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After the Himachal Pradesh Drug Regulatory Authority received information about some infamous activities, a pharmaceutical company in the state has come under scrutiny.
U.S. Department of Justice announced that Bayer AG had reached an agreement to pay $40 million to resolve claims that it used kickbacks and made false statements about three prescription drugs.
USFDA has authorised the use of Orkambi (lumacaftor/ivacaftor) in children with cystic fibrosis (CF) who are homozygous for the F508del mutation (F/F genotype) and are between the ages of 12 and 24 months.
Frontline nonsquamous non-small cell lung cancer patients treated with Merck’s Keytruda had a five-year survival rate of 19.4%, compared to a 5% five-year survival rate with chemotherapy in the past.
USFDA has granted IND approval to Aston Sci. Inc., a clinical stage biopharmaceutical company specialising in the clinical development of therapeutic cancer vaccines, for AST-301, its flagship product, for a phase 2 clinical trial.
Phase 3 data on the topical ED treatment MED3000 from Futura Medical have been released, paving the way for the company to request FDA approval of the treatment as an over-the-counter drug by the end of the month.
The establishment of a bulk drug park in
Jambusar has received preliminary approval
in Gujarat, and the state’s pharmaceutical
industry anticipates that the park will be
operational in three years.
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