Summary - A new market study, titled “Global Power Sports Market (ATV, SSV, Snowmobiles, Motorcycles & PWC): Industry Analysis & Outlook (2017-2021)” has been featured on WiseGuyReports.Power sports vehicles generally have high powered engines and these vehicles are majorly used for recreational and utility purposes.Power sports market is broadly segregated into four major types, having their sub categories as well.Power sports vehicles are classified into off-road vehicles, snowmobiles, personal water crafts and motorcycles.The market is concentrated in developed regions like North America and Europe.Power sports market consists of vehicles which are largely used for leisure and lavish lifestyle.However, the use of power sports vehicles at present is not limited to recreational activities, but it is also being put to use in various construction and military based activities.Also Read: power sports market is driven by strong economic growth, optimistic business outlook, increased motorcycles registration and growing power boats market in particular.
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EligibilityHaving passed the CA Foundation (or CA CPT) exam conducted by ICAI.ORHaving completed their Graduate or Post Graduate Degree in Commerce (with minimum 55% marks/ other graduates with minimum 60% marks).ORHaving passed the Intermediate exam of Institute of Cost Accountants of India or Institute of Company Secretaries of India.Provisional Registration:Students pursuing the final year of Graduation Course shall also be eligible for provisional registration CA Inter by submitting valid proof of having successfully completed graduation with the required marks within six months from the date of appearance in the final year graduation examination.Timeline: 6 Months Passing Criteria40% in each paper and an aggregate of 50% in all papers of Group I.The passing criteria are the same even in cases where the candidate has appeared for each Group separately.In cases where the candidate appears for both Groups together, the candidate is still required to get 40% in each paper and an aggregate of 50% in all 8 papers of Group I and Group II.ExaminationThe examination for the CA Intermediate Course is conducted twice a year; in the months of May and November.NSA Batch for CA IntermediateA candidate may enroll with the NSA at any time of the year.The Course syllabus that a candidate may have missed out on will be taught in the immediate next session.
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यहाँ पर, हमने सेवा और विनिर्माण या उत्पादन इकाई के लिए MSME पंजीकरण की पात्रता के बारे में बताया है।MSME की परिभाषा को केंद्रीय कैबिनेट द्वारा संशोधित और अनुमोदित किया गया था ताकि छोटी व्यापारिक कंपनियों के विकास को बढ़ावा दिया जा सके।MSME की नई परिभाषा को निवेश और कारोबार के आकार के आधार पर फिर से परिभाषित किया गया था।प्रारंभ में, निवेश और वार्षिक कारोबार की मात्रा दोनों के लिए विनिर्माण और सेवा उद्यमों के बीच अंतर था। लेकिन अब दोनों क्षेत्रों में लगे उद्यमों के लिए निवेश और टर्नओवर को समान बनाकर विनिर्माण और सेवा उद्यम के बीच अंतर को समाप्त कर दिया गया है। ने तालिका में MSME के नए वर्गीकरण का उल्लेख किया है। यदि आप MSME पोर्टल में फिर से पंजीकरण करना चाहते हैं, जैसा कि आप जानते हैं कि पंजीकरण प्रक्रिया को यूडियम (UDYAM) पंजीकरण कहा जाएगा, तो कृपया नीचे दिए गए लिंक पर जाएं ।Udyam Registration for Proprietor - प्रोपराइटर के लिए उद्योगम पंजीकरणUdyam Registration for Pvt Limited Company - प्राइवेट लिमिटेड कंपनी के लिए उद्योगम पंजीकरणUdyam Registration for Partnership Firm - साझेदारी फर्म के लिए उद्योग पंजीकरणUdyam Registration for Pubic Limited Company - पब्लिक लिमिटेड कंपनी के लिए उद्योगम पंजीकरणUdyam Registration for Others - दूसरों के लिए उद्योग पंजीकरणलेटेस्ट न्यूज़ और अपडेट के लिए फेसबुक पर हमें फॉलो करें।
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 To order this 330+ page report, please visit this link Key InclusionsA detailed assessment of the current market landscape of targeted protein degradation-based therapeutics, providing information on drug / therapy developer(s) (such as year of establishment, company size and location of headquarters), clinical study sponsor(s) and collaborator(s), type of protein degrader (degronimids, ENDTACs, epichaperome inhibitors, hydrophobic tags, IMiDs, LYTACs, molecular glues, PHOTACs, PROTACs, protein homeostatic modulators, SARDs, SERDs, SNIPERs, and specific BET and DUB inhibitors), phase of development (clinical, preclinical, and discovery stage) of product candidates, target indication(s), key therapeutic area(s), type of target protein(s), target enzyme(s) (if available), target signaling pathway (if available), mechanism of action (if available), type of therapy (monotherapy and combination therapy), route of administration (oral, intravenous and others), and information on special drug designations (if any).In addition, the chapter highlights the various technology platforms that are being actively used for the development of targeted protein degraders.Elaborate profiles of key players that are engaged in the development of targeted protein degraders (shortlisted on the basis of phase of development of pipeline products), featuring a brief overview of the company, its financial information (if available), detailed descriptions of their respective lead drug candidates, and an informed future outlook.Additionally, each drug profile features information on the type of drug, route of administration, target indications, current status of development and a brief summary of its developmental history.Brief tabulated profiles of industry players (shortlisted on the basis of the number of pipeline products), featuring details on the innovator company (such as year of establishment, location of headquarters, number of employees, and key members of the executive team), recent developments, along with descriptions of their respective drug candidates.A detailed clinical trial analysis of completed, ongoing and planned studies of various targeted protein degraders, highlighting prevalent trends across various relevant parameters, such as current trial status, trial registration year, enrolled patient population and regional distribution of trials, type of protein degrader, phase of development, study design, leading industry and non-industry players (in terms of number of trials conducted), study focus, target therapeutic area, key indications, and clinical endpoints.An assessment of the relative experience of key opinion leaders (KOLs) within this domain, (shortlisted based on their involvement in various clinical studies), featuring detailed 2X2 matrices (based on the strength and activeness of KOLs), a schematic world map representation (highlighting the geographical locations of eminent scientists / researchers) and an analysis evaluating the (relative) level of expertise of different KOLs, based on parameters such as number of publications, number of citations, participation in clinical trials, number of affiliations and strength of professional network (based on information available on ResearchGate).A detailed publication analysis of more than 210 peer-reviewed, scientific articles that have been published since 2017, highlighting the research focus within the industry.It also highlights the key trends observed across the publications, including information on novel protein degraders, potential target proteins, target disease indications, and analysis based on various relevant parameters, such as year of publication, and most popular journals (in terms of number of articles published in the given time period) within this domain.An analysis of the partnerships that have been established in the domain, over the period 2014-Q3 2019, covering research agreements, product / technology licensing agreements, mergers / acquisitions, asset purchase agreements, R and commercialization agreements, IP licensing agreements, clinical trial agreements, product development agreements, and other relevant deals.An analysis of the investments made at various stages of development, such as seed financing, venture capital financing, debt financing, grants / awards, capital raised from IPOs and subsequent offerings, by companies that are engaged in this field.The report also features the likely distribution of the current and forecasted opportunity across important market segments, mentioned below:Type of payment of licensing agreementsUpfront paymentsMilestone payments Type of protein degraderDegronimidsPROTACsSARDs / SERDsSpecific BET and DUB inhibitorsOther protein degraders Therapeutic areaNeurodegenerative disordersOncological disordersOther therapeutic areas Route of administrationOralIntravenousOther routes Key geographical regionNorth AmericaEuropeAsia-Pacific To request a sample pages, please visit this link Key Questions AnsweredWhat are the prevalent R trends related to targeted protein degradation?Which clinical conditions can be treated using targeted protein degradation-based therapeutics?What are the most popular proteins being targeted by bifunctional degrader molecules?What are the key challenges faced by stakeholders engaged in this domain?What are the key technology platforms that leverage the concept of targeted protein degradation?Who are the leading industry and non-industry players in this market?What are the contributions of big pharma players in this field?What are the key geographies where research on targeted protein degradation is being conducted?Who are the key investors in this domain?Who are the key opinion leaders / experts in this field?What kind of partnership models are commonly adopted by industry stakeholders?What are the factors that are likely to influence the evolution of this upcoming market?How is the current and future market opportunity likely to be distributed across key market segments?You may also be interested in the following titles:DNA-Encoded Libraries: Platforms and Services MarketGlobal Stem Cells Market: Focus on Clinical Therapies, 2020–2030The Human Microbiome Market: Focus on Therapeutics (including gut-brain axis targeting drugs), Diagnostics and Fecal Microbiota Therapies (3rd Edition), 2019-2030  Contact Details:Gaurav Chaudhary+1 (415) 800 [email protected] 
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Summary - A new market study, titled “Global Event Management Software Market by Manufacturers, Regions, Type and Application, Forecast to 2023 ” has been featured on WiseGuyReports.Geographically, this report is segmented into several key Regions, with production, consumption, revenue (M USD), market share and growth rate of Event Management Software in these regions, from 2012 to 2023 (forecast), covering North America (United States, Canada and Mexico) Europe (Germany, France, UK, Russia and Italy) Asia-Pacific (China, Japan, Korea, India and Southeast Asia) South America (Brazil, Argentina, Columbia)ALSO READ: East and Africa (Saudi Arabia, UAE, Egypt, Nigeria and South Africa) Global Event Management Software market competition by top manufacturers, with production, price, revenue (value) and market share for each manufacturer; the top players including Cvent Active Network Xing Events Etouches Eventbrite Ungerboeck Software International Dean Evans and Associates Certain Lanyon Solutions Zerista On the basis of product, this report displays the production, revenue, price, market share and growth rate of each type, primarily split into Venue management software Event registration software Ticketing software Event planning software Event marketing software Analytics software ????Others?On the basis on the end users/applications, this report focuses on the status and outlook for major applications/end users, consumption (sales), market share and growth rate of Event Management Software for each application, including Corporate Education Government Third-party planners OthersIf you have any special requirements, please let us know and we will offer you the report as you want.FOR MORE DETAILS: Us:Wise Guy Reports is part of the Wise Guy Research Consultants Pvt.Ltd. and offers premium progressive statistical surveying, market research reports, analysis & forecast data for industries and governments around the globe.Contact Us:NORAH TRENT                                                      [email protected]       Ph: +162-825-80070 (US)                          Ph: +44 203 500 2763 (UK)        
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Several approved therapeutic products, which are currently available as intravenous dosage forms, are being reformulated and evaluated for subcutaneous administration.Further, many existing drug delivery devices, including prefilled syringes, pen injectors, autoinjectors, needle-free injectors and large volume wearable injectors, have been / are being designed for subcutaneous administration of biologics.To order this 530+ page report, which features 160+ figures and 190+ tables, please visit this link The USD 180+ billion (by 2030) financial opportunity associated with subcutaneous biologics, affiliated drug delivery systems and subcutaneous formulation technology licensing deals, has been analyzed across the following segments:Phase of developmentApprovedPre-registration & Phase IIIPhase II & Phase II/III Type of moleculeCell and gene therapiesMonoclonal antibodiesProteinsPeptides (recombinant)VaccinesOthers Target therapeutic areaAutoimmune disordersBlood disordersBone disordersGenetic disordersMetabolic disordersNeurological disordersOncological disordersRespiratory disordersOthers Type of drug delivery systemLarge volume wearable injectorsAutoinjectorsPrefilled syringesNeedle-free injectorsDrug reconstitution systems Revenues from licensing dealsUpfront paymentsMilestone payments Key geographical regionsNorth AmericaEuropeAsia PacificRest of the World The Subcutaneous Biologics, Technologies and Drug Delivery Systems (3rd Edition), 2020-2030 report features the following companies, which we identified to be key players in this domain:AdociaAjinomoto Bio-Pharma ServicesArecorAlteogenAscendis PharmaAvadel PharmaceuticalsCamurusCreative BioMartCreative BiolabsDURECTEagle PharmaceuticalsHalozyme TherapeuticsMedinCellXeris PharmaceuticalsSerina Therapeutics Table of ContentsPreface Executive Summary Introduction Subcutaneous Biologics: Current Market Landscape Case Study: Leading Subcutaneous Biologics Subcutaneous Formulation Technologies: Current Market Landscape Subcutaneous Formulation Technology Developers: Company Competitiveness Analysis Subcutaneous Formulation Technology Developers: Company Profiles Partnerships and Collaborations Subcutaneous Drug Delivery Systems: Current Market Landscape Swot Analysis Market Forecast and Opportunity Analysis Concluding Remarks Executive Insights Appendix 1: Tabulated Data  Appendix 2: List Of Companies And Organization  To purchase a copy, please visit Contact DetailsGaurav Chaudhary+1 (415) 800 3415+44 (122) 391 [email protected] 
Subcutaneous drug delivery, given the use of tailored formulation development solutions, has brought about a paradigm shift in at-home healthcare, enabling users to administer (life-saving) medications without having to rely on medical professionals Roots Analysis is pleased to announce the publication of its recent study, titled “Subcutaneous Biologics, Technologies and Drug Delivery Systems (3rd Edition), 2020-2030” report to its list of offerings.The report provides a detailed study on the current market landscape and future potential of biologics designed for subcutaneous administration.In addition, the study provides an in-depth analysis of the formulation technologies and drug delivery systems (focusing on large volume wearable injectors, autoinjectors, pen injectors, needle-free injectors, drug reconstitution systems, prefilled syringes and implants) that enable subcutaneous delivery of the biologic drugs.Amongst other elements, the report features the following:A detailed assessment of the current market landscape of commercially available and clinical-stage biologics that are designed for delivery via the subcutaneous routeA case study on leading subcutaneous biologics (in terms of revenues generated), featuring details on mechanism of action, development history, annual sales, technology platform (if available), and a comparison of their intravenous and subcutaneous formulations (if applicable).An assessment of the various subcutaneous formulation technologies along with information on developers, type of pharmacological molecule, route of administration, mechanisms of action and primary advantage(s).An insightful three-dimensional comparison of the subcutaneous formulation technology developers, based on pipeline strength, supplier power of the developer and primary advantages offered by their respective technologies.Elaborate profiles of key technology developers, featuring a brief overview of the company, its technology portfolio, product portfolio, financial information (if available), recent developments and an informed future outlook.An analysis of collaborations and partnership agreements inked by the subcutaneous formulation technology developers since 2011An in-depth review of the most advanced and popular subcutaneous drug delivery systems, including large volume wearable injectors, autoinjectors, pen injectors, needle-free injectors, drug reconstitution systems, prefilled syringes and implantsA comprehensive product competitiveness analysis of subcutaneous large volume wearable injectors, subcutaneous autoinjectors, subcutaneous needle-free injectors and pre-filled syringesA discussion on affiliated trends, key drivers and challenges, which are likely to impact the industry's evolution, under a comprehensive SWOT frameworkA detailed market forecast, featuring analysis of the current and projected future opportunity across key market segments (listed below):Phase of developmentApprovedPre-registration & Phase IIIPhase II & Phase II/III Type of moleculeCell and gene therapiesMonoclonal antibodiesProteinsPeptides (recombinant)VaccinesOthers Target therapeutic areaAutoimmune disordersBlood disordersBone disordersGenetic disordersMetabolic disordersNeurological disordersOncological disordersRespiratory disordersOthers Type of drug delivery systemLarge volume wearable injectorsAutoinjectorsPrefilled syringesNeedle-free injectorsDrug reconstitution systems Revenues from licensing dealsUpfront paymentsMilestone payments Key geographical regionsNorth AmericaEuropeAsia PacificRest of the World Transcripts of interviews held with the following senior level representatives of stakeholder companiesDeborah Bitterfield (Founder and Chief Executive Officer, Lindy Biosciences)Matthew Young (Founder and Chief Technology Officer, Oval Medical Technologies)Steve Prestrelski (Founder and Chief Scientific Officer, Xeris Pharmaceuticals), Hong Qi (Vice President, Product Development, Xeris Pharmaceuticals) and Scott Coleman (Senior Scientist, Formulation, Xeris Pharmaceuticals)David Daily (Co-Founder and Chief Executive Officer, DALI Medical Devices)Michael Reilly (Co-Founder and Chief Executive Officer and Co-Founder, Excelse Bio)Poonam R Velagaleti (Co-Founder, i-novion)Michael Hooven (Chief Executive Officer, Enable Injections)Frederic Ors (Chief Executive Officer, Immunovaccine Technologies)Patrick Anquetil (Chief Executive Officer, Portal Instruments)Menachem Zucker (Vice President and Chief Scientist, Elcam Medical)Tiffany H. Burke (Director, Global Communications, West Pharmaceutical Services) and Graham Reynolds (Vice President and General Manager, Global Biologics, West Pharmaceutical Services)David Heuzé (Communication Leader, MedinCell) Key companies covered in the reportAdociaAjinomoto Bio-Pharma ServicesArecorAlteogenAscendis PharmaAvadel PharmaceuticalsCamurusCreative BioMartCreative BiolabsDURECTEagle PharmaceuticalsHalozyme TherapeuticsMedinCellXeris PharmaceuticalsSerina Therapeutics For additional details, please visit Other Recent OfferingsGlobal Autoinjectors Market (3rd Edition), 2020-2030Prefilled Syringes Market (5th Edition), 2020-2030Microneedles and Needle-Free Injection Systems / Jet Injectors (Devices based on Spring, Gas and Other Mechanisms) Market, 2019-2030Large Volume Wearable Injectors Market (4th Edition), 2018-2030  About Roots AnalysisRoots Analysis is one of the fastest growing market research companies, sharing fresh and independent perspectives in the bio-pharmaceutical industry.The in-depth research, analysis and insights are driven by an experienced leadership team which has gained many years of significant experience in this sector.If you’d like help with your growing business needs, get in touch at [email protected] Contact InformationRoots Analysis Private LimitedGaurav Chaudhary+1 (415) 800 [email protected]  
MSME Classification Registration EligibilityThis is the latest revised MSME classification and registration eligibility for micro small-medium scale industry.Micro Enterprise:: MSMEs will now be called a Microenterprise where the investment does not exceed Rs 1 crore rupees and the Turnover does not exceed Rs 5 crore rupees.Small Enterprise:: Small Enterprise where its investment in plant and machinery limit has been raised from Rs 5 crore to Rs 10 crore with a turnover of less than 50 crores.Medium Enterprise:: With investments up to Rs 50 crore with a turnover of less than Rs 250 crore comes under Medium Enterprise.Earlier, the investment limit for Medium enterprise was up to Rs 10 crore and Service enterprises up to Rs 5 crore.EnterpriseTurnoverInvestmentMicroNot more than 5 Cr.Not more than 1 Cr.SmallNot more than 50 Cr.Not more than 10 Cr.MediumNot more than 250 Cr.Not more than 50 makes the online process for MSME registration very simple and user-friendly.The online registration process of MSME is simple for any business individual as follows:Step 1: Visit the MSME Registration portalStep 2: Fill all the details on MSME Registration Form, like aadhaar number, name, and addressStep 3: Make the online payment for your MSME Registration ApplicationStep 4: One of our registration experts will process your MSME Registration applicationStep 5: In 1-2 hours you will receive your MSME Registration e-certificate at your registered e-mail address.Above we have mentioned various benefits of getting an MSME registration certificate for your business.If you any doubt about the eligibility of MSME registration then contact us.