported low-cost medicines, introducing a two-year grace period before imposing dramatic tax …

Unique Pharmaceutical Cetirizine Pill Recall

The U.S. Food and Drug Administration (FDA) has announced a nationwide drug recall alerton the Cetirizine Hydrochloride Tablets by Unique Pharmaceutical Laboratories …

Qdenga Becomes India’s First Approved Dengue Vaccine: When Will It Be Available?

The Central Drugs Standard Control Organisation (CDSCO), under the supervision of the Drug Controller General of India (DCGI), has officially granted marketing …

DPH Confirms First Case Of Measles in Delaware in Over a Decade

The Delaware Division of Public Health (DPH) confirmed the state’s first case of measles in Delaware since 2014. The patient was identified …

Tempus AI Personalis Acquisition: $1.5B Deal to Expand Cancer Monitoring & MRD Testing

The precision medicine firm Tempus AI has announced a definitive agreement to acquire Personalis Biotech for approximately $1.5 billion. With the Personalis …

Bristol Myers Squibb and Nvidia Partnership Build AI Factory

Global biopharmaceutical leader Bristol Myers Squibb (BMS) has announced an expanded collaboration with technology giant NVIDIA. The Bristol Myers Squibb and NVIDIA …

FDA Approval For Merck's Cholesterol Pill

The U.S. Food and Drug Administration (FDA) has approved Merck’s cholesterol pill, Lipfendra (enlicitide). Lipfendra is the first-ever FDA-approved oral PCSK9 inhibitor. …