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11 Mar 2014, 6:00 am
Master’s degree or higher may fall within the Master’s Cap; all others fall within the General Cap. [read post]
18 Mar 2014, 6:00 am
Master’s degree or higher may fall within the Master’s Cap; all others fall within the General Cap. [read post]
9 Jun 2011, 4:30 am
R. [read post]
4 Apr 2009, 9:25 am
My point is that Chandler seems to have mastered the art of subtle self-mockery, up to the edge of self-parody, at the start. [read post]
13 Jul 2010, 9:02 am
I asked my imediate supervisor what I should read to begin mastering the field. [read post]
7 Jun 2013, 10:31 am
Stan Chesley — the “Master of Disaster,” the “Prince of Torts” — is not going gently into that good night. [read post]
12 Jul 2013, 8:51 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 IP… [read post]
15 Sep 2014, 7:00 am
Yet, when up-and-coming attorneys master these straightforward tools, they will think and argue like the best lawyers. [read post]
1 Jan 2014, 11:36 am
The master was on board at the time, but evacuated safely. [read post]
18 Aug 2016, 11:12 am
It is no longer one of an onerous master, but rather one of a trusted advisor. [read post]
2 May 2014, 1:30 pm
Elmer Masters of CALI fame has written a blogpost on Slaw about Fargo the Outliner. [read post]
20 Sep 2013, 9:01 pm
Strafford will be offering a webinar/teleconference entitled "Strategic Use of Patent Reissue After the AIA -- Correcting Errors in Patents, Determining Whether and When to Pursue a Reissue Application, and Mastering the Recapture Rule" on October 31, 2013 from 1:00 to 2:30 pm (EDT). [read post]
9 May 2014, 8:01 am
Is a Master’s Degree worth the effort? [read post]
17 Jan 2014, 8:24 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]
12 Aug 2017, 8:13 pm
ACI faculty will help attendees: • Master the basics of the application and approval processes for drugs, biologics, and devices; • Comprehend the intricacies of expedited approval, combination products, and companion diagnostics; • Develop a practical working knowledge of clinical trials for drugs and biologics; • Learn about labeling and how it serves as the transition between the approval process and the post-approval world; • Appreciate the complexities of… [read post]
18 Jan 2013, 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]
7 Nov 2011, 9:47 pm
Master’s degree petitions has already been reached, and USCIS will continue to accept H-1B petitions for FY2012 until the cap of 65,000 is met. [read post]
19 Dec 2015, 9:50 pm
Strafford will be offering a webinar/teleconference entitled "Strategic Use of Patent Reissue: Determining Whether and When to Pursue a Reissue Application -- Correcting Errors, Responding to an IPR Challenge and Mastering the Recapture Rule" on January 14, 2016 from 1:00 to 2:30 pm (EST). [read post]
13 Feb 2015, 6:02 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]
30 Mar 2019, 8:45 pm
Bo An, Risk Management, Federal Reserve Bank of Chicago will moderate a panel consisting of Sarah Duda, Assistant General Counsel, Cboe Global Markets; Ted Tian, Master Agreements Negotiator, BP America, Inc.; Mark Fields, Partner, Alsop Louie Partners; and Matthew Kelly, Managing Director and Chief Intellectual Property Counsel, CME Group. [read post]
