Ethocle Reports has published its latest Market Research Report on Drug Eluting Stents (DES) - Medical Devices Pipeline Assessment, 2016. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Deep Brain Stimulators - Medical Devices Pipeline Assessment, 2016. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Cardiac Valve Repairs. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Ventricular Assist Devices. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Cardiac Valve Repairs - Medical Devices Pipeline Assessment, 2016. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Transcatheter Heart Valves - Medical Devices Pipeline Assessment, 2016. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Advanced Wound Management. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Neurological Diagnostic Equipment - Medical Devices Pipeline Assessment, 2016. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Deep Brain Stimulators - Medical Devices Pipeline Assessment, 2016. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Cardiac Valve Repairs. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Ventricular Assist Devices. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Cardiac Valve Repairs - Medical Devices Pipeline Assessment, 2016. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Transcatheter Heart Valves - Medical Devices Pipeline Assessment, 2016. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Advanced Wound Management. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Neurological Diagnostic Equipment - Medical Devices Pipeline Assessment, 2016. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Peripheral Vascular Stents - Medical Devices Pipeline Assessment, 2016. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Peripheral Vascular Stents - Medical Devices Pipeline Assessment, 2016. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Responding Effectively to FDA 483 Observations & Warning LettersMaetrics
You receive a Warning Letter-- you have 15 days to submit a response. If FDA finds your response inadequate, you may receive a Consent Decree, which will cost millions to remediate. You need a process in place to react to a Warning Letter before it is delivered. These experts will discuss planning, procedures, training and ways to keep from getting a warning letter in the first place.
Previously certain classes of active substances were required to be manufactured in dedicated or segregated self-contained facilities Certain antibiotics, Certain hormones, Certain cytotoxic ,Certain highly active drugs .This was due to the perceived risk of these active substances.
Pharmaceuticals not covered under these criteria were addressed by a cleaning validation process This involved reduction of the concentration of residual active substance to a level where the maximum carryover from the total equipment train would result in no greater than 1/1000th of the lowest clinical dose of the contaminating substance in the maximum daily dosage of the next product to be manufactured.
This criterion was applied concurrently with a maximum permitted contamination of 10 ppm of the previous active substance in the next product manufactured. Whichever of these criteria resulted in the lowest carryover, constituted the limit applied for cleaning validation. However, these limits did not take account of the available pharmacological and toxicological data They may have been too restrictive or not restrictive enough. EMA therefore felt for a more scientific case by case approach for all classes of pharmaceutical substances.
in this slide contains introduction, types, classification, review team, requirement of protocol and process of Investigated New Drug Application (IND).
Presented by: RAVI SHANKAR D (Department of pharmaceutical analysis and quality assurance),
RIPER, anantapur.
http://MedicalDeviceEvents.com At the 10x Medical Device Conference in 2014, presenters Carrie Kuehn, Jorge Ochoa, and Robert Packard explained why, according to data from FDA, more than 58% of 510(k) submissions were refused under FDA’s Refuse to Accept (RTA) policy during its first year of implementation.
This presentation examined some of the reasons why industry got such a bad “grade.” We discussed the RTA requirements and some of the challenges from industry’s perspective on meeting the requirements of the RTA checklist and ended with recommendations on how industry can improve its odds of getting past the RTA hurdle on the first try.
Guangzhou Shuokang, founded 10 years ago, is producing laboratory furniture in our factory in Guangzhou. We have a technical staff which has more than 25 years of experience. The factory dedicated to producing laboratory furniture. Shuokang exports 60% of the production to areas outside of Turkey. The world market is asking for high quality products. The products have to be according international and local standards. We produce the furniture according to different standards. We are monitoring the market to check for standards and look for ways to make or keep our furniture according to these standards. Our factory is, of course, accredited according to ISO 9001 Quality System. Our mission is to help you with your laboratory furniture needs. We don’t want to supply you with a set of furniture but with a laboratory solution.Laboratory comprehensive system engineering: Decoration, ventilation, environmental protect, intelligent engineering design and construction,laboratory cabinets,fume hood and other equipment.
FDA Form 483 (Inspectional Observations) - Top Violations 2013Marc Sanchez
FDA Attorney Marc Sanchez discusses the Top FDA Form 483 (Inspectional Observations) from fiscal year 2013. The top observations provide a foundation for preparing for a pre-inspection, for-cause inspection, or routine surveillance inspection.
New PDA/IPEC Technical Report on Excipient Risk Assessment - insights for dru...MilliporeSigma
Access the interactive recording: https://bit.ly/37HqbTK
Abstract:
Since March 2016 the EU Guideline to ascertain the appropriate GMP for pharmaceutical excipients is legally binding. Although the EU Guideline itself provides a high level description how to perform the risk assessment, the implementation can be challenging. In January 2018 PDA and IPEC formed a joint Task Force with the objective to develop a joint Technical Report to share best practices with industry. This Technical Report was published in December 2019. In this webinar you will be introduced to the new Technical Report, its objective, proposed approaches and examples shared by PDA/IPEC member companies.
Global Markets Direct's, 'Esophageal Cancer - Pipeline Review, H1 2013', provides an overview of the indication's therapeutic pipeline. This report provides information on the therapeutic development for Esophageal Cancer, complete with latest updates, and special features on late-stage and discontinued projects.
https://www.reportscorner.com/reports/23243/Esophageal-Cancer-%E2%80%93-Pipeline-Review,-H1-2013/
Ethocle Reports has published its latest Market Research Report on Transdermal Drug Delivery - Medical Devices Pipeline Assessment, 2016. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Peripheral Vascular Stents - Medical Devices Pipeline Assessment, 2016. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Peripheral Vascular Stents - Medical Devices Pipeline Assessment, 2016. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Responding Effectively to FDA 483 Observations & Warning LettersMaetrics
You receive a Warning Letter-- you have 15 days to submit a response. If FDA finds your response inadequate, you may receive a Consent Decree, which will cost millions to remediate. You need a process in place to react to a Warning Letter before it is delivered. These experts will discuss planning, procedures, training and ways to keep from getting a warning letter in the first place.
Previously certain classes of active substances were required to be manufactured in dedicated or segregated self-contained facilities Certain antibiotics, Certain hormones, Certain cytotoxic ,Certain highly active drugs .This was due to the perceived risk of these active substances.
Pharmaceuticals not covered under these criteria were addressed by a cleaning validation process This involved reduction of the concentration of residual active substance to a level where the maximum carryover from the total equipment train would result in no greater than 1/1000th of the lowest clinical dose of the contaminating substance in the maximum daily dosage of the next product to be manufactured.
This criterion was applied concurrently with a maximum permitted contamination of 10 ppm of the previous active substance in the next product manufactured. Whichever of these criteria resulted in the lowest carryover, constituted the limit applied for cleaning validation. However, these limits did not take account of the available pharmacological and toxicological data They may have been too restrictive or not restrictive enough. EMA therefore felt for a more scientific case by case approach for all classes of pharmaceutical substances.
in this slide contains introduction, types, classification, review team, requirement of protocol and process of Investigated New Drug Application (IND).
Presented by: RAVI SHANKAR D (Department of pharmaceutical analysis and quality assurance),
RIPER, anantapur.
http://MedicalDeviceEvents.com At the 10x Medical Device Conference in 2014, presenters Carrie Kuehn, Jorge Ochoa, and Robert Packard explained why, according to data from FDA, more than 58% of 510(k) submissions were refused under FDA’s Refuse to Accept (RTA) policy during its first year of implementation.
This presentation examined some of the reasons why industry got such a bad “grade.” We discussed the RTA requirements and some of the challenges from industry’s perspective on meeting the requirements of the RTA checklist and ended with recommendations on how industry can improve its odds of getting past the RTA hurdle on the first try.
Guangzhou Shuokang, founded 10 years ago, is producing laboratory furniture in our factory in Guangzhou. We have a technical staff which has more than 25 years of experience. The factory dedicated to producing laboratory furniture. Shuokang exports 60% of the production to areas outside of Turkey. The world market is asking for high quality products. The products have to be according international and local standards. We produce the furniture according to different standards. We are monitoring the market to check for standards and look for ways to make or keep our furniture according to these standards. Our factory is, of course, accredited according to ISO 9001 Quality System. Our mission is to help you with your laboratory furniture needs. We don’t want to supply you with a set of furniture but with a laboratory solution.Laboratory comprehensive system engineering: Decoration, ventilation, environmental protect, intelligent engineering design and construction,laboratory cabinets,fume hood and other equipment.
FDA Form 483 (Inspectional Observations) - Top Violations 2013Marc Sanchez
FDA Attorney Marc Sanchez discusses the Top FDA Form 483 (Inspectional Observations) from fiscal year 2013. The top observations provide a foundation for preparing for a pre-inspection, for-cause inspection, or routine surveillance inspection.
New PDA/IPEC Technical Report on Excipient Risk Assessment - insights for dru...MilliporeSigma
Access the interactive recording: https://bit.ly/37HqbTK
Abstract:
Since March 2016 the EU Guideline to ascertain the appropriate GMP for pharmaceutical excipients is legally binding. Although the EU Guideline itself provides a high level description how to perform the risk assessment, the implementation can be challenging. In January 2018 PDA and IPEC formed a joint Task Force with the objective to develop a joint Technical Report to share best practices with industry. This Technical Report was published in December 2019. In this webinar you will be introduced to the new Technical Report, its objective, proposed approaches and examples shared by PDA/IPEC member companies.
Global Markets Direct's, 'Esophageal Cancer - Pipeline Review, H1 2013', provides an overview of the indication's therapeutic pipeline. This report provides information on the therapeutic development for Esophageal Cancer, complete with latest updates, and special features on late-stage and discontinued projects.
https://www.reportscorner.com/reports/23243/Esophageal-Cancer-%E2%80%93-Pipeline-Review,-H1-2013/
Ethocle Reports has published its latest Market Research Report on Transdermal Drug Delivery - Medical Devices Pipeline Assessment, 2016. Formulate significant competitor information, analysis, and insights to improve R&D strategies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Transdermal Drug Delivery - Medical Devices Pipeline Assessment, 2016. Identify emerging players with potentially strong product portfolio and create effective counter-strategies to gain competitive advantage. Browse market data tables and figures.
Integra gen s.a (alint) product pipeline analysis, 2014 updateAmbikabasa
Summary IntegraGen S.A (IntegraGen) is a biotechnology service provider. The company provides clinical genomic services to academic researchers and life sciences companies. It offers services such as DNA extraction, management samples, study design, strategy, selection markers, tagging, biostatistics analysis, and bioinformatics analysis of sequence data. IntegraGen provides sequencing and genotyping of DNA and RNA. The company offers services in the fields of pharmacogenetics, cytogenetics, epigenetics, and agriculture. It serves patients, clinicians and researchers. IntegraGen partners with illumia, Fluidigm, DNA genotek and Agitent Certified companies.
http://www.researchmoz.us/integragen-sa-alint-product-pipeline-analysis-2014-update-report.html
Global Markets Direct's, 'Carcinomas - Pipeline Review, H1 2013', provides an overview of the indication's therapeutic pipeline. This report provides information on the therapeutic development for Carcinomas, complete with latest updates, and special features on late-stage and discontinued projects.
https://www.reportscorner.com/reports/23246/Carcinomas-%E2%80%93-Pipeline-Review,-H1-2013/
This report provides comprehensive information on the therapeutic development for Ocular Pain, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type, along with latest updates, and featured news and press releases. It also reviews key players involved in the therapeutic development for Ocular Pain and special features on late-stage and discontinued projects.
http://www.researchmoz.us/ocular-pain-pipeline-review-h1-2015-report.html
This report provides comprehensive information on the therapeutic development for Traveler's Diarrhea, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type, along with latest updates, and featured news and press releases. It also reviews key players involved in the therapeutic development for Traveler's Diarrhea and special features on late-stage and discontinued projects.
http://www.researchmoz.us/travelers-diarrhea-pipeline-review-h1-2015-report.html
Roundup of This Year's AACC Meeting in AtlantaBruce Carlson
The American Association of Clinical Chemistry was held this year in Atlanta, GA. Kalorama was at the meeting and notes several developments, with a particular focus on point-of-care.
This report provides comprehensive information on the current therapeutic developmental pipeline of Genzyme Corporations, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type. It also reviews latest updates, and featured news and press releases, along with special features on late-stage and discontinued projects.
http://www.researchmoz.us/genzyme-corporation-product-pipeline-review-2015-report.html
Non alcoholic steatohepatitis - pipeline review, h1 2014Ambikabasa
This report provides comprehensive information on the therapeutic development for Non-Alcoholic Steatohepatitis, complete with comparative analysis at various stages, therapeutics assessment by drug target, mechanism of action (MoA), route of administration (RoA) and molecule type, along with latest updates, and featured news and press releases. It also reviews key players involved in the therapeutic development for Non-Alcoholic Steatohepatitis and special features on late-stage and discontinued projects.
Ethocle Reports has published its latest Market Research Report on Rx-OTC Switch Opportunities : Trends in OTC, category analysis, case studies and future opportunities. This report takes an in-depth look at the market for Rx-OTC switches. It considers which categories have the most potential for switching, analyzing both past performance and expected future outcomes, and then examines specific candidates. Browse market data tables and figures.
Paper and paperboard global industry guideNelson Permal
Ethocle Reports has published its latest Market Research Report on Paper and Paperboard Global Industry Guide_2016. Essential resource for top-line data and analysis covering the global paper and paperboard market. Includes market size and segmentation data, textual and graphical analysis of market growth trends and leading companies. Browse market data tables and figures.
Otc pharmaceuticals global industry guideNelson Permal
Ethocle Reports has published its latest Market Research Report on OTC Pharmaceuticals Global Industry Guide_2016. Essential resource for top-line data and analysis covering the global otc pharmaceuticals market. Includes market size and segmentation data, textual and graphical analysis of market growth trends and leading companies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on North America Computed Tomography (CT) Systems Market Outlook to 2022. Develop business strategies by identifying the key market segments poised for strong growth in the future. Browse market data tables and figures.
Medical equipment monthly deals analysisNelson Permal
Ethocle Reports has published its latest Market Research Report on Medical Equipment Monthly Deals Analysis: November 2016 - M&A and Investment Trends. Enhance your decision making capability in a more rapid and time sensitive manner. Browse market data tables and figures.
Medical equipment monthly deals analysi1Nelson Permal
Ethocle Reports has published its latest Market Research Report on Medical Equipment Monthly Deals Analysis: November 2016 - M&A and Investment Trends. Enhance your decision making capability in a more rapid and time sensitive manner. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Hyperglycemia - Pipeline Review, H2 2016. Procure strategically important competitor information, analysis, and insights to formulate effective R&D strategies. Browse market data tables and figures.
Healthcare providers global industry guideNelson Permal
Ethocle Reports has published its latest Market Research Report on Healthcare Providers Global Industry Guide_2016. Essential resource for top-line data and analysis covering the global healthcare providers market. Includes market size and segmentation data, textual and graphical analysis of market growth trends and leading companies. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on EpiCast Report: Ulcerative Colitis - Epidemiology Forecast to 2025. Develop business strategies by understanding the trends shaping and driving the global UC market. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on CountryFocus: Healthcare, Regulatory and Reimbursement Landscape – US. Develop business strategies by understanding the trends shaping and driving the US healthcare market. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on CountryFocus: Healthcare, Regulatory and Reimbursement Landscape – US. Develop business strategies by understanding the trends shaping and driving the US healthcare market. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Asia-Pacific Glaucoma Surgery Devices Market Outlook to 2022. Develop business strategies by identifying the key market segments poised for strong growth in the future. Browse market data tables and figures.
Ethocle Reports has published its latest Market Research Report on Anti-hypertensive Therapeutics in Asia-Pacific Markets to 2022. Understand the current clinical and commercial landscape by considering disease pathogenesis, diagnosis, prognosis, and the treatment options available at each stage of diagnosis, including a clinical comparison of marketed therapies. Browse market data tables and figures.
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As an Army veteran dedicated to lifelong learning, I bring a disciplined, strategic mindset to my pursuits. I am constantly expanding my knowledge to innovate and lead effectively. My journey is driven by a commitment to excellence, and to make a meaningful impact in the world.
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Vat Registration is a legal obligation for businesses meeting the threshold requirement, helping companies avoid fines and ramifications. Contact now!
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Building Your Employer Brand with Social MediaLuanWise
Presented at The Global HR Summit, 6th June 2024
In this keynote, Luan Wise will provide invaluable insights to elevate your employer brand on social media platforms including LinkedIn, Facebook, Instagram, X (formerly Twitter) and TikTok. You'll learn how compelling content can authentically showcase your company culture, values, and employee experiences to support your talent acquisition and retention objectives. Additionally, you'll understand the power of employee advocacy to amplify reach and engagement – helping to position your organization as an employer of choice in today's competitive talent landscape.
Recruiting in the Digital Age: A Social Media MasterclassLuanWise
In this masterclass, presented at the Global HR Summit on 5th June 2024, Luan Wise explored the essential features of social media platforms that support talent acquisition, including LinkedIn, Facebook, Instagram, X (formerly Twitter) and TikTok.
[Note: This is a partial preview. To download this presentation, visit:
https://www.oeconsulting.com.sg/training-presentations]
Sustainability has become an increasingly critical topic as the world recognizes the need to protect our planet and its resources for future generations. Sustainability means meeting our current needs without compromising the ability of future generations to meet theirs. It involves long-term planning and consideration of the consequences of our actions. The goal is to create strategies that ensure the long-term viability of People, Planet, and Profit.
Leading companies such as Nike, Toyota, and Siemens are prioritizing sustainable innovation in their business models, setting an example for others to follow. In this Sustainability training presentation, you will learn key concepts, principles, and practices of sustainability applicable across industries. This training aims to create awareness and educate employees, senior executives, consultants, and other key stakeholders, including investors, policymakers, and supply chain partners, on the importance and implementation of sustainability.
LEARNING OBJECTIVES
1. Develop a comprehensive understanding of the fundamental principles and concepts that form the foundation of sustainability within corporate environments.
2. Explore the sustainability implementation model, focusing on effective measures and reporting strategies to track and communicate sustainability efforts.
3. Identify and define best practices and critical success factors essential for achieving sustainability goals within organizations.
CONTENTS
1. Introduction and Key Concepts of Sustainability
2. Principles and Practices of Sustainability
3. Measures and Reporting in Sustainability
4. Sustainability Implementation & Best Practices
To download the complete presentation, visit: https://www.oeconsulting.com.sg/training-presentations
Bài tập - Tiếng anh 11 Global Success UNIT 1 - Bản HS.doc.pdf
Drug eluting stents
1. Drug ElutingStents (DES) - Medical DevicesPipeline Assessment,2016
Ethocle Reportshaspublished its latest MarketResearch Reporton Drug Eluting Stents(DES) - Medical
DevicesPipeline Assessment,2016. Formulatesignificantcompetitorinformation, analysis,and insights
to improveR&D strategies.Browsemarketdata tablesand figures.
PublishedOn:05-Dec-2016 | Pages: 268
Summary
GlobalData'sMedical Devicessectorreport,“DrugElutingStents(DES) - Medical DevicesPipeline
Assessment,2016" providesanoverview of DrugElutingStents(DES) currentlyinpipeline stage.
The report providescomprehensiveinformationonthe pipeline productswithcomparative analysisof
the productsat variousstagesof development.The reportreviewsmajorplayersinvolvedinthe pipeline
productdevelopment.Italsoprovidesinformationaboutclinical trialsinprogress,whichincludestrial
phase,trial status,trial start and enddates,and,the numberof trialsfor the keyDrug ElutingStents
(DES) pipelineproducts.
Thisreportis preparedusingdatasourcedfromin-house databases,secondaryandprimaryresearchby
GlobalData'steamof industry experts.
*Note:Certainsectionsinthe reportmaybe removedoralteredbasedonthe availabilityandrelevance
of data inrelationtothe equipmenttype.
Click here to find out more about this report?
Scope
- Extensive coverage of the DrugElutingStents(DES) underdevelopment
- The report reviewsdetailsof majorpipeline productswhichincludes,productdescription,licensing
and collaborationdetailsandotherdevelopmental activities
2. - The report reviewsthe majorplayersinvolvedinthe developmentof DrugElutingStents(DES) andlist
all theirpipeline projects
- The coverage of pipeline productsbasedonvariousstagesof developmentrangingfromEarly
DevelopmenttoApproved/Issuedstage
- The report provideskeyclinical trial dataof ongoingtrialsspecifictopipeline products
- Recentdevelopmentsinthe segment/industry
Get Free Sample Report
Click here for Discounts
Reasons to buy
The report enablesyouto -
- Formulate significantcompetitorinformation,analysis,andinsightstoimprove R&Dstrategies
- Identifyemergingplayerswithpotentiallystrongproductportfolioandcreate effective counter-
strategiestogaincompetitiveadvantage
- Identifyandunderstandimportantanddiversetypes of DrugElutingStents(DES) underdevelopment
- Developmarket-entryandmarketexpansionstrategies
- Planmergersandacquisitionseffectivelybyidentifyingmajorplayerswiththe mostpromisingpipeline
- In-depthanalysisof the product’scurrentstage of development,territoryandestimatedlaunchdate
Table of Contents
1.1 Listof Tables8
1.2 Listof Figures17
2 Introduction18
2.1 Drug ElutingStents(DES) Overview18
3 ProductsunderDevelopment19
3.1 Drug ElutingStents(DES) - Pipeline ProductsbyStage of Development19
3.2 Drug ElutingStents(DES) - Pipeline ProductsbyTerritory20