1+ day, 18+ hour ago  (1699+ words) This is interesting: conservative outlets are reporting that the FDA could complete its so-called "safety review" of mifepristone before the midterms. The Trump administration has been slow-walking this bogus study for nearly a year'deliberately avoiding any big public moves against…...

6+ day, 2+ hour ago  (284+ words) Arre bhai, Jackson Laboratories ke Punjab aur Himachal Pradesh mein bane factory ka license cancel ho gaya hai. Rajasthan mein maternal deaths ke baad yeh oxytocin injection ki jaanch mein galat paya gaya. WHO bhi peecha kar raha hai. Isse…...

6+ day, 7+ hour ago  (267+ words) New Delhi, June 26: The Ministry of Health and Family Welfare has published a draft notification proposing amendments to Rule 31 of the Drugs Rules, 1945, with the objective of rationalising the residual shelf-life requirement for imported drugs and further promoting Ease of…...

6+ day, 13+ hour ago  (274+ words) New Delhi [India], June 26: The Union Ministry of Health and Family Welfare has published a draft notification proposing amendments to Rule 31 of the Drugs Rules, 1945, with the objective of rationalising the residual shelf-life requirement for imported drugs and further promoting…...

1+ week, 3+ hour ago  (563+ words) A few members of Congress have been told to expect the Food and Drug Administration's safety review of the dangerous and deadly abortion pill mifepristone to be completed by September. The review is assessing data on mifepristone to determine whether…...

1+ week, 12+ hour ago  (422+ words) The Clinical Trial Vanguard FDA Backs Entera Bio's Phase 3 Plan for Oral EB613 Osteoporosis Drug Roughly 80 percent of postmenopausal women with severe osteoporosis who qualify for anabolic therapy never receive it, not because the drugs fail, but because every approved anabolic…...

1+ week, 5+ day ago  (229+ words) Background Osteoporotic fractures impose a substantial economic burden in the United States. Although multiple pharmacologic therapies reduce fracture risk, variation exists in prescribing patterns. Internal organizational data from our institution demonstrated disproportionate utilization of denosumab compared with zoledronic acid despite…...

1+ week, 6+ day ago  (319+ words) My job is to be a guardian of patient safety. As Safety Science Director, she works across both early development and post-marketing, ensuring that risks are anticipated, analyzed, and managed so treatments can reach patients responsibly. That attention does not…...

1+ week, 6+ day ago  (194+ words) A new scholarship opportunity is now available through partnership with the State of Iowa HHS for local businesses interested in becoming certified in radon services. This program offers reimbursement for individuals seeking to become a radon mitigation specialist, measurement specialist,…...

2+ week, 2+ day ago  (285+ words) The trial will randomise 150 adults with active axial spondyloarthritis to receive 400mg vilamakitug or placebo. XBiotech is set to go ahead with patient enrolment for the V-SPINE (PT064) Phase II clinical trial to assess the safety and efficacy of vilamakitug in adults…...