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sponsors experience Abbott Eli Lilly Merck & Co. Sano-Aventis Aegerion Emergent Biosolutions Merz Pharmaceuticals Sano-Pasteur Allergen Exact Sciences Metabasis Therapeutics Sano-Synthelabo Alpharma Forbes Medi-Tech Nabi Pharmaceuticals Schering-Plough Altana Forest NanoBio Schwarz Pharmaceuticals Amgen Furiex Neuraxon Searle Amylin G&W Labs Neurogen Shionogi Arena Pharmaceuticals Galderma Novartis Solvay Astellas Genentech Novavax Stiefel Laboratories AstraZeneca Genomic Collaboration Noven Pharmaceuticals Surface Logix Aventis Gilead Novo Nordisk Takeda Barr GlaxoSmithKline Omthera Pharmaceuticals TAP Baxter Healthcare GlaxoSmithKline Biologicals Ortho McNeil Taro Pharmaceuticals Bayer Healthcare Glaxo Wellcome Pain Therapeutics Teva Pharmaceuticals Berlex Glenmark Pharmaceuticals Palatin Therapeutics Tioga Bertek Hoechst-Marion Roussel PaxVax TorreyPintes Therapeutics Bionovo Homan LaRoche Pharmacia Triangle Biovail IDEA AG Pharmos Corporation Trimel Biopharma Boehringer Ingelheim Impax Laboratories Pzer Tylenol Bristol-Myers Squibb Insmed Pozen UCB Centocor Jazz Pharmaceuticals Procter & Gamble Vanguard Cipher Johnson & Johnson ProEthic Vaxinnate Collagenex King Pharmaceuticals Promius Pharmaceuticals Viro Pharma Covidien KOS Pharmaceuticals QLT Warner Chilcott Daiichi Sankyo KOWA Pharmaceuticals Quinnova Pharmaceuticals Watson Pharmaceuticals DepoMed Lexicon Pharmaceuticals Rhone-Poulenc Rorer Wyeth Dow Marine Polymer Technologies Roche Wyeth Ayerst Dupont Merck Meade Johnson Roche Diagnostics Xenoport Duramed Medimmune R.W.T. XOMA LTD Dynport Vaccine Company Medivir Sankyo Yamanouchi If you would like more details about a potential clinical study opportunity with Coastal Carolina Research Center please contact: Nathan Morton Director of Business Development Phone #: 843-856-3784 Fax #: 843-856-3788 Email: [email protected] Study Experience Sponsors Experience CRO Experience.

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Appendix a 2016 Financial Report Financial Review Pfizer Inc
Appendix A 2016 Financial Report Financial Review Pfizer Inc. and Subsidiary Companies GLOSSARY OF DEFINED TERMS Unless the context requires otherwise, references to “Pfizer,” “the Company,” “we,” “us” or “our” in this 2016 Financial Report (defined below) refer to Pfizer Inc. and its subsidiaries. We also have used several other terms in this 2016 Financial Report, most of which are explained or defined below: 2016 Financial Report This Financial Report for the fiscal year ended December 31, 2016, which was filed as Exhibit 13 to the Annual Report on Form 10-K for the fiscal year ended December 31, 2016 2016 Form 10-K Annual Report on Form 10-K for the fiscal year ended December 31, 2016 AAV Adeno-Associated Virus ABO Accumulated postretirement benefit obligation ACA (Also referred to as U.S. U.S. Patient Protection and Affordable Care Act, as amended by the Health Care and Education Reconciliation Healthcare Legislation) Act. ACIP Advisory Committee on Immunization Practices ALK anaplastic lymphoma kinase Allergan Allergan plc Alliance revenues Revenues from alliance agreements under which we co-promote products discovered or developed by other companies or us AM-Pharma AM-Pharma B.V. Anacor Anacor Pharmaceuticals, Inc. Astellas Astellas Pharma U.S. Inc. ASU Accounting Standards Update ATM-AVI aztreonam-avibactam Bamboo Bamboo Therapeutics, Inc. Baxter Baxter International Inc. BMS Bristol-Myers Squibb Company CDC U.S. Centers for Disease Control and Prevention Cellectis Cellectis SA Celltrion Celltrion Inc. and Celltrion Healthcare,
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[Docket No. FDA-2017-N-3203] Wyeth Pharmaceutical
This document is scheduled to be published in the Federal Register on 06/21/2017 and available online at https://federalregister.gov/d/2017-12908, and on FDsys.gov 4164-01-P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA-2017-N-3203] Wyeth Pharmaceuticals Inc. et al.; Withdrawal of Approval of 121 New Drug Applications and 161 Abbreviated New Drug Applications AGENCY: Food and Drug Administration, HHS. ACTION: Notice. SUMMARY: The Food and Drug Administration (FDA) is withdrawing approval of 121 new drug applications (NDAs) and 161 abbreviated new drug applications (ANDAs) from multiple applicants. The holders of the applications notified the Agency in writing that the drug products were no longer marketed and requested that the approval of the applications be withdrawn. DATES: The withdrawal is effective on [INSERT DATE 30 DAYS AFTER DATE OF PUBLICATION IN THE FEDERAL REGISTER]. FOR FURTHER INFORMATION CONTACT: Florine P. Purdie, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 51, rm. 6248, Silver Spring, MD 20993-0002, 301-796-3601. SUPPLEMENTARY INFORMATION: The holders of the applications listed in table 1 in this document have informed FDA that these drug products are no longer marketed and have requested that FDA withdraw approval of the applications under the process in § 314.150(c) (21 CFR 314.150(c)). The applicants have also, by their requests, waived their opportunity for a hearing. Withdrawal of approval of an application or abbreviated application under § 314.150(c) is without prejudice to refiling. 2 Table 1 Application No.
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March 31, 2021
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1 United States District Court for the Southern District
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