Eli Lilly Company

The Batch Reaction Subcommittee was chaired by Walter L. Lrank of EQE International. Current members of the subcommittee, listed alphabetically are David J. Christensen, Union Carbide Corporation Warren Greenfield, International Specialty Products Philip P. Malkewicz, Nalco Chemical Company Peter L. McGrath, Olin Corporation Louisa A. Nara, Bayer Corporation Leslie A. Seller, CCPS Staff Consultant Robert Schisla, Eastman Chemical Company Anthony Torres, Eastman Kodak Company Dr. Jan C. Windhorst, Nova Chemicals and Paul Wood, Eli Lilly Company. Eormer subcommittee members who contributed much in getting this project started were Eelix Ereiheiter, CCPS Staff Consultant (deceased) A1 Noren, Monsanto Company-Searle (deceased) John Noronha, Eastman Kodak Company (retired) and Robert Stankovich, Eli Lilly Company. 

It is a pleasure to acknowledge the skillful and dedicated efforts of our co-workers whose names are to be found among the references and whose achievements have provided the basis of this review. We are also grateful to N.A.T.O. for the provision of Research Grant Number 1559 which has enabled us to collaborate in the production of this article. Our work has been supported by the National Institutes of Health, the National Science Foundation, the Petroleum Research Fund, the Guggenheim Foundation, the Sloan Foundation, Research Corporation, Western Fher Company, Eli Lilly Company, and University of Puerto Rico (WA), and by the Science Research Council (AJB). 

D. Scott Coffey, Scott A. May and Andrew M. Ratz, Eli Lilly Company,... 

It should be remembered that this conversion is only approximate. Several other approximations have been used on the labels of certain tablets. For example. Saccharin tablets from Eli Lilly Company shows V2 gr (32 mg) on its label whereas the phenobarbital tablets from the same company have 30 mg (Z2 gr) on its label. Similarly sodium bicarbonate tablets from Eli Lilly have 5 grs (325 mg) on its label and potassium iodide from the same company has 300 mg (5 grs) on its container label. In the present book, it is advised to use one grain equivalent as 65 mg. 

If a physician prescribes 1V2 grains of phenobarbital sodium from the Eli Lilly Company, how many grams of drug would it contain ... 

Cymbalta (package insert). Indianapolis, IN, Eli Lilly Company, 2005... 

Eli Lilly Company Lilly Corporate Center Indianapolis IN 46025 USA... 

Marie Prewett Imclone Systems, a wholly-owned subsidiary of Eli Lilly Company, New York, NT, USA... 

Alsante et al. (262) recently reported the results a survey of American pharmaceutical companies, sponsored by Eli Lilly Company and Pfizer Inc., U.S. 

Humulin products (Eli Lilly Company) contain recombinant human insulin derived from Escherichia coli Novolin products (Novo Nordisk) are recombinant human insulin derived from Saccharomyces cerevisiae both companies also sell other forms of recombinant human insulin and may have additional forms (formulations or new drugs) in clinical trials. 

The current ISPOR 2000-2001 Board of Directors is as follows President Jon C. Clouse, M.Ph., M.S., Ingenix Pharmaceutical Services President-Elect Eva Lydick Ph.D., SmithKIinc Beccham Past President Bryan R. Luce Ph.D., M.B.A, MEDTAP International Directors A. Mark Fcndrick M.D., University of Michigan Medical Center Karen Rascati R.Ph., Ph.D., University of Texas Joan Rovira Ph.D., University of Barcelona and SOIKOS Kent H. Summers Ph.D., Eli Lilly Company Adrian Towse M.S., Mphil, Office of Health Economics (United Kingdom) and Executive Director Marilyn Dix Smith R.Ph., Ph.D. 

Reid Y, Storts D, Riss T, Minor L (2004-2013). Authentication of hitman cell lines by STR DNA profiling analysis. In Sittampalam GS, Gal-Edd N, Arkin M et al (eds) Assay guidance manual [Internet], Eli Lilly Company and the National Center for Advancing Translational Sciences, Bethesda, MD. Available http //www.ncbi.nlm.nih.gov/ books/NBKl44066/... 

Following the hearings, in 1972 GAO approached the Pharmaceutical Manufacturers Association (PMA) about doing a comprehensive study on the industry, including production process, efficiency, costs, and profits. PMA-member companies rejected GAO s request because the confidentiality of their cost and other data could not be protected.8 GAO revised its plan and proposed a Phase I study that would examine the characteristics and methods of the industry. Six companies voluntarily cooperated with this initial phase SmithKline Corporation, Bristol Laboratories, division of Bristol-Myers Company, Abbott Laboratories, Eli Lilly Company, Merck Company, Inc., and Hoffman La Roche. 

Executive Vice President Eli Lilly Company Indianapolis, IN... 

This chapter deals with the assessment of definitive and relative quantitative assays. A good reference on the analytical validation of a quasi-quantitative assay is a white paper on immunogenicity by Mire-Sluis et al. [6] and the guidance on assay development and validation for high-throughput screening developed by scientists from NIH and Eli Lilly Company [7]. 

Eli Lilly Company Chemical Product R D Lilly Development Centre S.A. 

Eli Lilly Company, Chemical Product R D, Lilly Development Centre S.A., Parc Scientifique de Louvain-la-neuve, Rue Granbonpre, 11, B-1348 Mont-Saint-Guibert, Belgium... 

---