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Medical Innovation

Medical Innovation

Autor: Kevin E. Behrns , Bruce Gingles , Michael Gregory Sarr

Número de Páginas: 288

Medical Innovation: Concept to Commercialization is a practical, step-by-step approach on how to move a novel concept through development to realize a commercially successful product. Real-world experience cases and knowledgeable contributors provide lessons that cover the practices of diverse organizations and multiple products. This important reference will help improve success and avoid innovation failure for translational researchers, entrepreneurs, medical school educators, biomedical engineering students and faculty, and aspiring physicians. - Provides multiple considerations and comprehensive lessons from varied organizations, researchers and products - Designed to help address topics that improve success and avoid the high cost of innovation failure - Recommends the practical steps needed to move a novel, non-developed concept into a tangible, realistic and commercially successful product

The Modern Ayurveda

The Modern Ayurveda

Autor: C. P. Khare , Chandra Kant Katiyar

Número de Páginas: 417

The Indian population has used Ayurvedic herbs for centuries, but now modern scientific work has led to recognition and acceptance at a global level. The major cause of the increased popularity of Ayurvedic medicine stems from recent scientific validation and its potential in lifestyle management. This growth in research in India and worldwide has created the need for a resource covering the scientific development of Ayurvedic herbs for practice during the postclassical period. The Modern Ayurveda: Milestones Beyond the Classical Age explores a host of topics essential to understanding the surge of scientific work now being conducted on this ancient practice. A one-point source for the modern explorer attempting to appreciate the transformation of Ayurveda from an empirical to a rationalist understanding, the book enumerates more than 400 Ayurvedic herbs with compiled information including their botanical name, common Ayurvedic name and family, their attributes, chemical constituents, phytochemical markers, pharmacological actions, and their interactions and toxicity. It explores current research methodologies for the evaluation of efficacy and safety of herbal medicine and...

Modern Biopharmaceuticals

Modern Biopharmaceuticals

Autor: Jörg Knäblein

Número de Páginas: 724

This collection of high-profile contributions provides a unique insight into the development of novel, successful biopharmaceuticals. Outstanding authors, including Nobel laureate Robert Huber as well as prominent company researchers and CEOs, present valuable insider knowledge, limiting their scope to those procedures and developments with proven potential for the biotechnology industry. They cover all relevant aspects, from the establishment of biotechnology parks, the development of successful compounds and the implementation of efficient manufacturing processes, right up to the establishment of advanced delivery routes.

Surgery and Operating Room Innovation

Surgery and Operating Room Innovation

Autor: Seiichi Takenoshita , Hiroshi Yasuhara

Número de Páginas: 129

This book presents cutting-edge surgical techniques and the new operating rooms supporting them, as well as their future developments. In recent years, with the advances in surgical medicine, surgical techniques have undergone great changes. However, safety and reliability are still the major requirements of the operating room, and these are closely linked to the patients’ wellbeing. The new medical instruments and medical materials being developed to perform surgery more safely, reliably and efficiently are vital technologies supporting this. “New techniques” involve the introduction of innovative medical instruments and medical materials, and these, too, are increasing in terms of performance and size every year. Surgery and Operating Room Innovation discusses these issues from the perspective of various professionals involved with operating rooms.

Innovation in America

Innovation in America

Autor: United States. Congress. Senate. Committee On Commerce, Science, And Transportation. Subcommittee On Competitiveness, Innovation, And Export Promotion

Número de Páginas: 90
Innovation and Invention in Medical Devices

Innovation and Invention in Medical Devices

Autor: Institute Of Medicine , Board On Health Sciences Policy , Roundtable On Research And Development Of Drugs, Biologics, And Medical Devices

Número de Páginas: 112

The objective of the workshop that is the subject of this summary report was to present the challenges and opportunities for medical devices as perceived by the key stakeholders in the field. The agenda, and hence the summaries of the presentations that were made in the workshop and which are presented in this summary report, was organized to first examine the nature of innovation in the field and the social and economic infrastructure that supports such innovation. The next objective was to identify and discuss the greatest unmet clinical needs, with a futuristic view of technologies that might meet those needs. And finally, consideration was given to the barriers to the application of new technologies to meet clinical needs.

Biomaterials Innovation

Biomaterials Innovation

Autor: Alexander Styhre

Número de Páginas: 221

Rapid advances in the life sciences means that there is now a far more detailed understanding of biological systems on the cellular, molecular and genetic levels. Sited at the intersection between the life sciences, the engineering sciences and the des

Promoting access to medical technologies and innovation

Promoting access to medical technologies and innovation

Número de Páginas: 352

The revised study records the numerous significant developments that we have seen since 2013. These include efforts made towards achieving universal health coverage, challenges posed by antimicrobial resistance, the changing disease burden and new global disease threats. The study reviews public and private sector innovation models, as well as the repercussions of an increasingly diverse medical technologies industry and the rise of innovative and production capacity in developing countries. It draws practical lessons from experiences regarding how public health, IP, trade and competition rules all interact with each other in the broader context of the human rights dimension of health and the United Nations' Sustainable Development Goals (SDGs). And it provides insights on measures to promote innovation and access to medical technologies, noting the growing network of free trade agreements and the importance that trade plays for access to medical technologies.

Modern Medicine

Modern Medicine

Autor: Pronobesh Chattopadhyay , Danswrang Goyary

Número de Páginas: 265

Modern Medicine: Biomedical Devices, Medical Gases, Radiopharmaceuticals, New Drug Discovery, Volume 2 discusses the procedures of drug approval and regulatory requirements that must be met according to the United States Food and Drug Administration (FDA), the European Medical Agency (EMA), and the Central Drug Standard Control Organization (CDSCO). In the rapidly evolving landscape of modern medicine, groundbreaking innovations have emerged that are reshaping the way we approach healthcare. Modern Medicine delves into the cutting-edge realms of medical devices, medical gases, radiopharmaceuticals, and new drug discovery, offering a comprehensive exploration of these transformative fields that are revolutionizing patient care and medical practices. Discover the future of healthcare technology, and uncover the intricate world of biomedical engineering, where state-of-the-art devices seamlessly merge with the human body to monitor, diagnose, and treat ailments Dive deep into the utilization of medical gases for respiratory conditions, pain management, and even novel applications in regenerative medicine Unravel the mysteries of radiopharmaceuticals, a fusion of molecular imaging and ...

FDA User Fee Agreements: Improving Medical Product Regulation and Innovation for Patients, Part 1, S.HRG. 115-255, March 21, 2017, 115-1

FDA User Fee Agreements: Improving Medical Product Regulation and Innovation for Patients, Part 1, S.HRG. 115-255, March 21, 2017, 115-1

Número de Páginas: 84
Social, Technological and Health Innovation: Opportunities and Limitations for Social Policy, Health Policy, and Environmental Policy

Social, Technological and Health Innovation: Opportunities and Limitations for Social Policy, Health Policy, and Environmental Policy

Autor: Andrzej Klimczuk , Magdalena Klimczuk-kochańska , Jorge Felix

Número de Páginas: 159

Abstract: This Research Topic focuses on both strengths and weaknesses of social innovation, technological innovation, and health innovation that are increasingly recognized as crucial concepts related to the formulation of responses to the social, health, and environmental challenges. Goals of this Research Topic: (1) to identify and share the best recent practices and innovations related to social, environmental and health policies; (2) to debate on relevant governance modes, management tools as well as evaluation and impact assessment techniques; (3) to discuss dilemmas in the fields of management, financing, designing, implementing, testing, and maintaining the sustainability of innovative models of delivering social, health and care services; and (4) to recognize and analyze social, technological and health innovation that has emerged or has been scaled-up to respond to crisis situations, for example, a pandemic of the COVID-19 coronavirus disease

Regulatory Aspects of Gene Therapy and Cell Therapy Products

Regulatory Aspects of Gene Therapy and Cell Therapy Products

Autor: Maria Cristina Galli

Número de Páginas: 243

This book discusses the different regulatory pathways for Advanced Therapy Medicinal Products implemented by national agencies in North and South America, Europe and Asia and by international bodies in the effort of international harmonization. This book represents an update of the first edition, as it covers regulatory novelties and accumulated experience in the regions already addressed. In addition, this new edition offers a wider international perspective: new chapters are included covering Advanced Therapy Medicinal Products regulations in India, Malaysia, Spain and Thailand, the European Pharmacopoeia texts for gene therapy medicinal products as well as international harmonization programs. Each chapter, authored by experts from various regulatory bodies throughout the international community, walks the reader through the applications of nonclinical research to translational clinical research to licensure and therapeutic use of these innovative products. More specifically, each chapter offers insights into fundamental considerations that are essential for developers of Advanced Therapy Medicinal Products in the areas of product quality, pharmacology and toxicology, clinical...

The Business of Healthcare Innovation

The Business of Healthcare Innovation

Autor: Lawton R. Burns

Número de Páginas: 400

The Business of Healthcare Innovation is the first wide-ranging analysis of business trends in the manufacturing segment of the health care industry. In this leading edge volume, Professor Burns focuses on the key role of the 'producers' as the main source of innovation in health systems. Written by professors of the Wharton School and industry executives, this book provides a detailed overview of the pharmaceutical, biotechnology, genomics/proteomics, medical device and information technology sectors. It analyses the market structures of these sectors as well as the business models and corporate strategies of firms operating within them. Most importantly, the book describes the growing convergence between these sectors and the need for executives in one sector to increasingly draw upon trends in the others. It will be essential reading for students and researchers in the field of health management, and of great interest to strategy scholars, industry practitioners and management consultants.

Medical Innovation

Medical Innovation

Autor: Davide Consoli , Andrea Mina , Richard R. Nelson , Ronnie Ramlogan

Número de Páginas: 213

This book brings together a collection of empirical case studies featuring a wide spectrum of medical innovation. While there is no unique pathway to successful medical innovation, recurring and distinctive features can be observed across different areas of clinical practice. This book examines why medical practice develops so unevenly across and within areas of disease, and how this relates to the underlying conditions of innovation across areas of practice. The contributions contained in this volume adopt a dynamic perspective on medical innovation based on the notion that scientific understanding, technology and clinical practice co-evolve along the co-ordinated search for solutions to medical problems. The chapters follow an historical approach to emphasise that the advancement of medical know-how is a contested, nuanced process, and that it involves a variety of knowledge bases whose evolutionary paths are rooted in the contexts in which they emerge. This book will be of interest to researchers and practitioners concerned with medical innovation, management studies and the economics of innovation. Chapter 5 of this book is freely available as a downloadable Open Access PDF at ...

The Innovation and Evolution of Medical Devices

The Innovation and Evolution of Medical Devices

Autor: S. Abbas Shobeiri

Número de Páginas: 314

This text provides a central resource for physicians, entrepreneurs, and the MBA students about how innovation occurs in medical device industry. The book uses the rise and fall of vaginal mesh kits to highlight the evolution of responses by the physicians, patients and the regulatory bodies. There are specific chapters reviewing the US regulatory issues and business practices that were consequential to withdrawal of most vaginal mesh kits from the US market. The book is meant to be concise, evidence-based, and practical for the first time readers to understand the innovation forces. Concise textual information from acknowledged experts is complemented by high-quality diagrams and images to provide a thorough update of this rapidly evolving medical device industry. The case study chapters fully elucidate the anatomical basis that led to conceptualization of vaginal mesh kits, their introduction into the market, medicolegal and business implications followed with innovation that occurred by the surgeons to utilize ultrasound for and innovative surgeries to overcome device complications. With a luxurious number of well-marked pictures, readers will gain a clear understanding of the...

Medical devices made of substances for human health: A challenge in terms of efficacy, safety and sustainability

Medical devices made of substances for human health: A challenge in terms of efficacy, safety and sustainability

Autor: Juan L. Tamargo , Alessandro Mugelli

Número de Páginas: 66
Modern Biopharmaceuticals, 4 Volume Set

Modern Biopharmaceuticals, 4 Volume Set

Autor: Jörg Knäblein

Número de Páginas: 2074

The biopharmaceutical market has come along way since 1982 when the first biopharmaceutical product, recombinant human insulin, was launched. Over 120 such products are currently being marketed around the world including nine blockbuster drugs. The global market for biopharmaceuticals, which is currently valued at US$41 billion, has been growing at an impressive compound annual growth rate of 21% over the previous five years. With over one third of all pipe-line products in active development are biopharmaceuticals, this segment is set to continue outperforming the total pharmaceutical market and could easily reach US$100 billion by the end of this decade.

Formulating Pharma-, Nutra-, and Cosmeceutical Products from Herbal Substances

Formulating Pharma-, Nutra-, and Cosmeceutical Products from Herbal Substances

Autor: Anupama Singh , Hitesh Kulhari , Vikas Anand Saharan

Número de Páginas: 820

A practical and up-to-date discussion of the formulation and design of dosage forms and delivery systems containing herbal ingredients In Formulating Pharma-, Nutra-, and Cosmeceutical Products from Herbal Substances: Dosage Forms and Delivery Systems, a team of distinguished researchers delivers a step-by-step approach to preparing and manufacturing dosage forms and delivery systems. Intuitively organized with comprehensive coverage of the fundamentals, functional materials, manufacturing, and marketing of pharmaceutical, nutraceutical, and cosmeceutical products, the book also examines regulatory issues of quality, safety, and efficacy. The authors discuss essential formulation development and delivery information for novel and controlled delivery systems of herbal ingredients. Readers will also find: A thorough introduction to the basic principles of developing modern pharma-, nutra-, and cosmeceutical products from herbal substances Comprehensive explorations of conventional formulations, including issues of stability Practical discussions of advanced formulations, including chronotherapeutic delivery systems, liposome-based delivery of phytoconstituents, and nanoparticle...

Natural Products as Sources of Innovative Approaches in Psychiatry

Natural Products as Sources of Innovative Approaches in Psychiatry

Autor: Elaine Elisabetsky , Chun-tao Che , Elizabeth Anne Olson , Zhang-jin Zhang

Número de Páginas: 158
Medical Regulatory Affairs

Medical Regulatory Affairs

Autor: Jack Wong , Raymond Tong

Número de Páginas: 978

This handbook covers medical device regulatory systems in different countries, ISO standards for medical devices, clinical trial and regulatory requirements, and documentation for application. It is the first to cover the medical device regulatory affairs in Asia. Experts from influential international regulatory bodies, including the US Food and Drug Administration (FDA), UK Medicines and Healthcare Products Regulatory Agency, Japan Pharmaceuticals and Medical Devices Agency, Saudi Food and Drug Authority, Korea Testing Laboratory, Taiwan FDA, World Health Organization, Asian Harmonization Working Party, Regulatory Affairs Professionals Society, and British Standards Institution, have contributed to the book. Government bodies, the medical device industry, academics, students, and general readers will find the book immensely useful for understanding the global regulatory environment and in their research and development projects. The updated fourth edition includes specific contributions that address the needs of startups.

Medical Devices

Medical Devices

Autor: World Health Organization

Número de Páginas: 147

Background papers 1 to 9 published as technical documents. Available in separate records from WHO/HSS/EHT/DIM/10.1 to WHO/HSS/EHT/DIM/10.9

Handbook of Modern Hospital Safety

Handbook of Modern Hospital Safety

Autor: William Charney

Número de Páginas: 1252

It is ironic that those whose job it is to save lives often find themselves injured in the course of performing their duties. In fact, according to the Bureau of Labor Statistics, healthcare workers have higher injury rates than agriculture workers, miners, and construction workers. The Handbook of Modern Hospital Safety, Second Edition covers expo

The Combination Products Handbook

The Combination Products Handbook

Autor: Susan Neadle

Número de Páginas: 438

Combination products are therapeutic and diagnostic products that combine drugs, devices, and/or biological products. According to the US Food and Drug Administration (FDA), “a combination product is one composed of any combination of a drug and a device; a biological product and a device; a drug and a biological product; or a drug, device and a biological product.” Examples include prefilled syringes, pen injectors, autoinjectors, inhalers, transdermal delivery systems, drug-eluting stents, and kits containing drug administration devices co-packaged with drugs and/or biological products. This handbook provides the most up-to-date information on the development of combination products, from the technology involved to successful delivery to market. The authors present important and up-to-the-minute pre- and post-market reviews of international combination product regulations, guidance, considerations, and best practices. This handbook: Brings clarity of understanding for global combination products guidance and regulations Reviews the current state-of-the-art considerations and best practices spanning the combination product lifecycle, pre-market through post-market Reviews...

An Overview of FDA Regulated Products

An Overview of FDA Regulated Products

Autor: Eunjoo Pacifici , Susan Bain

Número de Páginas: 386

An Overview of FDA Regulated Products: From Drugs and Cosmetics to Food and Tobacco, Second Edition is fully updated to reflect recent advances in science and technology and new laws and regulations. Breakthroughs in cellular and gene therapy, immunotherapy, precision medicine, and digital health are changing the face of healthcare and regulation. The updates brought about by the 21st Century Cures Act and subsequent PDUFA Reauthorizations, as well as signing into law the "Modernization of Cosmetic Regulation Act of 2022," which will transform FDA's oversight of cosmetics, are fully reflected in all chapters of the book.This book provides graduate students and industry professionals with comprehensive information on approval processes with the FDA and other country regulation organizations. Regulatory science professionals working with not only drugs, but biologics, medical devices, food and additives, cosmetics, veterinary products, and tobacco will benefit from this comprehensive overview of the regulatory environment. - Provides an in-depth overview on how drugs, cosmetics, food, and tobacco products are regulated by the FDA and agencies around the world - Includes chapters...

Clinical Translation and Commercialisation of Advanced Therapy Medicinal Products

Clinical Translation and Commercialisation of Advanced Therapy Medicinal Products

Autor: Tracy Tong Li Yu , Yves Bayon , Alain A. Vertes , Ivan Martin

Número de Páginas: 175

Dr. Yves Bayon is a Senior Principal Scientist at Medtronic and Dr. Alain Vertes is affiliated with NxR Biotechnologies GmbH. All other Topic Editors declare no competing interests with regards to the Research Topic subject.

Artificial Intelligence in Medical Imaging in China

Artificial Intelligence in Medical Imaging in China

Autor: Shiyuan Liu

Número de Páginas: 448

This book overviews the latest development of Artificial Intelligence in medical imaging in China. Consisted of thirteen chapters, this book discusses development, status, achievements, prospects, visions, bottlenecks, and future challenges affecting development of artificial intelligence in medical imaging from different aspects of government supervision, industrialization, education, academic research and application implementation. It will facilitate better communication between China and foreign countries in all directions of medical imaging AI for all stakeholders.

Collaborative Innovation in Drug Discovery

Collaborative Innovation in Drug Discovery

Autor: Rathnam Chaguturu

Número de Páginas: 768

Can academia save the pharmaceutical industry? The pharmaceutical industry is at a crossroads. The urgent need for novel therapies cannot stem the skyrocketing costs and plummeting productivity plaguing R&D, and many key products are facing patent expiration. Dr. Rathnam Chaguturu presents a case for collaboration between the pharmaceutical industry and academia that could reverse the industry's decline. Collaborative Innovation in Drug Discovery: Strategies for Public and Private Partnerships provides insight into the potential synergy of basing R&D in academia while leaving drug companies to turn hits into marketable products. As Founder and CEO of iDDPartners, focused on pharmaceutical innovation, Founding president of the International Chemical Biology Society, and Senior Director-Discovery Sciences, SRI International, Dr. Chaguturu has assembled a panel of experts from around the world to weigh in on issues that affect the two driving forces in medical advancement. Gain global perspectives on the benefits and potential issues surrounding collaborative innovation Discover how industries can come together to prevent another "Pharma Cliff" Learn how nonprofits are becoming the...

Where to from here: Advancing patient and public involvement in health technology assessment (HTA) following the COVID-19 pandemic

Where to from here: Advancing patient and public involvement in health technology assessment (HTA) following the COVID-19 pandemic

Autor: Janet L. Wale , Sally Wortley , Marie-pascale Pomey

Número de Páginas: 87
Clinical and Translational Science

Clinical and Translational Science

Autor: David Robertson , Gordon H. Williams

Número de Páginas: 812

Clinical and Translational Science: Principles of Human Research, Second Edition, is the most authoritative and timely resource for the broad range of investigators taking on the challenge of clinical and translational science, a field that is devoted to investigating human health and disease, interventions, and outcomes for the purposes of developing new treatment approaches, devices, and modalities to improve health. This updated second edition has been prepared with an international perspective, beginning with fundamental principles, experimental design, epidemiology, traditional and new biostatistical approaches, and investigative tools. It presents complete instruction and guidance from fundamental principles, approaches, and infrastructure, especially for human genetics and genomics, human pharmacology, research in special populations, the societal context of human research, and the future of human research. The book moves on to discuss legal, social, and ethical issues, and concludes with a discussion of future prospects, providing readers with a comprehensive view of this rapidly developing area of science. Introduces novel physiological and therapeutic strategies for...

Medical Devices and Equipment Competitive Conditions Affecting U.S. Trade in Japan and Other Principal Foreign Markets, Inv. 332-474

Medical Devices and Equipment Competitive Conditions Affecting U.S. Trade in Japan and Other Principal Foreign Markets, Inv. 332-474

Número de Páginas: 180
Novel Therapeutics from Modern Biotechnology

Novel Therapeutics from Modern Biotechnology

Autor: Dale L. Oxender , Leonard E. Post

Número de Páginas: 261

A cover story of Business Week Magazine in January 1984 stated "Biotech Comes of Age". In February 1986, Venture Magazine had a cover article entitled "The Biotech Revolution is Here". This article went on to say "New Genetic Technologies Will Transform Our Lives". These announcements were made many years after the first biotechnology companies, such as Genentech, Cetus, Amgen and Biogen, were formed-to commercialize the "New Biology". . At the time of writing this book, there are over 1300 biotech companies developing new technologies or identifying potential biotech drugs. Most of these companies were started in the height of the "high-technology hype", although companies are still forming as the technology advances. A more recent survey showed only a relatively small number of Food and Drug Administration (FDA) approvals among over several hundred biotech nology products now in clinical trial. One could ask why it has taken so long to produce biotechnology products. Part of the reason is that each new class of biotech products brings with it a set of problems that need to be solved before they enter clinical trials. These problems are often unique to biotechnology products,...

Towards continued and affordable accessibility of innovative drugs: Sustainable development and efficient use of medicines

Towards continued and affordable accessibility of innovative drugs: Sustainable development and efficient use of medicines

Autor: Sahar Barjesteh Van Waalwijk Van Doorn-khosrovani , Rob Ter Heine , Atse Huisman , Denise Van Den Berg , Bettina Ryll , Maria Judit Molnar , Saco De Visser

Número de Páginas: 143

The rising costs of medicines is a major burden for healthcare systems and is already limiting access to innovative treatments worldwide. Governments, healthcare providers and payers constantly try to improve the sustainability of drug development, production, pricing and use of medicines. The aim of this research topic is to identify strategies and policies that can facilitate sustainable development and use of medicines as well as practical solutions to improve their cost-effectiveness. For this topic, we are also interested in alternative pricing strategies and financial arrangements, requisite changes in regulatory and legal frameworks to support sustainability, the potential role of registries, real-world evidence and biomarker development for clinical daily use. The submissions (Original research/Reviews/Mini-reviews/Perspectives/Clinical Studies) may refer to, but are not limited to, manuscripts involving: 1. Dose-rounding, dose-banding or vial-sharing to minimise the wasting of expensive medicines 2. Alternative dosing strategies, such as tapering and/or increasing the dose-interval or shortening treatment duration 3. Boosting potency of drugs 4. The use of predictive...

Drug Delivery Systems Principles & Innovations in Pharmaceutical Formulations

Drug Delivery Systems Principles & Innovations in Pharmaceutical Formulations

Autor: Mr. Darshan Lalwani , Dr. Kanchan Bhasin , Dr. Ashish Yashwantrao Pawar

Número de Páginas: 321

The book, explores the evolution, types, and current trends in drug delivery. It covers foundational concepts of drug delivery systems (DDS), focusing on techniques designed to maximize therapeutic efficacy and patient compliance. Through in-depth discussions on diverse delivery methods such as oral, transdermal, and nanotechnology-based systems, the book examines the challenges and innovations in targeting specific cells and sustaining drug release. With special emphasis on case studies, personalized medicine, and ethical considerations, it also highlights regulatory guidelines and future directions for drug delivery in modern healthcare. This comprehensive guide serves as a crucial resource for professionals in pharmaceutical science, providing insights into the advancements and complexities of DDS technology in optimizing patient outcomes.

Multipurpose Prevention Technologies: Call for Innovative Strategies to Address Critical Priorities and Gaps

Multipurpose Prevention Technologies: Call for Innovative Strategies to Address Critical Priorities and Gaps

Autor: Bethany Young Holt , Z. Mike Chirenje , Nomita Chandhiok , Ariane Van Der Straten , Jim Turpin , Anke Hemmerling

Número de Páginas: 116

The HIV/sexually transmitted infection (STI) syndemics and the unmet need for modern contraceptive methods continue to pose significant health risks for women and other people worldwide. As awareness of the need to address these interlinked risks has increased, the need for new technologies that combine protection against unintended pregnancy, HIV and other STIs is a growing research priority. Multipurpose Prevention Technologies (MPTs) are products that simultaneously prevent HIV, other STIs, and/or unintended pregnancy. They have power to revolutionize women's health by providing prevention for multiple indications.

Medical Procedures Innovation and Affordability Act and Inventor Protection Act of 1995

Medical Procedures Innovation and Affordability Act and Inventor Protection Act of 1995

Autor: United States. Congress. House. Committee On The Judiciary. Subcommittee On Courts And Intellectual Property

Número de Páginas: 140

Distributed to some depository libraries in microfiche.

Research Handbook on Innovation in International Business

Research Handbook on Innovation in International Business

Autor: Dikova, Desislava , Ipsmiller, Edith

Número de Páginas: 315

Expansive and engaging, the Research Handbook on Innovation in International Business takes a deep dive into technological, organisational, firm, and industry-level innovation. Contributions from leading experts in international business cover large multinational firms to SMEs and emerging markets, providing industry-specific insights into innovative solutions from across the globe.

Innovative Medical Technology Based on Artificial Cells, Including its Different Configurations

Innovative Medical Technology Based on Artificial Cells, Including its Different Configurations

Autor: Thomas Ming Swi Chang , Binglan Yu

Número de Páginas: 148

Artificial Cells are not to reproduce biological cells but to prepare an artificial system for possible uses in medicine and other areas. Many of the ideas on artificial cells are being extensively applied and extended by researchers worldwide, resulting in rapid and exciting progress and discoveries. Different configurations include using emulsion methods and microfluidizers to form microscopic or nano dimension cells called artificial cells, synthetic cells, microcapsules, nanocapsules, liposomes, microparticles, nanoparticles, polymersomes, etc. Macro dimensions artificial cells are used for bioencapsulated cells. Soluble nanobiotherapeutics can be formed by crosslinking proteins and enzymes or by PEG conjugation. The principle of artificial cell has now evolved into nanomedicine, biotherapeutics, blood substitutes, drug delivery, enzyme/gene therapy, cancer therapy, cell/stem cell therapy, nanoparticles, liposomes, bioencapsulation, replicating synthetic cells, cell encapsulation, biosorbent/immunosorbent hemoperfusion/plasmapheresis, regenerative medicine, encapsulated microbe, COVID_19 vaccine, COVID_19 therapy, nanobiotechnology, nanotechnology and other areas.

Innovations in Modeling and Simulation to Advance Translational Science

Innovations in Modeling and Simulation to Advance Translational Science

Autor: Melissa Knothe Tate , Leonardo Angelone , Christopher Basciano , Markus Reiterer

Número de Páginas: 191

This eBook is a collection of articles from a Frontiers Research Topic. Frontiers Research Topics are very popular trademarks of the Frontiers Journals Series: they are collections of at least ten articles, all centered on a particular subject. With their unique mix of varied contributions from Original Research to Review Articles, Frontiers Research Topics unify the most influential researchers, the latest key findings and historical advances in a hot research area! Find out more on how to host your own Frontiers Research Topic or contribute to one as an author by contacting the Frontiers Editorial Office: frontiersin.org/about/contact.

Innovation Strategy for Enterprises in Emerging Economies

Innovation Strategy for Enterprises in Emerging Economies

Autor: Anurag Satpathy , Arjun Agrawal , Sanjay Mohapatra

Número de Páginas: 152

Particularly in developing economies, there is a need for business alignment with innovation strategy and execution of strategies. The authors demonstrate through real-world examples and case studies how a firm can use innovation at all levels (strategic, functional and operational) to provide benefits to the entire value chain.

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