Search for: "Ives, A. v. Ives, K." Results 141 - 160 of 625
Sorted by Relevance | Sort by Date
RSS Subscribe: 20 results | 100 results
28 Jun 2010, 11:31 am by robhealey
  SCHEDULE V examples include but are not limited to: Ephedrine, except as provided in division (K) of section 3719.44 of the Revised Code, and various other drugs in compound form. [read post]
1 May 2018, 4:14 am by Andrew Lavoott Bluestone
Sladkus, an attorney, brings this defamation action against Melanie Englese a/k/a Melanie Sisskind, his former client. [read post]
4 Mar 2013, 7:58 am
Happily Herr K was able to announce to his judicial inquisitor that someone manning security on the way into court had indeed addressed him as Mr Ka-link, to the general amusement of those in court -- both on the bench and before it. [read post]
1 Jan 2014, 5:01 pm by oliver randl
330 x 103 and a Mw/Mn of 20-35,and comprising(v) a low molecular weight (LMW) ethylene homopolymer fraction and a high molecular weight (HMW) ethylene copolymer fraction in a weight ratio of the LMW fraction to the HMW fraction of (35-55) : (65-45)(vi) said HMW ethylene copolymer fraction having a lower molecular weight limit of 3500.[2.2] The contested decision nor the parties on appeal addressed the question whether the present patent specification disclosed a technical concept fit for… [read post]
6 Sep 2012, 5:25 pm by FDABlog HPM
District Court for the District of Columbia dealt a blow to K-V Pharmaceutical Company’s (“KV’s”) efforts to “restore” orphan drug exclusivity for the pre-term birth drug MAKENA (hydroxyprogesterone caproate) Injection, 250 mg/mL, by granting FDA’s Motion to Dismiss a case filed by KV back in early July. [read post]
16 Dec 2024, 7:58 pm by Kurt R. Karst
  The guidance also clarifies the criteria for re-recognition of third party 510(k) review organizations and the suspension or withdrawal of recognition and discusses how FDA will audit the Third Party 510(k) Review Program as part of ongoing audit plans under the Quality Management and Organizational Excellence (QMOE) Program which are all Medical Device User Fee Amendments (MDUFA) IV and V commitments. [read post]
10 Apr 2017, 12:18 pm by Overhauser Law Offices, LLC
§ 1125(a) Count III: Unfair Competition Count IV: Trademark Dilution under 15 U.S.C. [read post]
5 Mar 2023, 9:01 pm by renholding
 The introductory language to Item 402(v) provides that PVP disclosure must be included in any “proxy or information statement” for which the SEC requires executive compensation disclosure pursuant to Item 402 of Regulation S-K. [read post]
9 Sep 2013, 9:23 am by Shamnad Basheer
He went on to defend his hypothesis based on text of Section 2(m) and 51(b)(iv). [read post]
9 Oct 2011, 5:01 pm by Oliver G. Randl
Claim 1 of all those requests, compared to claim 1 as granted, was restricted by the use of an additional ingredient (v) defined to be a single non-volatile emollient or a mixture of emollients selected from fatty acids, fatty alcohol esters, slightly water-soluble ethers and alcohols, hydrocarbons, water-insoluble ethers, mineral oils and polyorganosiloxanes. [read post]