Relevant bibliographies by topics / Pharmaceutical Excellence

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Pharmaceutical Excellence'

Author: Grafiati
Published: 2 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Pharmaceutical Excellence"

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Dupree, Lori H. "Achieving Excellence in Pharmaceutical Care." Southern Medical Journal 108, no. 10 (2015): 627. https://doi.org/10.14423/smj.0000000000000358.

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Hunter, Tracy S., Lisa Deziel-Evans, and Wallace A. Marsh. "Assuring Excellence in Distance Pharmaceutical Education." American Journal of Pharmaceutical Education 67, no. 3 (2003): 94. http://dx.doi.org/10.5688/aj670394.

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Hunter, Tracy S., Lisa Deziel-Evans, and Wallace A. Marsh. "Assuring Excellence in Distance Pharmaceutical Education." American Journal of Pharmaceutical Education 67, no. 3 (2003): 94. http://dx.doi.org/10.1016/s0002-9459(24)00682-x.

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Meyer, Susan M. "A Strategy to Examine Excellence in Pharmaceutical Education." American Journal of Pharmaceutical Education 67, no. 3 (2003): 86. http://dx.doi.org/10.5688/aj670386.

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Konnor, Delbert. "Advancing Pharmaceutical Care Through Vision, Leadership, and Excellence." Journal of Managed Pharmaceutical Care 1, no. 1 (2001): 7–17. http://dx.doi.org/10.1300/j234v01n01_03.

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Kinnell, Margaret. "Benchmarking for information service excellence: The pharmaceutical industry." Total Quality Management 8, no. 1 (1997): 3–14. http://dx.doi.org/10.1080/09544129710404.

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Volkin, David B., Susan Hershenson, Rodney J. Y. Ho, Susumu Uchiyama, Gerhard Winter, and John F. Carpenter. "Two Decades of Publishing Excellence in Pharmaceutical Biotechnology." Journal of Pharmaceutical Sciences 104, no. 2 (2015): 290–300. http://dx.doi.org/10.1002/jps.24285.

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Meyer, Susan M. "A Strategy to Examine Excellence in Pharmaceutical Education." American Journal of Pharmaceutical Education 67, no. 3 (2003): 86. http://dx.doi.org/10.1016/s0002-9459(24)00674-0.

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Jaffal, Shaima, and Khaled Alzou’bi. "Performance of the Supply Chain in Operational Excellence: A Field Study in Jordanian Pharmaceutical Companies." Business Series 3, no. 2 (2024): 201–51. http://dx.doi.org/10.59759/business.v3i2.593.

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This study aims to identify the role of supply chain performance dimensions (cost, flexibility, delivery, and responsiveness) in achieving operational excellence dimensions (leadership excellence, product excellence, employee excellence, organizational culture excellence, and strategic excellence) in Jordanian pharmaceutical companies. The study population includes all senior and middle managers (1016 employees) in (22) pharmaceutical companies in Amman. A stratified random proportional sample was used to represent the study population. The descriptive analytical approach was used to achieve t
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Sanjay Sarkhel. "Assessing the Impact of Operational Excellence and Employee Engagement on Performance in Pharmaceutical Industry." Journal of Information Systems Engineering and Management 10, no. 3 (2025): 71–105. https://doi.org/10.52783/jisem.v10i3.3744.

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The Indian pharmaceutical industry, a global player, faces challenges in balancing robust Human Resource Management (HRM) practices with operational excellence, which could hinder its growth and competitiveness. By addressing both HRM and operational excellence challenges, Indian pharmaceutical companies can create a more engaged workforce, optimize processes, and achieve sustainable growth in the competitive global market. With its significant economic expansion and worldwide funding, HRM in India has attracted substantial study focus throughout the last decade and remains to this day, althou
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Dissertations / Theses on the topic "Pharmaceutical Excellence"

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Coffey, Shonna (Shonna Marie). "Achieving business and operational excellence in the pharmaceutical industry." Thesis, Massachusetts Institute of Technology, 2008. http://hdl.handle.net/1721.1/43838.

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Thesis (M.B.A.)--Massachusetts Institute of Technology, Sloan School of Management; and, (S.M.)--Massachusetts Institute of Technology, Dept. of Chemical Engineering; in conjunction with the Leaders for Manufacturing Program at MIT, 2008.<br>Includes bibliographical references (p. 111-114).<br>Historically the pharmaceutical industry has been highly profitable. However, the increasing regulatory requirements, bargaining power of buyers, and drug failures together with the threat of biosimilars and decreasing R&D productivity are creating challenges for research driven pharmaceutical companies.
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Matheis, Sebastian. "Preparation of a Class A certification in the field of pharmaceutical packaging through mapping and optimization of business processes and implementation of the Oliver Wight Class A Behaviors for Business Excellence." Thesis, Uppsala universitet, Institutionen för biologisk grundutbildning, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-227771.

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On the road to success, companies need to fulfil their stakeholders’ expectations. On the road to business excellence, companies need to exceed these expectations. Oliver Wight Inc. has established a certification called Class A Business, which shows that a company is exceeding stakeholders’ expectations and that it performs in the upper quartile in its respective industry. The Class A Business certification is awarded, once a company fulfils a certification checklist with Class A Business criteria. To get to this point, a company can design their road to business excellence by following a spe
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Books on the topic "Pharmaceutical Excellence"

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Friedli, Thomas, Prabir Basu, Daniel Bellm, and Jürgen Werani, eds. Leading Pharmaceutical Operational Excellence. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-35161-7.

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Friedli, Thomas. Operational excellence in the pharmaceutical industry. Editio Cantor Verlag, 2006.

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Royal Pharmaceutical Society of Great Britain. Achieving excellence in pharmacy through clinical governance: Royal Pharmaceutical Society of Great Britain's policy on clinical governance. The Society, 2000.

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Friedli, Thomas, Prabir Basu, Daniel Bellm, and Jürgen Werani. Leading Pharmaceutical Operational Excellence: Outstanding Practices and Cases. Springer Berlin / Heidelberg, 2013.

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Friedli, Thomas, Prabir Basu, and Daniel Bellm. Leading Pharmaceutical Operational Excellence: Outstanding Practices and Cases. Springer, 2013.

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Friedli, Thomas, Prabir Basu, Daniel Bellm, and Jürgen Werani. Leading Pharmaceutical Operational Excellence: Outstanding Practices and Cases. Springer, 2016.

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Friedli, Thomas, Prabir Basu, Daniel Bellm, and Jürgen Werani. Leading Pharmaceutical Operational Excellence: Outstanding Practices and Cases. Springer London, Limited, 2013.

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Calnan, Nuala, Martin J. Lipa, Paige E. Kane, and Jose C. Menezes. Lifecycle Approach to Knowledge Excellence in the Biopharmaceutical Industry. Taylor & Francis Group, 2019.

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Calnan, Nuala, Martin J. Lipa, Paige E. Kane, and Jose C. Menezes. Lifecycle Approach to Knowledge Excellence in the Biopharmaceutical Industry. Taylor & Francis Group, 2017.

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Calnan, Nuala, Martin J. Lipa, Paige E. Kane, and Jose C. Menezes. Lifecycle Approach to Knowledge Excellence in the Biopharmaceutical Industry. Taylor & Francis Group, 2017.

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Book chapters on the topic "Pharmaceutical Excellence"

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Kaur, Simran, Shrutika Sharma, Vishesh Sahu, Sandeep Arora, Navneet Sharma, and Vikesh Kumar Shukla. "Advancing Laboratory Excellence." In Understanding Pharmaceutical Standards and Regulations. Routledge, 2025. https://doi.org/10.4324/9781003500971-6.

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Basu, Prabir, Thomas Friedli, and Daniel Bellm. "The Future of Pharmaceutical Manufacturing." In Leading Pharmaceutical Operational Excellence. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-35161-7_29.

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Friedli, Thomas, Fabian Liebetrau, and Richard Luetzner. "Managing Global Pharmaceutical Manufacturing Networks." In Leading Pharmaceutical Operational Excellence. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-35161-7_30.

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Friedli, Thomas, and Nikolaus Lembke. "Structures of Operational Excellence Initiatives." In Leading Pharmaceutical Operational Excellence. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-35161-7_16.

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Friedli, Thomas, and Jürgen Werani. "Leadership Principles & Operational Excellence." In Leading Pharmaceutical Operational Excellence. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-35161-7_21.

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Friedli, Thomas, and Prabir Basu. "Introduction to Leading Operational Excellence: Making OPEX a Competitive Weapon." In Leading Pharmaceutical Operational Excellence. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-35161-7_1.

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Dreamer, Steve, and Pav Niewiarowski. "Lean in Novartis Pharma: Sustainability Through a Five Step Deployment Methodology." In Leading Pharmaceutical Operational Excellence. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-35161-7_10.

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Starke, Valentin, and Joseph Kumor. "Abbott Pharmaceuticals Journey of Business Excellence Standards." In Leading Pharmaceutical Operational Excellence. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-35161-7_11.

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Troy, Wright. "Structuring and Implementing an Operational Excellence Program from Scratch in the Biotech Industry." In Leading Pharmaceutical Operational Excellence. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-35161-7_12.

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Werani, Jürgen, Volker Pfahlert, Kai Reimers, and Gert Diederich. "Implementing an OE Strategy on Plant Level." In Leading Pharmaceutical Operational Excellence. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-35161-7_13.

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Conference papers on the topic "Pharmaceutical Excellence"

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White, F. E., G. K. Grossmann, H. Decking, and D. C. Agarwal. "Experience with the Use of Alloy 59 (UNS N06059) in Industrial Applications." In CORROSION 1996. NACE International, 1996. https://doi.org/10.5006/c1996-96433.

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Abstract Alloy 59 (UNS N06059) is a high-chromium, high-molybdenum nickel-base alloy designed to provide the widest possible range of corrosion resistance under both oxidizing and reducing conditions. After its introduction some 6 years ago, it rapidly established itself as the prime alloy for many high-severity applications. Of these, flue gas desulfurization (FGD) systems have become the biggest. Increasingly, however, alloy 59 has found application in many other industries. After briefly recalling the principal properties of alloy 59, the paper describes a number of applications which demon
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Seiler, David A., and Jaclyn M. Sekula. "Applications for Polyvinylidene Fluoride and Its Copolymers for Corrosion Resistance in the Chemical Process Industry." In CORROSION 2008. NACE International, 2008. https://doi.org/10.5006/c2008-08530.

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Abstract Polyvinylidene fluoride (PVDF) based polymer resins have been used for corrosive and chemically aggressive fluid containment since 1964. Original components supplied with this resin were rigid piping, valves &amp; fittings, tanks, linings, and heat shrinkable tubing. As plastic processing technologies grew, additional products were offered such as nozzles, dump tower packing, pumps, flow meters, coatings, filtration membranes, and fabrics. In the 1980’s copolymers of vinylidene fluoride and hexafluoropropylene (HFP) were introduced to compliment the very rigid PVDF product line with a
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Jocić, Dragana, Svetlana Vuksanović Pintar, Maja Pavlović, and Dušanka Krajnović. "Historical evolution of training and skills development at BENU Pharmacies." In 46th INTERNATIONAL CONGRESS FOR THE HISTORY OF PHARMACY. Pharmaceutical Association of Serbia, 2024. http://dx.doi.org/10.46793/ishp46.055j.

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The evolution of training and skills development at BENU Pharmacies represents a remarkable journey characterized by strategic foresight and adaptability within the rapidly evolving pharmaceutical industry. Since its inception, BENU Pharmacies has exemplified a strong commitment to operational excellence and workforce development through a meticulously structured approach to training (1-3). Training and development are essential components of organizational success, particularly in industries as dynamic and regulated as pharmaceuticals (4). The ability to continuously enhance both technical an
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Muhammad Khzr Al-Sabawy, Younis, Naji Abdulasattar Mahmood, and Yousif Obed Hama Ameen. "The pillars of knowledge management and its role in enhancing the dimensions of the competitive spectrum : Exploratory study in pharmaceutical companies in the city of Sulaymaniyah (pioneer company and Rasan company) as a model." In 11th International Conference of Economic and Administrative Reform: Necessities and Challenges. University of Human Development, 2022. http://dx.doi.org/10.21928/uhdicearnc/12.

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The research aims to diagnose the contribution of the pillars of knowledge management with its main dimensions (cognitive leadership, organizational structure, learning, technology, knowledge sharing), in enhancing the dimensions of the competitive spectrum represented by (cost leadership strategy, differentiation strategy, and response strategy), to express the ability of organizations In reaching a comprehensive and focused vision that contributes to extracting and deducing the main contents of the dimensions of the competitive spectrum through which it is possible to improve performance and
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Muhammad Khzr Al-Sabawy, Younis, Naji Abdulasattar Mahmood, and Yousif Obed Hama Ameen. "The pillars of knowledge management and its role in enhancing the dimensions of the competitive spectrum : Exploratory study in pharmaceutical companies in the city of Sulaymaniyah (pioneer company and Rasan company) as a model." In 11th International Conference of Economic and Administrative Reform: Necessities and Challenges. University of Human Development, 2022. http://dx.doi.org/10.21928/icearnc/12.

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The research aims to diagnose the contribution of the pillars of knowledge management with its main dimensions (cognitive leadership, organizational structure, learning, technology, knowledge sharing), in enhancing the dimensions of the competitive spectrum represented by (cost leadership strategy, differentiation strategy, and response strategy), to express the ability of organizations In reaching a comprehensive and focused vision that contributes to extracting and deducing the main contents of the dimensions of the competitive spectrum through which it is possible to improve performance and
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Sturgeon, I. L., and J. B. Thomson. "Application of Best Practice Manufacturing Methodologies to Support Achievement of Planned Decommissioning Timescales and Costs." In ASME 2003 9th International Conference on Radioactive Waste Management and Environmental Remediation. ASMEDC, 2003. http://dx.doi.org/10.1115/icem2003-4625.

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The decommissioning of major nuclear plant facilities will inevitably involve a number of project areas where significant levels of processing and manufacturing tasks are required. Typically this includes key task areas such as: • ILW materials retrievals and handling; • ILW / LLW materials processing and encapsulation; • Contaminated surfaces remediation; • Import of materials at dedicated ILW Stores. All such areas involve a series of high level project stages: 1) Design, install and commission facilities; 2) Operate facilities to complete the project tasks (retrievals, processing etc); 3) P
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Barham, Joshua Philip, Yasuo Norikane, Hiromichi Egami, and Yoshitaka Hamashima. "High Efficiency Microwave Flow Chemistry Towards Synthesis of Functional Materials and Pharmaceutical Cores." In Ampere 2019. Universitat Politècnica de València, 2019. http://dx.doi.org/10.4995/ampere2019.2019.9860.

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Microwave (MW) heating benefits organic synthesis by affording higher product yields in shorter time periods than conventional heating, yet it suffers from poor scalability and is limited to polar solvents in typical batch mode reactors. Herein, we report a microwave flow reactor using a solid-state semiconductor MW generator. The tunable, single-mode MW heating allows high efficiency, scalable organic synthesis, rapid reaction optimization and is applicable to non-polar solvents (o-Xylene and CPME can be rapidly heated to ca. 260 oC). Auto-frequency tuning compensates for changes in the micro
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Gheorghita, Roxana, Roxana Filip, and Anderi Lobiuc. "NOVEL MATERIALS WITH MICROENCAPSULATED ESSENTIAL OILS, POTENTIAL APPLICATIONS FOR SKIN CELLULAR REGENERATION DRESSINGS." In 23rd SGEM International Multidisciplinary Scientific GeoConference 2023. STEF92 Technology, 2023. http://dx.doi.org/10.5593/sgem2023v/6.2/s24.60.

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Biopolymers have gained notoriety due to their unique physical, chemical, and mechanical characteristics and performances. Due to their regenerability, compostability, biocompatibility, non-immunogenic, non-toxic, or non-allergenic properties, they have surpassed the boundaries of the food industry and have become fundamental components in biomedicine or the pharmaceutical industry. Thus, the most well-known applications are as drug delivery systems, tissue engineering, or wound dressings. In addition to all these characteristics, biopolymeric films have proven to be excellent matrices for inc
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Letsiou, Sophia, Apostolos Beloukas, Efstathios Rallis, and Vasiliki Kefala. "In vitro skin models. Challenges and Future Steps." In 1st Conference of the Hellenic Scientific Society of Aesthetics. PHARMAKON-Press, 2024. http://dx.doi.org/10.61873/fcxv3865.

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The in vitro models have great potential in skin-related research as well as in testing for active ingredients in cosmetics, dermocosmetics and pharmaceuticals. Human skin behavior can be simulated in vitro using a variety of methods ranging from cell monolayer models to complicated organotypic and bioengineered three-dimensional models. Moreover, skin in vitro models offer an excellent alternative to animal testing in cosmetics and some of them are validated to be used as preclinical as-says. However, the in vitro simulation of the whole skin together with its appendages is still in its early
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Grinco, Marina, Alexandru Marina, Natalia Birca, et al. "Pomolic acid from apple pomace: quantitative determination by heteronuclear two-dimentional QNMR and preparative isolation." In Scientific seminar with international participation "New frontiers in natural product chemistry". Institute of Chemistry, Republic of Moldova, 2023. http://dx.doi.org/10.19261/nfnpc.2023.ab14.

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Pomolic acid (PA) is a pentacyclic triterpenic acid isolated from apples by Brieskorn and Wunderer in 1967 [1]. Its highly relevant biological activity profile came recently into focus and there have been many reports on the content of PA in different plant sources [2]. Quite surprisingly, the general perception of low PA content in plants persists and this information hinders its broader investigation as a compound of pharmaceutical and nutraceutical potential. The main aim of the current work was quantitative determination of pomolic acid in apple pomace by two-dimensional heteronuclear NMR
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Reports on the topic "Pharmaceutical Excellence"

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Ssebibubbu, Stuart, Moses Mulumba, Monalisa Chafewa, Maria Birungi, Nimrod Muhumuza, and Baguma Christopher. Analyzing the Capacities of National Medicines Regulatory Agencies To Regulate Vaccine Manufacturing in Africa. Afya na Haki, 2023. http://dx.doi.org/10.63010/k8nm.

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Pharmaceutical production and high-quality medical treatment require effective regulation. National Medicines Regulatory Authorities (NMRAs) oversee medicinal product manufacture, distribution, and sale. Analysing African NMRA capacity is necessary to identify gaps and improve regulatory mechanisms to ensure vaccination quality and public health. This paper employs qualitative methodology to analyze the legal, regulatory, and policy framework systems, which includes a desk review of relevant literature, a writing workshop, and key informant interviews as data sources in Eight countries, includ
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Uche, Chidi, Zita Ekeocha, Stephen Robert Byrn, and Kari L. Clase. Retrospective Study of Inspectors Competency in the Act of Writing GMP Inspection Report. Purdue University, 2021. http://dx.doi.org/10.5703/1288284317445.

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The research was a retrospective study of twenty-five Good Manufacturing Practice (GMP) inspection reports (from March 2017 through to December 2018) of a national medicine regulatory agency, drug Inspectorate, in West Africa, designed to assess the inspectors’ expertise in the act of inspection report writing. The investigation examined a paper-based tool of thirteen pre-registration Inspection reports and twelve GMP reassessment reports written prior and following an intervention program by external GMP trainers to enhance inspectors’ skill in pharmaceutical cGMP inspection. The study made u
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