Årsredovisning Med Information Från Form 20-F 2008 Inledning 2
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(R&D) Tax Credit
Report toThe the Pennsylvania Pennsylvania Department of General Revenue Assembly Bureau of Research on the Research and Development (R&D) Tax Credit The Pennsylvania Department of Revenue Bureau of Research March 15, 2012 Pennsylvania Research and Development Tax Credit Page 1 of 14 The Pennsylvania R&D Tax Credit Statute On May 7, 1997, Act 7 of 1997 created the Pennsylvania research and development (R&D) tax credit. The R&D tax credit provision became Article XVII-B of the Tax Reform Code of 1971 (TRC). The intent of the R&D tax credit was to encourage taxpayers to increase R&D expenditures within the Commonwealth in order to enhance economic growth. The terms and concepts used in the calculation of the Commonwealth’s R&D tax credit are based on the federal government’s R&D tax credit definitions for qualified research expense.1 For R&D tax credits awarded between December 1997 and December 2003, Act 7 of 1997 authorized the Department of Revenue (Department) to approve up to $15 million in total tax credits per fiscal year. Additionally, $3 million of the $15 million was set aside for “small” businesses, where a “small business” is defined as a “for-profit corporation, limited liability company, partnership or proprietorship with net book value of assets totaling…less than five million dollars ($5,000,000).” Over the years, several changes have been made to the R&D tax credit statute. Table 1 lists all of the acts that have changed the R&D tax credit statute, along with the applicable award years, the overall tax credit cap and the “small” business set aside. -
February 19, 2014
CANCER PREVENTION AND RESEARCH INSTITUTE OF TEXAS Oversight Committee Meeting February 19, 2014 CANCER PREVENTION AND RESEARCH INSTITUTE OF TEXAS Summary Overview of the February 19, 2014, Oversight Committee Meeting Please find enclosed the meeting packet for the next meeting of the CPRIT Oversight Committee to be held on Wednesday, February 19, 2014, at 10:00 AM. This summary overview of major agenda items provides background on key issues for Committee consideration. CEO Report Wayne Roberts will present the CEO’s report and address issues assigned by the Oversight Committee at the January 24th meeting including reconstituting the University Advisory Committee (UAC) and proposed dashboard metrics for the agency. Chief Scientific Officer Program Portfolio Presentation and Grant Award Recommendations Dr. Margaret Kripke will present the Program Integration Committee’s recommendations for scientific research awards. The research continuation grant recommendations are the first grant applications to be considered under the “new” review process set out by SB 149. SB 149 changed the way that grant recommendations are formally approved. A vote by two-thirds of the Oversight Committee that are present and voting (i.e. not recused because of a conflict of interest) is required to approve each funding recommendation. If two-thirds of the Oversight Committee does not vote to approve an award recommendation, then a statement explaining the reason for not following the PIC’s recommendation must be included in the meeting minutes. Product Development Officer Program Portfolio Presentation and Grant Award Recommendations Kristen Doyle, acting Product Development Officer, and Dr. Jack Geltosky, CPRIT’s Product Development Review Council Chair, will discuss CPRIT’s product development portfolio and present the Chief Executive Officer’s recommendations for product development grant awards. -
Drug Repositioning: Extracting Added Value from Prior R&D Investments
Drug Repositioning: Extracting Added Value from Prior R&D Investments Hermann A.M. Mucke, Ph.D. InsightPharmaReports.com Drug Repositioning: Extracting Added Value from Prior R&D Investments Hermann A.M. Mucke, Ph.D. Published in July 2010 by Cambridge Healthtech Institute • www.InsightPharmaReports.com • Reproduction prohibited i Insight Pharma Reports is a division of Cambridge Healthtech Institute, a world leader in life science information and analysis through conferences, research reports, and targeted publications. Insight Pharma Reports focus on pharmaceutical R&D—the technologies, the companies, the markets, and the strategic business impacts. They regularly feature interviews with key opinion leaders; surveys of the activities, views, and plans of individuals in industry and nonprofit research; and substantive assessments of technologies and markets. Managers at the top 50 pharma companies, the top 100 biopharma companies, and the top 50 vendors of tools and services rely on Insight Pharma Reports as a trusted source of balanced and timely information. Related Report Data Mining in Drug Development and Translational Medicine by Hermann A.M. Mucke, Ph.D. General Manager: Alfred R. Doig, Jr. 781-972-1348, [email protected] Editorial Operations Director: Laurie Sullivan 781-972-1353, [email protected] Design Director: Tom Norton 781-972-5440, [email protected] Production Director: Ann Handy 781-972-5493, [email protected] Marketing Manager: James Prudhomme 781-972-5486, [email protected] Customer Service: Rose LaRaia 781-972-5444, [email protected] Corporate Subscriptions: David Cunningham 781-972-5472, [email protected] Global Report Sales: Jack Valeri 781-972-1355, [email protected] Insight Pharma Reports, 250 First Ave., Suite 300, Needham, MA 02494 www.InsightPharmaReports.com ii • www.InsightPharmaReports.com • Reproduction prohibited Drug Repositioning: Extracting Added Value from Prior R&D Investments Hermann A.M. -
(R&D) Tax Credit
Report to theThe Pennsylvania Pennsylvania Department General of Revenue Assembly Bureau of Research on the Research and Development (R&D) Tax Credit The Pennsylvania Department of Revenue Bureau of Research March 15, 2010 Pennsylvania Research and Development Tax Credit Page 1 of 15 The Pennsylvania R&D Tax Credit Statute As part of the Fiscal Year 2009-10 budget, Act 48 of 2009 reduced the amount of tax credits available under several tax credit programs that can be awarded during the following two years. Act 48 reduced the total amount of R&D tax credit available in FY 2009-10 from $40 million to $20 million and in FY 2010-11 from $40 million to $18 million. Starting in FY 2011-12, the total amount of R&D tax credit the Department can award returns to $40 million per year. ******** On May 7, 1997, Act 7 of 1997 created the Pennsylvania research and development (R&D) tax credit. The R&D tax credit provision became Article XVII-B of the Tax Reform Code of 1971 (TRC). The intent of the R&D tax credit was to encourage taxpayers to increase R&D expenditures within the Commonwealth in order to enhance economic growth. The terms and concepts used in the calculation of the Commonwealth’s R&D tax credit are based on the federal government’s R&D tax credit definitions for qualified research expense.1 Over the years, several changes have been made to the R&D tax credit statute. On December 23, 2003, Governor Edward G. Rendell signed Act 46 of 2003 into law. -
יומן הפטנטים והמדגמים Patents and Designs Journal
י /' התשס"ח 5/2008 רשומות ISRAEL STATE RECORDS ו' באב התשס"ח August 7, 2008 יומן הפטנטים והמדגמים PATENTS AND DESIGNS JOURNAL פטנטים עמוד PATENTS Page בקשות שהוגשו Applications filed 1507 בקשות שקובלו Applications accepted 1775 פטנטים שניתנו Patents granted 1992 פטנטים שחודשו Patents renewed 1993 פטנטים שתוקפם פקעו Patents not in force 1995 פטנטים שחודשו לעשרים שנה Patents renewed for 20 years 1996 פטנטים שפג תוקפם Patents expired 1997 הודעות Notices 1998 שינויים בפרטים רשומים Changes in particulars entered בפנקס in register 2001 תיקוני טעויות Corrigenda 2002 מפתחות לבקשות שקובלו Indices of applications accepted i מדגמים DESIGNS מדגמים שנרשמו Designs registered 2004 מדגמים שחודשו Designs renewed 2017 מדגמים שבוטלו Designs void 2018 ו' באב התשס"ח – August 7, 2008 1507 ידיעות כלליות מכתבים, מסמכים, וכו' בענייני פטנטים ומדגמים יש לשלוח אל: רשם הפטנטים והמדגמים, רח' הסדנא 4, ירושלים לשכת הפטנטים נמצאת ברח' הסדנא 4, תלפיות, ירושלים והיא פתוחה לציבור בימי חול שאינם ערבי שבת או מועד בין השעות 8:30 ו - 12:30. לשכת הפטנטים מספקת תצלומים של פירוטים ושרטוטים במחיר של 2.50 שקלים בעד כל עמוד או חלק ממנו. אגרות ללשכת הפטנטים מתקבלות אך ורק על ידי תשלום לחשבון הלשכה בבנק הדואר מס' 0-24145-2. יש להציג קבלת בנק הדואר ללשכה יחד עם הבקשה לפעולה שעבורה האגרה שולמה. GENERAL INFORMATION Letters, documents, etc. concerning Patents and Designs should be addressed to: The Commissioner of Patents and Designs, 4 Hasadnah St., Jerusalem The Patent Office is located at 4 Hasadnah St., Talpiot, Jerusalem and is open to the public on weekdays, except on Fridays or on the eves of holydays, from 08:30 to 12:30 hrs. -
1999 Annual Report and Form 20-F CONTENTS
1999 Annual Report and Form 20-F CONTENTS Key Achievements in 1999 1 Financial Highlights 2 Shareholder Highlights 5 Chairman’s Statement 6 Chief Executive’s Review 7 Operational Review 8 Safety, Health and Environment 32 In April 1999, Astra AB and Zeneca Group PLC People and Community 34 merged to form AstraZeneca, one of the world’s Financial Review 35 leading pharmaceutical and agrochemical Board of Directors and Officers companies, which provides innovative, effective of the Company 48 products to improve health, nutrition and quality Directors’ Report 49 of life worldwide. The company is research and Financial Statements 55 technology intensive, with extensive international Financial statements and notes development and marketing skills. Its healthcare relating to the financial statements 55 business is strategically focused on seven major Principal subsidiaries, joint ventures therapeutic areas: gastrointestinal, oncology, pain and associates 118 control and anaesthesia, cardiovascular, central Additional information for US investors 120 nervous system, respiratory and infection. Zeneca Group Financial Record 129 Agrochemicals provides crop protection products Shareholder Information 131 designed to improve crop yields and food quality. Exchange rates 138 Definitions 139 Glossary of Terms 140 Cross Reference to Form 20-F IBC Cautionary statement regarding forward-looking statements In order to utilise the ‘Safe Harbor’ provisions of the United States Private Securities Litigation Reform Act of 1995, AstraZeneca is providing the following cautionary statement. This Annual Report and Form 20-F 1999 contains forward-looking statements with respect to the financial condition, results of operations and businesses of AstraZeneca. By their nature, forward-looking statements and forecasts involve risk and uncertainty because they relate to events and depend on circumstances that will occur in the future. -
Astrazeneca Annual Report 2006
AND FORM 20-F ANNUAL INFORMATION REPORT 2006 CONTENTS 2006 IN BRIEF 1 FINANCIAL STATEMENTS 19. Reserves 120 CHAIRMAN’S STATEMENT 2 Preparation of the Financial Statements 20. Minority interests 121 CHIEF EXECUTIVE OFFICER’S REVIEW 3 and Directors’ Responsibilities 96 21. Dividends to shareholders 121 FINANCIAL HIGHLIGHTS 6 Directors’ Responsibilities for, and Report 22. Acquisitions of on, Internal Control over Financial DIRECTORS’ REPORT business operations 121 Reporting 96 Business review 8 23. Disposal of business operations 123 Auditors’ Reports on the Financial 24. Post-retirement benefi ts 123 > Business environment 9 Statements and on Internal Control over > Strategy 11 Financial Reporting (Sarbanes-Oxley Act 25. Employee costs and share option plans for employees 128 > Our resources, skills Section 404) 97 and capabilities 12 Independent Auditors’ Report to the 26. Commitments and contingent liabilities 133 > Measuring performance 15 Members of AstraZeneca PLC (Group) 97 27. Leases 146 > Therapy area review Consolidated Income Statement 98 28. Statutory and other information 146 – Cardiovascular medicines 16 Consolidated Statement of Recognised Income and Expense 98 29. Share capital of parent – Gastrointestinal medicines 20 Consolidated Balance Sheet 99 company 147 – Neuroscience medicines 23 Consolidated Cash Flow Statement 100 Principal Subsidiaries 148 – Oncology medicines 26 Accounting Policies (Group) 101 Additional Information for US Investors 149 – Respiratory and Independent Auditors’ Infl ammation medicines 29 Notes to the Financial Statements (Group) Report to the Members of – Infection medicines 32 AstraZeneca PLC (Company) 157 1. Operating profi t 104 > Geographic review 33 Company Balance Sheet 158 2. Profi t on sale of interest > Research and development 37 in joint venture 104 Accounting Policies (Company) 159 > Development pipeline table 40 3. -
Zusammenfassung Dit-Votum Vom 01.01.2005 Bis 31.12.2005
Zusammenfassung dit-Votum vom 01.01.2005 bis 31.12.2005 ISIN Gesellschaft Antrag- Mgmt- dit- Datum-HV Tagesordnungspunkt steller Empfehlung Votum Art-HV ES0105200416 Abengoa S.A. 25.06.2005 AGM 1 Genehmigung von Einzel- und Konzernjahresabschluss für das Geschäftsjahr 2004; Mgmt für für Genehmigung der Entlastung der Directors 2 Genehmigung der Gewinnzuweisung Mgmt für für 3 Wahl der Abschlussprüfer für Unternehmen und konsolidierten Konzern Mgmt für für 4 Änderung von Artikel 39 bezüglich: Erhöhung der maximalen Anzahl an Mgmt für für Vorstandsmitgliedern von 7 auf 9 5 Wiederwahl, Nominierung und/oder Bestätigung von Mitgliedern des Vorstands Mgmt für für 6 Ermächtigung zur Ausgabe von Aktien oder aktiengebundenen Anleihen ohne Mgmt für gegen Bezugsrechte 7 Ermächtigung zur zusätzlichen Ausgabe von wandelbaren und nicht wandelbaren Mgmt für für Schuldverschreibungen und/oder Schuldpapieren 8 Genehmigung zum Rückkauf von Anteilen Mgmt für für 9 Genehmigung für Aufsichtsrat zur Ratifizierung und Umsetzung der genehmigten Mgmt für für Beschlüsse 10 Bestätigung des Versammlungsprotokolls Mgmt für für ES0105200416 Abengoa S.A. 15.10.2005 EGM 1 Vorlage des Aktienrückkaufplans; Ermächtigung des Aufsichtsrats zur Festlegung der Management Für Für Bedingungen für den Aktienrückkaufplan 2 Genehmigung zum Rückkauf von Anteilen Management Für Für 3 Genehmigung für den Aufsichtsrat zur Ratifizierung und Umsetzung der genehmigten Management Für Für Beschlüsse bezüglich: Aktienrückkauf 4 Bestätigung des Versammlungsprotokolls Management Für Für US00339B1070 Abgenix, Inc. 13.06.2005 AGM 1.1 Wahl von R. Scott Greer zum Director Mgmt für für 1.2 Wahl von M.K. Behrens, Ph.D., zum Director Mgmt für für 1.3 Wahl von R.S. Kucherlapati Ph.D., zum Director Mgmt für für 1.4 Wahl von Kenneth B. -
Collaborative Drug Discovery's 10 Anniversary Community Meeting
Collaborative Drug Discovery’s 10th Anniversary Community Meeting April 4th, 2014 8am-6pm UCSF Mission Bay Conference Center 1675 Owens St. San Francisco, CA 94158 Please use this Twitter hashtag for the event: #CDDx14 Agenda 7:45 Registration - refreshments in Foyer and Exhibition room 8:15 Opening Remarks - with UCSF Host, Stephanie Robertson and CDD CEO, Barry Bunin Collaborative Workflow: Basic and Advanced Use Cases of CDD Vault 8:20 Charlie Weatherall (CDD) & Anna Spektor (CDD) 9:10 Morning Sessions - moderated by Sylvia Ernst (CDD) The Rockefeller University Compound Screening Library 9:15 J. Fraser Glickman (Rockefeller University) Recent Progress in De-Orphanization of Nuclear Receptors 9:40 Ruo Steensma (Orphagen Pharmaceuticals) 10:05 Morning Break - located in the Foyer and Exhibition room Large small molecules in a Small large molecule world 10:35 Leanna Staben (Genentech) Linking the Molecular Structure of Medicines to their Biological Effects 11:00 Bob Volkmann (Systamedic & Mnemosyne Pharmaceuticals) Panel: Externalized Research - What Makes a Good Partnership? Wisdom from Experts 11:25 Who've "Been There - Done That," moderated by Sylvia Ernst (CDD) 11:50 Lunch - boxed lunches in the Foyer and Exhibition room Optional: “What if CDD had...” provide feedback to our product team (12:35) Kellan Gregory (CDD) 10 Years Evolving Our Collaborative Drug Discovery Vaults 1:05 Barry Bunin (CDD) CDD Vault: Noteworthy recent enhancements and a preview of things to come 1:30 David Blondeau (CDD) & Kellan Gregory (CDD) 2:20 Afternoon sessions - moderated Christopher Lipinski The Tuberculosis Drug Accelerator: A New Paradigm For Drug Discovery 2:25 Jerry Shipps (Tuberculosis Drug Accelerator) The role of NIAID in the development of therapeutics for Infectious Diseases 2:50 Martin John Rogers (NIAID) 3:15 Afternoon Break - located in the Foyer and Exhibition Room Targeting the Immunoproteasome 3:40 Dustin L. -
30388 OID RS Annual Review
Review of the Year 2005/06 >> President’s foreword In the period covered by this review*, the Royal Society has continued and extended its activities over a wide front. There has, in particular, been an expansion in our international contacts and our engagement with global scientific issues. The joint statements on climate change and science in Africa, published in June 2005 by the science academies of the G8 nations, made a significant impact on the discussion before and at the Gleneagles summit. Following the success of these unprecedented statements, both of which were initiated by the Society, representatives of the science academies met at our premises in September 2005 to discuss how they might provide further independent advice to the governments of the G8. A key outcome of the meeting was an We have devoted increasing effort to nurturing agreement to prepare joint statements on the development of science academies overseas, energy security and infectious diseases ahead particularly in sub-Saharan Africa, and are of the St Petersburg summit in July 2006. building initiatives with academies in African The production of these statements, led by the countries through the Network of African Russian science academy, was a further Science Academies (NASAC). This is indicative illustration of the value of science academies of the long-term commitment we have made to working together to tackle issues of help African nations build their capacity in international importance. science, technology, engineering and medicine, particularly in universities and colleges. In 2004, the Society published, jointly with the Royal Academy of Engineering, a widely Much of the progress we have has made in acclaimed report on the potential health, recent years on the international stage has been environmental and social impacts of achieved through the tireless work of Professor nanotechnologies. -
Annual Report and Form 20-F Information 2003 AZ AR Innercovs.Qxd 18/2/04 3:58 PM Page 1
AZ_AR_OuterCovs.qxd 18/2/04 3:59 PM Page 1 AstraZeneca Annual Report and Form 20-F Information 2003 Annual Report and Form 20-F Information 2003 AZ_AR_InnerCovs.qxd 18/2/04 3:58 PM Page 1 AstraZeneca Annual Report and Contents Form 20-F Information 2003 Contents Cross Reference to The information in this document that is r Key Achievements 01 Financial Statements 21. Reserves 86 with the Securities and Exchange Comm Chairman’s Statement 02 Preparation of the Financial Statements 22. Net cash inflow from into any filings by AstraZeneca under the Global Market Overview 03 and Directors’ Responsibilities 60 trading operations 87 such major headings, including subhead Chief Executive’s Review 04 Basis of Consolidation and Presentation 23. Cash flows related Graphs are not included unless specifica Financial Highlights 05 of Financial Information 60 to exceptional items 87 SEC passed comment upon the accurac Board of Directors 06 Independent Auditor’s Report to the 24. Acquisitions of subsidiaries and information and may be updated from tim Members of AstraZeneca PLC 61 purchases of minority interests 87 Strategy 08 Group Profit and Loss Account 62 25. Disposals of business operations 88 Operational Review 09 Group Statement of Total Recognised 26. Reconciliation of net cash flow Cardiovascular 10 Item Gains and Losses 62 to movement in net funds 88 3 Key Information Gastrointestinal 12 Group Balance Sheet 64 27. Analysis of net funds 89 Neuroscience 14 A. Selected financial data Statement of Group Cash Flow 65 28. Financing 89 Financial Highlights Oncology 16 Accounting Policies 66 29. Post-retirement benefits 90 Group Financial Record Respiratory and Inflammation 18 Notes to the Financial Statements 30. -
En Innehållsanalys Av VD-Ordet I Kontrast Till Årsredovisningens Övriga Delar
GÖTEBORGS UNIVERSITET HANDELSHÖGSKOLAN Företagsekonomi - Externredovisning Företagsekonomiska institutionen En innehållsanalys av VD-ordet i kontrast till årsredovisningens övriga delar Magisteruppsats i redovisning Hösten 2008 Handledare: PhD Inga-Lill Johansson Författare: Achim Lang Kristofer Weiler Anna-Maria Wiaderny Förord Vi vill först och främst tacka vår handledare Inga-Lill Johansson som på ett föredömligt sätt gjort sig anträffbar, tagit sig tid och bidragit med värdefulla insikter. Varje handledningsmöte har hos oss främjat en djupare analys, nytänkande kreativitet men också utmaning, vilket fört vårt arbete framåt, men även fungerat som en sporre för uppsatsens hela kvalitet. Vi vill också tacka våra familjer som haft förståelse och tålamod under denna intensiva tid. Göteborg den 9 januari 2009 ___________________ ___________________ ___________________ Achim Lang Kristofer Weiler Anna-Maria Wiaderny i Abstract Thesis title: A content analysis of the CEO-letter in contrast with the financial statements of the annual report. Keywords: Annual report, CEO-letter, accounting, communication Authors: Achim Lang, Kristofer Weiler & Anna-Maria Wiaderny Advisor: PhD Inga-Lill Johansson Problem description: The users of the annual report demand correct information to make adequate investment decisions. The annual report is composed of one regulated part by International Financial Reporting Standard - IFRS, as well as a voluntary part, the CEO-letter, that is not regulated. Today the CEO-letter has obtained more importance because it is easier to comprehend for those who do not attain knowledge of accounting. A problem arises of how the CEO chooses to image the economical reality, as it is presented in the accounting, or if he chooses to distort the reality in the CEO-letter.