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15 May 2012, 9:19 am
Malpractice defense lawyers learned this trick at the feet of the master: pharmaceutical companies make a concerted effort to use its influence at major universities to blackball anyone who testifies against them. [read post]
3 Jul 2011, 9:59 pm
ACI faculty will help attendees: • Master the basics of the application and approval processes for drugs, biologics, and devices; • Comprehend the structure of the FDA and the roles of the three major agency centers: CDER, CBER, and CDHR; • Develop a practical working knowledge of clinical trials for drugs and biologics and the clearance process for devices; • Learn how devices are classified, monitored, and regulated; • Appreciate the complexities of pharmaceutical… [read post]
13 Jan 2012, 9:04 pm
ACI faculty will help attendees: • Master the basics of the application and approval processes for drugs, biologics, and devices; • Comprehend the structure of the FDA and the roles of the three major agency centers: CDER, CBER, and CDHR; • Develop a practical working knowledge of clinical trials for drugs and biologics and the clearance process for devices; • Learn how devices are classified, monitored, and regulated; • Appreciate the complexities of pharmaceutical… [read post]
14 Feb 2012, 6:45 am
It certainly shows how financial lawyers may need to master some of the intricacies of participating in administrative rulemaking. [read post]
19 Oct 2011, 2:07 pm
According to a news report in The Orange County Register, the injury pedestrian collision occurred on Laguna Canyon Road near the Festival of Arts/Pageant of the Masters. [read post]
13 Jan 2012, 9:04 pm
ACI faculty will help attendees: • Master the basics of the application and approval processes for drugs, biologics, and devices; • Comprehend the structure of the FDA and the roles of the three major agency centers: CDER, CBER, and CDHR; • Develop a practical working knowledge of clinical trials for drugs and biologics and the clearance process for devices; • Learn how devices are classified, monitored, and regulated; • Appreciate the complexities of pharmaceutical… [read post]
27 Apr 2009, 8:26 am
” But we need those Masters of The Universe, Krugman! [read post]
16 Dec 2011, 9:12 pm
C5 faculty will help attendees: • Overcome the regulatory hurdles blocking biosimilar approval by increasing knowledge of EMA guidelines; • Discover how the development of the FDA regulatory approval pathway will affect market access for biosimilars in the United States; • Hear legal advice on information exchange between applicants and patent holders to establish a framework for clinical development of a biosimilar; • Refine patent protection strategy by mastering the… [read post]
15 May 2012, 9:19 am
Malpractice defense lawyers learned this trick at the feet of the master: pharmaceutical companies make a concerted effort to use its influence at major universities to blackball anyone who testifies against them. [read post]
25 Jun 2010, 9:26 pm
ACI faculty will help attendees: • Master the complexities of pharmaceutical iP and the regulatory balance between brand name and generic products; • Analyze the future of follow-on biologics following recent health care reform legislation; • Recognize the pivotal role of labeling in the drug and biologics approval process; • Comprehend the structure of the FDA and the roles of the three major agency centers: CDER, CBER, and CDHR; • Understand the basics of the… [read post]
21 Jan 2011, 10:05 pm
ACI faculty will help attendees: • Master the basics of the application and approval processes for drugs, biologics, and devices; • Comprehend the structure of the FDA and the roles of the three major agency centers: CDER, CBER, and CDHR; • Develop a practical working knowledge of clinical trials for drugs and biologics and the clearance process for devices; • Learn how devices are classified, monitored, and regulated; • Appreciate the complexities of pharmaceutical… [read post]
13 Jul 2007, 5:55 pm
DPA spokeswoman Lynelle Jolley said Judge Gail Ohanesian rejected an initial request by the union representing 3,500 state attorneys and hearing officers to appoint a special master to study just how lousy their pay is compared with what their colleagues in other public agencies earn. [read post]
28 Feb 2008, 11:02 am
On his Legal Pad blog, Roger Parloff is reporting that, on Wednesday, a special master in the federal shareholders class-action against Coke recommended that Coughlin Stoia, which has worked on the case for seven years, be barred from serving as class counsel because it allegedly purchased â [read post]
16 Sep 2011, 9:32 pm
The conference will allow attendees to: • Pinpoint patents that may be vulnerable to a Paragraph IV challenge; • Demystify an ANDA applicant's Orange Book strategy and dissecting a challenger's obligations under Paragraph IV; • Understand the FTC's current position on pay-for-delay settlements and anticipating any antitrust concerns stemming from agreements between brand names and generics; • Master the intricacies of litigation with multiple ANDA filers;… [read post]
13 Jul 2012, 8:06 pm
ACI faculty will help attendees: • Master the basics of the application and approval processes for drugs, biologics, and devices; • Comprehend the structure of the FDA and the roles of the three major agency centers: CDER, CBER, and CDHR; • Develop a practical working knowledge of clinical trials for drugs and biologics and the clearance process for devices; • Learn how devices are classified, monitored, and regulated; • Appreciate the complexities of pharmaceutical… [read post]
27 Jan 2014, 8:17 am
In this edition of The Digital Edge - Lawyers and Technology podcast, Time Management for Lawyers, Sharon Nelson and Jim Calloway invite Dixon to discuss her top tips for legal professionals looking to master project management, how to stop procrastinating, and more (I really hate it when I forget to blog about something really great like this when it is posted. [read post]
22 Jan 2010, 9:59 pm
ACI faculty will help attendees: • Master the basics of the application and approval processes for drugs, biologics, and devices; • Comprehend the structure of the FDA and the roles of the three major agency centers: CDER, CBER, and CDHR; • Develop a practical working knowledge of clinical trials for drugs and biologics and the clearance process for devices; • Learn how devices are classified, monitored, and regulated; • Appreciate the complexities of pharmaceutical… [read post]
23 Jul 2010, 9:42 pm
ACI faculty will help attendees: • Master the complexities of pharmaceutical iP and the regulatory balance between brand name and generic products; • Analyze the future of follow-on biologics following recent health care reform legislation; • Recognize the pivotal role of labeling in the drug and biologics approval process; • Comprehend the structure of the FDA and the roles of the three major agency centers: CDER, CBER, and CDHR; • Understand the basics of the… [read post]
8 Nov 2006, 10:59 am
But there are many more functions that you [and I] never use and never take time to explore.These BNET downloads will help you master new Word skills with a focus on using tables. [read post]
4 Oct 2008, 9:35 pm
IN NEW YORK, A PREFAB INSTANT SUBURB: Tourists press up against the construction fence on the corner of 53rd and Sixth, staring speechless as a giant crane lifts an entire bathroom into the air and deposits it in what will be a master bedroom. [read post]
