Search for: "MASTERS DRUG COMPANY"
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1 Dec 2016, 6:52 am
The Court then cited Master Financial, Inc. v. [read post]
8 Jan 2017, 10:00 pm
Three warning letters recently posted by the Food and Drug Administration cited food safety violations at a tofu production plant in California, a supplement company in Nebraska and a supplier of fish roe based in Peru. [read post]
3 Oct 2007, 9:55 pm
According to ACI, this is the "one and only event that has consistently allowed brand name and generic drug makers to benchmark their companies' current strategies and tactics against competitors in both camps. [read post]
25 Sep 2008, 10:47 am
Post 1970 Indian generic companies including Cipla made phenomenal growth (in absence of patent protection for pharmaceutical drug products) to thousand crore plus company but still Indian healthcare scenario is struggling for better infrastructure. [read post]
1 Jan 2018, 9:59 pm
Based on our review, we have concluded that your BrainAlert product is an unapproved new drug and misbranded drug and that, even if it were not a drug, it would be a misbranded dietary supplement. [read post]
28 Jan 2022, 2:01 pm
In September 2015, the Food and Drug Administration (“FDA”) placed an order (one base year plus four option years) under Carahsoft’s Schedule Contract for a subscription to Avue’s software platform. [read post]
31 Aug 2014, 10:03 pm
Food and Drug Administration recently published warning letters issued to a dairy farm, a seafood company and two dietary supplement makers. [read post]
18 May 2007, 7:51 am
(The most prominent example, obviously, is the tobacco Master Settlement Agreement.) [read post]
25 Apr 2012, 4:30 am
The Sixth Circuit observed that the plaintiff is master of his complaint and can plead to avoid federal jurisdiction. [read post]
24 Nov 2009, 3:30 pm
Connie Barton and Donna Kendall both have something in common: they stood up to one of the largest and most powerful drug companies in court - and won. [read post]
22 Dec 2011, 1:15 pm
Accutane side effects and injuries have prompted 6,634 people to file an Accutane lawsuit in New Jersey against the manufacturer of the controversial acne drug, Hoffman-LaRoche. [read post]
12 Feb 2016, 7:30 pm
They should return it to the point of purchase,” according to the company’s recall notice on the Food and Drug Administration’s website. [read post]
4 Jun 2012, 6:19 am
“Here you have ICE making a seizure, based on the say-so of the record company guys, and getting secret extensions as they wait for their masters, the record companies, for evidence to prosecute,” Cohn said in a telephone interview. [read post]
11 Sep 2009, 8:51 pm
According to ACI, this is "the one and only event that consistently allows brand name and generic drug makers to benchmark their companies' current strategies and tactics against competitors in both camps. [read post]
7 May 2018, 9:01 pm
The lawsuit, referred to as a master consolidated complaint, consolidates four similar actions filed in February and March against the company. [read post]
17 Nov 2009, 6:00 am
The pharmaceutical company was able to use these data in conjunction with its own manufacturing, labeling, and other information to complete the new animal drug application. [read post]
8 Jul 2014, 10:02 pm
FDA also noted that the company’s response in December was inadequate because no written master manufacturing record was prepared and followed for each “unique formulation of a dietary supplement,” specifically Elderberry Concentrate Dietary Supplement products. [read post]
9 Jun 2011, 2:59 am
At 985 locations around the United States, companies hold medicated feed licenses from the U.S. [read post]
7 Jun 2020, 9:01 pm
As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its jurisdiction. [read post]
22 Nov 2020, 9:01 pm
As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its jurisdiction. [read post]
