US Food and Drug Administration (FDA) and Drug Enforcement Administration (DEA), the agencies came to together to warn four online networks operating 10 websites that illegally market unapproved and misbranded versions o... Read More
The U.S.Food and Drug Administration has affirmed rituximab (Rituxan, Genentech) for the treatment of granulomatosis with polyangiitis (GPA, or also called as Wegener’s) and microscopic polyangiitis (MPA) in childr... Read More
The U.S. Food and Drug Administration today extended the endorsement of Mavyret (glecaprevir and pibrentasvir) tablets for an eight-week term for the treatment of grown-ups and kids ages 12 years and more seasoned or wei... Read More
The approval of Jynneos Smallpox and Monkeypox Vaccine, Live, Non-Replicating, for the prevention of smallpox and monkeypox disease in adults (18 years of age and older) determined to be at high risk for smallpox or monk... Read More
The US Food and Drug Administration (FDA) is warning healthcare professionals and patients of a review of 14 bunches of ranitidine capsules appropriated by Sandoz Inc, the biosimilars and generics unit of Swiss pharma ma... Read More
Merck’s revered checkpoint inhibitor Keytruda grabbed another administrative endorsement. The U.S. Nourishment and Drug Administration (FDA) affirmed Keytruda in blend with Eisai’s Lenvima for the treatment o... Read More
Salmonella bacteria were found by the U.S. Food and Drug Administration (USFDA) in three batches of MDH’s sambar masala. The USFDA said in a release that lot code 108, 47 and 48 are the three lots which have been m... Read More
Federal health officials have learned that Sanofi’s heartburn medication Zantac includes an impurity that could cause cancer, the U.S. Food and Drug Administration said Friday. The probe comes after Valisure, an online... Read More
Juul Company was slammed by Federal health officials for illegally advertising its nicotine pods as a safer alternative to cigarettes, threatening to fine or even seize the company‟s products if it doesn‟t correct it... Read More
The US Food and Drug Administration (FDA) warned Indian generic drugmaker Strides Pharma earlier this month over good manufacturing practice (GMP) violations at its Puducherry facility that included uncontrolled shreddin... Read More
A warning letter was issued by the U.S. FDA to Foshan Jinxiong Technology, a contract manufacturer of over-the-counter drugs for children, citing four violations related to quality control. After the inception last Augus... Read More
For violation of current good manufacturing practice norms, including failure to investigate the presence of a carcinogen in a solvent USFDA has pulled up Lantech Pharmaceuticals at its Andhra Pradesh-based manufacturing... Read More
US public health officials warned who aren’t already smokers to avoid e-cigarettes and other vaping devices after a mysterious outbreak of a serious lung disease which has sickened 215 individuals across 25 states... Read More
AbbVie’s new treatment for rheumatoid arthritis was approved by the U.S. Food and Drug Administration. It is a win for the drug maker seeking to widen its portfolio as its blockbuster flagship therapy Humira faces comp... Read More
A complete response letter (CRL) was issued by the US Food and Drug Administration (US FDA) for the New Drug Application (NDA) for insulin glargine filed by partner Mylan, said Biocon. In response to the observations mad... Read More
© Copyright 2023 Compliance Trainings. All Rights Reserved. Design & Developed by Eclick Softwares & Solutions Pvt. Ltd..
