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How to Export Medicines from India: A Comprehensive Guide
India stands as a prominent global player in the pharmaceutical industry, known for its extensive production and export of medicines. With its substantial contribution to the world's pharmaceutical needs, understanding how to export medicines from India can be both lucrative and impactful. This article provides a detailed overview of the process, requirements, and key insights into medicine exports from India.
1. Overview of India's Pharmaceutical Export Market
India is a major force in the global pharmaceutical market, contributing significantly to the production and supply of medicines. Here’s a snapshot of India’s pharmaceutical export landscape:
Global Leadership: India accounts for 20% of the world’s pharmaceutical volume and over 60% of global vaccine supply.
Export Growth: Pharmaceutical exports from India surged from Rs. 90,415 crore in 2013–14 to Rs. 2,04,110 crore in 2022–23, reflecting a remarkable growth trajectory.
Key Products: The primary products exported include formulations, biologics, bulk pharmaceuticals, and drug intermediates. Formulations and biologics alone make up approximately 73.31% of India’s pharmaceutical exports.
2. Major Medicines Exported from India
India’s pharmaceutical sector exports a wide range of medicines. Some of the most commonly exported medicines include:
Analgesics & Anti-Inflammatories
Antispasmodic Analgesics
Diuretics & Anti-Diuretics
Pro-Kinetics & Gut Relaxants
Anti-Asthmatics
Antibacterials
These medicines are essential in various therapeutic areas, including pain management, gastrointestinal health, respiratory issues, and bacterial infections.
3. Key Destinations for Indian Medicines
India’s pharmaceutical exports reach over 200 countries, with significant markets including:
United States: The largest importer, accounting for over 31% of India’s pharmaceutical exports.
South Africa
Belgium
United Kingdom
Brazil
India’s export markets also extend to the Middle East, Asia, CIS, North America, Africa, the European Union, ASEAN, Latin America, and the Caribbean.
4. Steps to Export Medicines from India
Exporting medicines from India involves several crucial steps:
Business Registration and Documentation:
Register Your Business: Ensure your business is registered with the Ministry of Corporate Affairs (MCA) and has GST registration.
Obtain an Import Export Code (IEC): Required for international trade.
Drug License: A license from the relevant Drug Regulatory Authority in India.
Certificate of Pharmaceutical Product (CPP): Required for international markets.
Product Compliance:
Get Approval from DCGI: Ensure your products meet the Drug Controller General of India’s standards.
Product Registration in Destination Country: Comply with the regulatory requirements of the importing country.
Logistics and Distribution:
Customs Clearance: Work with a customs agent to manage export documentation and compliance.
Find Distributors and Buyers: Establish connections with international distributors or buyers.
Export Documentation:
Certificate of Analysis
Letter of Credit (if applicable)
Proforma Invoice
Destination Control Statement
5. Key Export Data and Trends
2021–2022: India’s pharmaceutical exports amounted to US$ 24.62 billion, with a 1% increase from the previous year.
2022–2023: The total value of pharmaceutical exports reached US$ 25.4 billion.
Growth Rate: The export value grew by 18% year-on-year from 2020–21 to 2021–2022.
Formulations and biologics dominated the export market, representing about 75% of total pharmaceutical exports.
6. Leading Pharmaceutical Exporters in India
Some of the prominent medicine exporters in India include:
Elkos Healthcare Pvt. Ltd.
Aurobindo Pharma
Cipla Limited
Dr. Reddy’s Laboratories
Sun Pharmaceutical Industries
Lupin Limited
These companies have established themselves as significant contributors to the global pharmaceutical supply chain.
7. Why is India Famous for Medicine?
India’s prominence in the pharmaceutical industry is attributed to:
Affordable and High-Quality Medications: India is often referred to as the "Pharmacy of the World" due to its ability to produce cost-effective medicines.
Medical Tourism: India is a leading destination for medical tourism, offering advanced medical care at lower costs compared to many Western countries.
Rich Heritage in Ayurveda: India’s traditional medical system, Ayurveda, continues to be a significant aspect of its pharmaceutical offerings, particularly in the export of herbal and traditional medicines.
8. Conclusion
Exporting medicines from India involves a structured process, including obtaining the necessary licenses, complying with international regulations, and navigating logistics. With its strong position in the global pharmaceutical market, India offers substantial opportunities for businesses in the medicine export sector. By understanding the market dynamics and adhering to the required steps, businesses can successfully engage in pharmaceutical exports.
For detailed and up-to-date export data and to connect with medicine exporters, platforms like Eximpedia.app provide valuable insights and resources.
FAQs
Who is the largest exporter of medicine in India?
Elkos Healthcare Pvt. Ltd. is considered the largest exporter, alongside other significant players like Aurobindo Pharma and Cipla Limited.
What medicines are exported from India?
Major exports include analgesics, anti-inflammatories, diuretics, and antibacterials.
How to start pharma export?
Understand market dynamics, obtain necessary documentation, and comply with regulatory requirements.
Which countries buy medicine from India?
Major importers include the United States, South Africa, Belgium, the UK, and Brazil.
How many documents are required for pharma export?
Required documents include business registration, drug license, IEC, CPP, and more.
Why is India famous for medicine?
India is known for its affordable medications, rich Ayurvedic heritage, and robust pharmaceutical sector.
For more information on Ayurvedic medicine export from India or other related queries, contact Eximpedia.app for the latest global trade data and insights.
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Beyond Diagnosis: Exploring Global Adrenogenital Syndrome Treatment Market
The global adrenogenital syndrome treatment market will rise at a constant compound annual growth rate (CAGR) of 5.6% from 2023 to 2033, arriving at US$12.81 billion in 2023. The growing focus on innovative therapy techniques that improve patient outcomes is the cause of this expansion.
The adrenal glands are impacted by the genetic disorder known as AGS, which causes hormonal irregularities. Reducing symptoms and controlling these imbalances are the objectives of treatment.
Newborn screening programs in Austria are intended to detect severe cases of AGS so that the affected children can receive the necessary treatment to avert potentially fatal crises involving salt-wasting. Swap therapy is one of the therapies provided as part of newborn screening programs. Lesser variations, sometimes referred to as non-classical AGS, cause symptoms that may go undiagnosed for a long time since they appear later in life and are milder than those of classical AGS.
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It is anticipated that surgical correction of aberrant genital looks will further boost the market. The hormones that the adrenal glands are unable to produce are also replaced by hormonal therapy. Patients with long-term atopic illnesses are prescribed hydrocortisone or corticosteroids on a regular basis. The course of this medication is expected to normalize testosterone production.
Market Competition:
Strategic partnerships can boost revenue and market share for manufacturers by increasing production and meeting consumer demands. To ensure that end users are able to benefit from the use of new products and technologies, you must promote them to end users. By forming a strategic partnership, a company can increase the amount of production it can do as a result of an increase in its capacity.
Spruce Biosciences Inc. and Kaken Pharmaceutical Co. Ltd announced a licensing agreement to develop and commercialize Spruce’s product candidate, tildacerfont, for treating congenital adrenal hyperplasia (CAH). Spruce will receive a $15 million upfront payment from Kaken as part of the agreement, and additional payments are pending upon reaching future development and commercial milestones. In addition to that, tiers of double-digit royalties will be paid on Japanese net sales. For all other geographies, Spruce will retain all rights to tildacerfont, while Kaken will develop and market it in Japan.
A new Phase 2 study from Neurorocrine Biosciences, Inc. is being presented demonstrating substantial reductions in adrenal androgens and androgen precursors in adolescent patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency (21-OHD). As part of its presentation in Hall A1, the company also provided information regarding patient preferences and treatment patterns for classic CAH.
Key Companies Profiled:
Crystal Pharma
Monarch Pharmaceuticals, Inc.
Jubilant Cadista Pharmaceuticals Inc.
Pfizer CentreOne
Healthkey Lifescience Pvt. Ltd.
Zydus Pharmaceuticals
Praxgen Pharmaceuticals
Sandoz
Vintage Labs
Actavis, Inc.
Key Segments Profiled in the Adrenogenital Syndrome Treatment Market Industry Survey:
By Drug Type:
Mineralocorticoids
Glucocorticoids
By Route of Administration:
Oral
Parenteral
Intravenous
Inhaled
Others
By Distribution Channel:
Hospital Pharmacies
Retail Pharmacies
Others
By Region:
North America
Latin America
Europe
Asia Pacific
Middle East & Africa
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Malaria Treatment Market to nearly reach US$ 3 Billion by 2033; expected to surge at a 5% CAGR | FMI Report
In 2023, the Malaria Treatment Market is projected to be valued at US$ 1.80 billion, up from US$ 1.72 Billion in the fiscal year 2022. The market is anticipated to increase at a 5% CAGR from 2023 to 2033, reaching US$ 2.93 billion by the end of that year.
According to the Globe Intellectual Property Organization (WIPO), more than 210 million people were affected by malaria in the world in 2019. Malaria is a contagious, sometimes lethal disease. It is caused by Plasmodium, a little parasite that mosquitoes transmit to humans. Malaria may be caused by four different plasmodium species; however, plasmodium falciparum is the one that most often results in fatal cases.
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Due to increased funding from regional governments, the global market for anti-malaria drugs is likewise growing rapidly. This money ought to make it feasible for research companies like Medicines for Malaria Venture to keep looking at potential lead chemicals that might combat malaria. For instance, in November 2017, the US Agency for International Development (USAID) gave US$ 9 million to Medicines for Malaria Venture to be used for three projects: a pharmacovigilance study of Pyramax (pyronaridine-artesunate), a SERC Phase III research to establish a single-exposure revolutionary cure, and a study to evaluate the efficacy of DSM265, a prospective single-exposure radical cure. These improvements are anticipated to drive the global market for malaria therapy.
Region-wise, the MEA will grow with the fastest CAGR during the forecast period. The Middle East and Africa have held the lion's share of the market share and are expected to continue doing so in the future due to the fast rising incidence of malaria in the region. According to the World Health Organization (WHO) report 2021, 241 million cases of malaria were anticipated worldwide in 2020, with 228 million of those cases happening in the WHO African Region. As a result, one of the largest segments of the market for anti-malarial medications is expected to come from the Middle East and Africa. Such developments will bolster the growth from 2023-2033.
Key Takeaways from the Market Study
The global malaria treatment market is currently worth more than US$ 1.72 Billion.
The oral segment by route of administration is going to occupy a 49% global market share in 2023.
The hospital pharmacies segment by distribution channel type will be the fastest growing segment during the forecast period with a 5.4% CAGR.
The North American region is predicted to grow with a steady CAGR of 4.6% during 2023-2033.
The MEA malaria treatment market is expected to grow with a steady CAGR of 5.5% during 2023-2033.
“Some of the factors driving the market for malaria therapy include the incidence of malarial infection, government initiatives and awareness-raising campaigns, the availability of anti-malarial drugs, and rising healthcare expenditures.” comments a Future Market Insights analyst.
Competitive Landscape
Zydus Healthcare Ltd., Sun Pharmaceutical Industries Ltd., Sanofi SA, GSK Plc, Novartis AG, Cipla Ltd, Viatris Inc., Lupin Ltd, Advacare Pharma USA Llc, and VLP Therapeutics LLC are a few of the well-known companies in the worldwide market for treating malaria.
The Gates Foundation-funded Gavi immunization programme introduced the GlaxoSmithKline (GSK) Mosquirix vaccine in three African countries—Kenya, Ghana, and Malawi—in July 2022. The first antimalarial vaccine ever created is allegedly this one. In countries with moderate to high P. falciparum malaria transmission rates, this is an essential initial step in the malaria vaccine deployment.
In March 2022, Tafenoquine, a brand-new drug that cures a particular strain of malaria, received a license in Australia from Medicines for Malaria Venture (MMV), which also co-developed the drug with GlaxoSmithKline (GSK) for use in children and teenagers. The drug is coupled with chloroquine, a popular anti-malarial drug.
Key Segments Covered in the Malaria Treatment Market Report
Malaria Treatment Market by Treatment:
Prescription Medications
Vaccines
Diagnostic Tests
Others
Malaria Treatment Market by Drug Type:
Branded
Generic
Malaria Treatment Market by Route of Administration:
Oral and Parenteral
Intravenous
Malaria Treatment Market by Distribution Channel:
Direct Tender
Hospital Pharmacies
Retail Pharmacies
Online Pharmacies
Others
Malaria Treatment Market by End User:
Hospitals
Specialty Clinics
Homecare
Others
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Biosimulation Market Current and Future Trends, Leading Players, Industry Segments and Regional Forecast to 2023 to 2032 | Says FMI
The Global Biosimulation Market according to a recent market study by Future Market Insights, was valued at US$ 2.6 billion in 2021 and is predicted to grow to US$ 20.9 billion by 2032. According to the report’s conclusions, biosimulation software will continue to be crucial for the market because it will account for the majority of sales. Software biosimulation will give the trials better and more effective findings, and there are many different types of software accessible for different types of research and application. From 2015 through 2021, the software segment’s revenue increased at a CAGR of 14.3%.
Revenue through Drug Development to Continue being growth Axis For Biosimulation Market
Pharmaceutical companies use biosimulation for drug development. During a drug, development process biosimulation helps to identify the possible effects that the drug can have on a patient. The market through the drug development segment recorded a CAGR of 16.3% during 2015-2021.
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Biosimulation Market: Competition Insights
The key companies operating in the biosimulation market include Certara, Dassault Systemes, Advanced Chemistry Development, Simulation Plus Inc., Schrodinger, Inc., Chemical Computing Group, Physiomics Plc, Rosa & Co. LLC, BioSimulation Consulting Inc., Genedata AG, Instem Group of Companies, PPD, Inc., Insilico Biotechnology AG, Rhenovia Pharma, LeadInvent Technologies, Nuventra Pharma, and In Silico Biosciences.
Some of the recent developments by key providers of biosimulation are as follows:
In June 2022, Certara announced its new version of Biosimulation software for the progress of Novel Biologics. The new version includes Immunogenicity (IG), Immuno-Oncology (IO), and Vaccine simulators to understand and predict how drugs work and point out the key questions in the development of novel biologic therapies.
In June 2022, Genedata AG announced that Syros Pharmaceuticals has chosen Genedata AG’s Genedata Profiler as its data integration and investigative platform to accelerate its translational research strategy.
In March 2022, Advanced Chemistry labs announced that Pharmaron Inc. has chosen its NMR processing and interpretation software.
In March 2022, Simulation Plus, Inc. released its Membrane Plus 3.0 software. The new software includes improved data handling and simulation performance for in vitro-in vivo for extrapolation (IVIVE) for permeability, skin penetration, and release assay systems.
In February 2022, the US Food and Drug Administration (FDA) approved the license for Certara’s Immunogenicity (IG) stimulator to research and assess immunogenicity in protein-based remedies.
In February 2022, Physiomics Plc updated a new agreement with ValiRx plc. According to the new agreement, ValiRx will be able to use Physiomics Plc’s latest version of its Virtual Tumour technology. Physiomics Plc will also help ValiRx in modeling the use of VAL201 peptide in endometriosis (VAL301) and Coronavirus (BC201).
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More Insights Available
Future Market Insights, in its new offering, presents an unbiased analysis of the Biosimulation Market, presenting historical market data (2017-2021) and forecast statistics for the period of 2022-2032.
The study reveals essential insights by Product Type (Services (In-house services, Contract services), Software), by Deployment mode (Drug Development, Drug Discovery, Other Applications), by End-use (Pharmaceutical & Biotechnology Companies, CROs, Regulatory Authorities, Academic Research Institutions), across five regions (North America, Latin America, Europe, Asia Pacific, and Middle East & Africa).
Key Segments Covered in Biosimulation Industry Survey
Biosimulation Market by Product Type:
Services
In-house services
Contract services
Software
Biosimulation Market by Deployment Mode:
Drug Development
Drug Discovery
Other Applications
Biosimulation Market by End-use:
Pharmaceutical &Biotechnology Companies
CROs
Regulatory Authorities
Academic Research Instituitons
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Find the best pharmaceutical distributor in Gulf and MENA region, who provide a wide range of digital advertising services for pharma companies, that help you help in licensing & provide a distributors network to sell your products.
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Pharmaceutical Progression and the dicyclohexylcarbodiimide
Pharmaceutical Progression and the dicyclohexylcarbodiimide
Dicyclohexylcarbodiimide is the primary medication used in the treatment of Crohn's disease and is a licensed drug in Australia. The Global "Dicyclo Hexane (DHC) Market Report provides an in depth market analysis by highlighting important data on various factors surrounding global drivers, challenges, opportunities, threats and economies including key areas of growth, key drivers, therapeutic regions, market size, therapeutic classification, geographic expansion and competition. This report is an authoritative statistical analysis of the global Dicyclo Hexane (DCMDi) industry providing data to create strategies for future growth and success.
This report focuses on the Mexico region providing an in depth look at the pharmaceuticals, generic manufacturers, distributors, medical device companies and suppliers. Data is presented in this document in the Mexico region. This Mexico region Mexico launched the dicyclohexylcarbodiimide which treats Crohn's disease.
This Mexico Review provides an in depth analysis and key factors surrounding dicyclohexylcarbodiimide. Mexico is one of the key players in the global marketplace. Mexico has an impressive pharmaceutical portfolio with many new agents being introduced. This includes an extensive range of topical medicines, intravenous medications, inhalation medications, injectable medications and oral medicines.
Dicyclohexylcarbodiimide belongs to the carbodiimides which are formed naturally by bacteria. The scientific name for carbodiimides is Carbocysteine. This ingredient is used to treat a wide variety of diseases such as arthritis, psoriasis and skin diseases. Dicyclohexylcarbodiimide market research has its main components, namely, L-Cysteine, L-Glutamic Acid, N-acetyl Cysteine, N-ethylenediamine, N-aminoethanolamine and N-acetyl-dihydrotestosterone or HET. dicyclohexylcarbodiimide is introduced into the body through inhalation, injection and tablet forms. dicyclohexylcarbodiimide has low to moderate severity of side effects and hence is used as a systemic replacement therapy in many conditions.
dicyclohexylcarbodiimide has a major marketing channel in Australia, USA and Canada. The major distributors are GlaxoSmithKline, Genzyme, Teva, Meridia, Actonel, Dymatize and Cellex. dicyclohexylcarbodiimide is formulated in clinical trials as a prescription drug. dicyclohexylcarbodiimide is made available in tablet, capsule, powder and injection forms. dicyclohexylcarbodiimide sales in Australia are reported at $4.4 million and it is expected to achieve $7 million in the year 2021.
The report covers Australia's national pharmaceutical market size and trends. It first examines trends in the past two years where dicyclohexylcarbodiimide sales increased by 66% and there were no new generic applications filed. The second year was less profitable with sales down 11%. The third consecutive year sales growth was up to 8%.
The report offers in-depth analysis for the four major regions of Australia (Tasmania, South Australia, Victoria and Queensland) and the states of New South Wales, Victoria, Queensland, Western Australia and South Australia. It provides regional comparisons for overall sales volume and the percentages of prescriptions delivered in each region. It further analyzes the key drivers and key issues for each region. The report includes key performance indicators and a performance rating system. It provides data on the key issues influencing the volume of prescriptions in each region and lists the recommendations made on improving the performance.
The clinical practice has identified three important drivers of dicyclohexylcarbodiimide demand, affordability, convenience and the quality of the drug. In addition to identifying the key players, the market size is also explored. The market size is derived from data on the number of treatments prescribed and the number of patients per treatment prescribed. The data is analyzed by using a dynamic process that addresses the changing size of the markets over time and the drivers behind this. The process identifies the key players and the regulatory environment to identify opportunities that can be exploited to further enhance the sale of dicyclohexylcarbodiimide. | jincheng | highfine biotech | market segment analysis} A second analysis is performed on the pharmaceutical properties of the drug, particularly the efficacy and the safety profile. The clinical study includes two additional steps. The first step analyzes the toxicity profile in mice and rats. This was done using high quality standards to assess for any negative effects. The second step uses sensitivity analysis to evaluate the safety of the drug in autistic children.
The third step of the dicyclohexylcarbodiimide clinical development program assesses the clinical study criteria and design used. This includes an analysis of the protocols, regulatory submission, clinical study protocol requirements and the management plan review and approval. The final step of the evaluation includes a sensitivity analysis of the dicyclohexylcarbodiimide, marketing program and pricing strategy.
The four steps involved in this procedure include (a) statistical calculation of the revenue from the various factors; (b) identification of the price targets and milestones; (c) identification of the revenue source and its profitability; and (d) preparation of a marketing plan by considering the data and the forecasts from all these four factors. The dicyclohexylcarbodiimide has been approved by the FDA and is undergoing the facilities for the manufacture of the capsules. It is anticipated that the launch of the capsules will be during the first half of 2021. The marketing program involves various factors to increase the sales of the medication throughout the various regions.
The research team projects that the Dicyclohexylcarbodiimide (DCC) market size will grow from XXX in 2020 to XXX by 2027, at an estimated CAGR of XX. The base year considered for the study is 2020, and the market size is projected from 2020 to 2027.
The prime objective of this report is to help the user understand the market in terms of its definition, segmentation, market potential, influential trends, and the challenges that the market is facing with 10 major regions and 50 major countries. Deep researches and analysis were done during the preparation of the report. The readers will find this report very helpful in understanding the market in depth. The data and the information regarding the market are taken from reliable sources such as websites, annual reports of the companies, journals, and others and were checked and validated by the industry experts. The facts and data are represented in the report using diagrams, graphs, pie charts, and other pictorial representations. This enhances the visual representation and also helps in understanding the facts much better.
By Market Players: Maokang Biotech Carl Roth Jincheng Pharma Biosynth Carbosynth Guansheng Chemical Huihai Pharma Highfine Biotech
By Type Purity<99% Purity≥99%
By Application Activator Dehydrating Agent Others
By Regions/Countries: North America United States Canada Mexico
East Asia China Japan South Korea
Europe Germany United Kingdom France Italy Russia Spain Netherlands Switzerland Poland
South Asia India Pakistan Bangladesh
Southeast Asia Indonesia Thailand Singapore Malaysia Philippines Vietnam Myanmar
Middle East Turkey Saudi Arabia Iran United Arab Emirates Israel Iraq Qatar Kuwait Oman
Africa Nigeria South Africa Egypt Algeria Morocoo
Oceania Australia New Zealand
South America Brazil Argentina Colombia Chile Venezuela Peru Puerto Rico Ecuador
Rest of the World Kazakhstan
Points Covered in The Report The points that are discussed within the report are the major market players that are involved in the market such as market players, raw material suppliers, equipment suppliers, end users, traders, distributors and etc. The complete profile of the companies is mentioned. And the capacity, production, price, revenue, cost, gross, gross margin, sales volume, sales revenue, consumption, growth rate, import, export, supply, future strategies, and the technological developments that they are making are also included within the report. This report analyzed 12 years data history and forecast. The growth factors of the market is discussed in detail wherein the different end users of the market are explained in detail. Data and information by market player, by region, by type, by application and etc, and custom research can be added according to specific requirements. The report contains the SWOT analysis of the market. Finally, the report contains the conclusion part where the opinions of the industrial experts are included.
Key Reasons to Purchase To gain insightful analyses of the market and have comprehensive understanding of the global market and its commercial landscape. Assess the production processes, major issues, and solutions to mitigate the development risk. To understand the most affecting driving and restraining forces in the market and its impact in the global market. Learn about the market strategies that are being adopted by leading respective organizations. To understand the future outlook and prospects for the market. Besides the standard structure reports, we also provide custom research according to specific requirements.
The report focuses on Global, Top 10 Regions and Top 50 Countries Market Size of Dicyclohexylcarbodiimide (DCC) 2016-2021, and development forecast 2022-2027 including industries, major players/suppliers worldwide and market share by regions, with company and product introduction, position in the market including their market status and development trend by types and applications which will provide its price and profit status, and marketing status & market growth drivers and challenges, with base year as 2020.
Key Indicators Analysed Market Players & Competitor Analysis: The report covers the key players of the industry including Company Profile, Product Specifications, Production Capacity/Sales, Revenue, Price and Gross Margin 2016-2021 & Sales by Product Types. Global and Regional Market Analysis: The report includes Global & Regional market status and outlook 2022-2027. Further the report provides break down details about each region & countries covered in the report. Identifying its production, consumption, import & export, sales volume & revenue forecast. Market Analysis by Product Type: The report covers majority Product Types in the Dicyclohexylcarbodiimide (DCC) Industry, including its product specifcations by each key player, volume, sales by Volume and Value (M USD). Markat Analysis by Application Type: Based on the Dicyclohexylcarbodiimide (DCC) Industry and its applications, the market is further sub-segmented into several major Application of its industry. It provides you with the market size, CAGR & forecast by each industry applications. Market Trends: Market key trends which include Increased Competition and Continuous Innovations. Opportunities and Drivers: Identifying the Growing Demands and New Technology Porters Five Force Analysis: The report will provide with the state of competition in industry depending on five basic forces: threat of new entrants, bargaining power of suppliers, bargaining power of buyers, threat of substitute products or services, and existing industry rivalry.
COVID-19 Impact Report covers Impact of Coronavirus COVID-19: Since the COVID-19 virus outbreak in December 2019, the disease has spread to almost every country around the globe with the World Health Organization declaring it a public health emergency. The global impacts of the coronavirus disease 2019 (COVID-19) are already starting to be felt, and will significantly affect the Dicyclohexylcarbodiimide (DCC) market in 2021. The outbreak of COVID-19 has brought effects on many aspects, like flight cancellations; travel bans and quarantines; restaurants closed; all indoor/outdoor events restricted; over forty countries state of emergency declared; massive slowing of the supply chain; stock market volatility; falling business confidence, growing panic among the population, and uncertainty about future.
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Hyperphosphatemia Drugs Market Status and Trend Analysis 2017-2026 (COVID-19 Version)
Due to the pandemic, we have included a special section on the Impact of COVID 19 on the Hyperphosphatemia Drugs Market Status and Trend Analysis 2017-2026 (COVID-19 Version) 2020-2026 which would mention How the Covid-19 is Affecting the Industry, Market Trends and Potential Opportunities in the COVID-19 Landscape, Key Regions and Proposal for Hyperphosphatemia Drugs Market Status and Trend Analysis 2017-2026 (COVID-19 Version) Players to battle Covid-19 Impact.
Hyperphosphatemia Drugs Market Status and Trend Analysis 2017-2026 (COVID-19 Version) 2020-2026The
Hyperphosphatemia Drugs Market Status and Trend Analysis 2017-2026 (COVID-19 Version) 2020-2026
report is one of the most comprehensive and important data about business strategies, qualitative and quantitative analysis of Global Market. It offers detailed research and analysis of key aspects of the Hyperphosphatemia Drugs Market Status and Trend Analysis 2017-2026 (COVID-19 Version). The market analysts authoring this report have provided in-depth information on leading growth drivers, restraints, challenges, trends, and opportunities to offer a complete analysis of the Hyperphosphatemia Drugs Market Status and Trend Analysis 2017-2026 (COVID-19 Version).
Top Leading players covered in the Hyperphosphatemia Drugs Market Status and Trend Analysis 2017-2026 (COVID-19 Version) report : Shire Keryx Biopharmaceuticals Sanofi Fresenius Medical Care Vifor Pharma Kyowa Hakko Kirin Japan Tobacco Torii Pharmaceutical Bayer Novartis Kissei Pharmaceutical Amgen Chugai Pharmaceutical Baxter Mylan Natco Opko Health and More...
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The report offers clear guidelines for players to cement a position of strength in the global Hyperphosphatemia Drugs Market Status and Trend Analysis 2017-2026 (COVID-19 Version). It prepares them to face future challenges and take advantage of lucrative opportunities by providing a broad analysis of market conditions. the global Hyperphosphatemia Drugs Market Status and Trend Analysis 2017-2026 (COVID-19 Version) will showcase a steady CAGR in the forecast year 2020 to 2026.
Market Segment by Type covers: Aluminum Phosphate Binder Iron Phosphate Binder Magnesium Phosphate Binder Calcium Phosphate Binder
Market Segment by Application covers: Hospitals Clinics Others
Our Complimentary Sample Hyperphosphatemia Drugs Market Status and Trend Analysis 2017-2026 (COVID-19 Version) Report Accommodate a Brief Introduction of the research report, TOC, List of Tables and Figures, Competitive Landscape and Geographic Segmentation, Innovation and Future Developments Based on Research Methodology.
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Regions Covered in the Global Hyperphosphatemia Drugs Market Status and Trend Analysis 2017-2026 (COVID-19 Version):
• The Middle East and Africa (GCC Countries and Egypt)
• North America (the United States, Mexico, and Canada)
• South America (Brazil etc.)
• Europe (Turkey, Germany, Russia UK, Italy, France, etc.)
• Asia-Pacific (Vietnam, China, Malaysia, Japan, Philippines, Korea, Thailand, India, Indonesia, and Australia)
Years Considered to Estimate the Hyperphosphatemia Drugs Market Status and Trend Analysis 2017-2026 (COVID-19 Version) Size:
History Year: 2015-2019
Base Year: 2019
Estimated Year: 2020
Forecast Year: 2020-2026
Highlights of the Report:
• Accurate market size and CAGR forecasts for the period 2019-2026
• Identification and in-depth assessment of growth opportunities in key segments and regions
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Best Translation Company in India
Delsh Business Consultancy is India's No.1 ISO certified Translation Company that provides accurate Language Translation services in Delhi India. We offer the world’s most accurate translation services to the global clients that are also the fastest in speed. Often, it is seen that the companies fail to render quality and precision in translation due to pricing rates, in making haste for the project delivery.
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Healthcare Packaging Market Consumption Analysis, Business Overview and Upcoming Trends 2030
The Healthcare Packaging market report provides a detailed analysis of global market size, regional and country-level market size, segmentation market growth, market share, competitive Landscape, sales analysis, impact of domestic and global market players, value chain optimization, trade regulations, recent developments, opportunities analysis, strategic market growth analysis, product launches, area marketplace expanding, and technological innovations.
The data in this report target business and industry practitioners and intended to assist in explanation, direction, and understanding of the potential of the plastic healthcare packaging markets. The study focuses on providing readers to understand of development in the industry.
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Global Healthcare Packaging Market: Major Players
Clondalkin Group Holdings
Catalent Pharma Solutions
Cardinal Health
American Health Packaging
Intrapac Group
RPC Group
Constantia Flexibles
EUROMEDEX
Amcor
NNE
Nypro Packaging
Schott
Nampak
Global Closure Systems
Gerresheimer
Korber
Datwyler Pharma Packaging
Vitro
Steripack
CWS Packaging
AptarGroup
BD
Barger Packaging
CCL Industries
Baxter
Menasha Packaging
Alexander
Klockner Pentaplast Group
Winpak
Bemis
Global Healthcare Packaging Market: By Types
Plastic bottles
Caps & closures
Blister packs
Pouches
Trays
Pre-fillable syringes
Parenteral containers
Clamshells
Pre-fillable inhalers
Medication tubes
Global Healthcare Packaging Market: By Applications
Medical Apparatus And Instruments
Medical Drugs
Medical Container
Global Healthcare Packaging Market: Regional Analysis
All the regional segmentation has been studied based on recent and future trends, and the market is forecasted throughout the prediction period. The countries covered in the regional analysis of the Global Healthcare Packaging market report are U.S., Canada, and Mexico in North America, Germany, France, U.K., Russia, Italy, Spain, Turkey, Netherlands, Switzerland, Belgium, and Rest of Europe in Europe, Singapore, Malaysia, Australia, Thailand, Indonesia, Philippines, China, Japan, India, South Korea, Rest of Asia-Pacific (APAC) in the Asia-Pacific (APAC), Saudi Arabia, U.A.E, South Africa, Egypt, Israel, Rest of Middle East and Africa (MEA) as a part of Middle East and Africa (MEA), and Argentina, Brazil, and Rest of South America as part of South America.
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The report focuses on Global, Top 10 Regions and Top 50 Countries Market Size of Healthcare Packaging including industries, major players/suppliers worldwide and market share by regions, with company and product introduction, position in the market including their market status and development trend by types and applications which will provide its price and profit status, and marketing status & market growth drivers and challenges, with base year as 2022.
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Hikma Pharmaceuticals Plc Company Market Analysis Report - Company Market size - Company profile
Hikma Pharmaceuticals Plc (Hikma) develops, manufactures and markets branded and non-branded generics and in-licensed products. The company specializes in the areas of cardiovascular, diabetes, central nervous system (CNS), cancer, dermatology, genitourinary system, hormones and respiratory system, among others. Hikma Pharmaceuticals market analysisHikma Pharmaceuticals Company Profile
It offers generics in various dosage forms including tablets, capsules, solutions and suspensions. Hikma Pharmaceuticals sells its products through sales and marketing teams and representatives to leading wholesalers, pharmacy chains, governments and hospital purchasing organizations. The company markets its products in the UK, the Middle East, and North Africa (MENA) and Europe and rest of the world. Hikma Pharmaceuticals is headquartered in London, the UK.
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Market Demand for Fluorine-18 Growth Trends Report by 2031
Fluorine-18 Market: Overview
According to the report, the global fluorine-18 market was valued over US$ 1.5 Bn in 2020 and is projected to expand at a CAGR of 7.5% from 2021 to 2031. Fluorine-18 is the most important radionuclide used in positron emission tomography (PET) today, largely due to its unique physical and nuclear characteristics. Agents such as the clinical oncology tracer FDG, the most widely used PET-radiopharmaceutical, have driven interest toward the chemistry of radiopharmaceuticals utilizing fluorine-18.
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Rise in Preference for PET/CT and PET Scans to Drive Global Market
PET/CT and PET are modern systems used to detect and treat cancer, cardiovascular diseases, and other neurology related diseases. Molecular imaging with novel radiopharmaceuticals has been engineered to target specific subcellular processes and improve diagnostic accuracy using radioactive molecule as a tracer in PET/CT scan. Hence, the preference for PET/CT scan is rising, which is anticipated to drive the global fluorine-18 market.
Lack of Availability and High Operating Expenses to Hamper Global Market
The limitations of FDG-PET are its lack of availability and high operating expenses. F-18 fluoride ion is created in a cyclotron, and then converted via an automated chemistry module into the F-18 FDG. The cost of establishing the PET/CT scan facility with cyclotron is around US$ 5 Mn to US$ 6 Mn.
FDG to Dominate Global Market
The global fluorine-18 market has been segmented based on product and end user. In terms of product, the global fluorine-18 market has been classified into FDG, NaF, and others. The FDG segment is expected to account for a major share of the global market by 2031, due to the increase in demand for PET/CT scan in oncology.
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Hospitals to be Major End User
In terms of end user, the global fluorine-18 market has been divided into hospitals, diagnostic centers, and others. The hospitals segment is likely to expand at a high CAGR during the forecast period, due to the increase in the demand for the installation of new PET-CT machines in the upcoming hospital projects across the globe, which drive the demand for F-18 isotopes.
North America to Dominate Global Market
The global fluorine-18 market has been segmented into five major regions: North America, Europe, Asia Pacific, Latin America, and Middle East & Africa. North America dominated the global fluorine-18 market in 2020, followed by Europe. The fluorine-18 market in Asia Pacific is projected to expand at a high CAGR from 2021 to 2031. Product launches, acquisitions, distribution agreements, alliances, and geographical expansion by local players, especially in China and India, are anticipated to drive the fluorine-18 market in the region.
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Competition Landscape
The report also presents profiles of leading players in the global fluorine-18 market. These include Lantheus Holdings, Inc., Siemens Healthineers, Advanced Accelerator Applications (a Novartis AG Company), GE Healthcare (General Electric Company), Blue Earth Diagnostics (A Bracco Imaging Company), Jubilant Pharma Limited, China lsotope & Radiation Corporation, Eli Lilly and Company, Curium Pharma, and Yantai Dongcheng Pharmaceutical Group Co., Ltd. The leading companies in the global fluorine-18 market focus on strengthening the distribution network and expanding product range to gain market share. For instance, in February 2018, Advanced Accelerator Applications signed an exclusive license agreement with the Cancer Targeted Technology to develop CTT1057, an F-18 labeled PSMA ligand for diagnostic applications in prostate cancer.
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Our data repository is continuously updated and revised by a team of research experts, so that it always reflects the latest trends and information. With a broad research and analysis capability, Transparency Market Research employs rigorous primary and secondary research techniques in developing distinctive data sets and research material for business reports.
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Fluorine-18 Market Size will Grow at a Robust Pace through 2031
According to the report, the global fluorine-18 market was valued over US$ 1.5 Bn in 2020 and is projected to expand at a CAGR of 7.5% from 2021 to 2031. Fluorine-18 is the most important radionuclide used in positron emission tomography (PET) today, largely due to its unique physical and nuclear characteristics. Agents such as the clinical oncology tracer FDG, the most widely used PET-radiopharmaceutical, have driven interest toward the chemistry of radiopharmaceuticals utilizing fluorine-18.
Request a Sample of Fluorine-18 Market: https://www.transparencymarketresearch.com/sample/sample.php?flag=S&rep_id=82266
Rise in Preference for PET/CT and PET Scans to Drive Global Market
PET/CT and PET are modern systems used to detect and treat cancer, cardiovascular diseases, and other neurology related diseases. Molecular imaging with novel radiopharmaceuticals has been engineered to target specific subcellular processes and improve diagnostic accuracy using radioactive molecule as a tracer in PET/CT scan. Hence, the preference for PET/CT scan is rising, which is anticipated to drive the global fluorine-18 market.
Enquiry before Buying Fluorine-18 Market Report - https://www.transparencymarketresearch.com/sample/sample.php?flag=EB&rep_id=82266
Lack of Availability and High Operating Expenses to Hamper Global Market
The limitations of FDG-PET are its lack of availability and high operating expenses. F-18 fluoride ion is created in a cyclotron, and then converted via an automated chemistry module into the F-18 FDG. The cost of establishing the PET/CT scan facility with cyclotron is around US$ 5 Mn to US$ 6 Mn.
FDG to Dominate Global Market
The global fluorine-18 market has been segmented based on product and end user. In terms of product, the global fluorine-18 market has been classified into FDG, NaF, and others. The FDG segment is expected to account for a major share of the global market by 2031, due to the increase in demand for PET/CT scan in oncology.
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Hospitals to be Major End User
In terms of end user, the global fluorine-18 market has been divided into hospitals, diagnostic centers, and others. The hospitals segment is likely to expand at a high CAGR during the forecast period, due to the increase in the demand for the installation of new PET-CT machines in the upcoming hospital projects across the globe, which drive the demand for F-18 isotopes.
North America to Dominate Global Market
The global fluorine-18 market has been segmented into five major regions: North America, Europe, Asia Pacific, Latin America, and Middle East & Africa. North America dominated the global fluorine-18 market in 2020, followed by Europe. The fluorine-18 market in Asia Pacific is projected to expand at a high CAGR from 2021 to 2031. Product launches, acquisitions, distribution agreements, alliances, and geographical expansion by local players, especially in China and India, are anticipated to drive the fluorine-18 market in the region.
Buy now Fluorine-18 Market Report - https://www.transparencymarketresearch.com/checkout.php?rep_id=82266<ype=S
Competition Landscape
The report also presents profiles of leading players in the global fluorine-18 market. These include Lantheus Holdings, Inc., Siemens Healthineers, Advanced Accelerator Applications (a Novartis AG Company), GE Healthcare (General Electric Company), Blue Earth Diagnostics (A Bracco Imaging Company), Jubilant Pharma Limited, China lsotope & Radiation Corporation, Eli Lilly and Company, Curium Pharma, and Yantai Dongcheng Pharmaceutical Group Co., Ltd. The leading companies in the global fluorine-18 market focus on strengthening the distribution network and expanding product range to gain market share. For instance, in February 2018, Advanced Accelerator Applications signed an exclusive license agreement with the Cancer Targeted Technology to develop CTT1057, an F-18 labeled PSMA ligand for diagnostic applications in prostate cancer.
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Smart Insulin Pens Market
https://www.prnewswire.com/news-releases/rising-diabetic-patients-pool-prompts-high-demand-for-smart-insulin-pens-market-estimated-to-be-valued-at-us-70-4-mn-by-2027-end-tmr-301316368.html
Radiation Dermatitis Market
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Electronic Clinical Outcome Assessment Market Share, Industry Growth, Trend, Drivers, Challenges, Key Companies by 2026
The Global Electronic Clinical Outcome Assessment (eCOA) Solutions Market Report added by Reports and Data offers extensive knowledge and information about the Electronic Clinical Outcome Assessment (eCOA) Solutions market with regards to market size, market share, growth influencing factors, opportunities, demands, consumer behavior, market drivers and restraints, overall competitive landscape, and current and emerging trends. The research study offers valuable insights into the business strategies, distribution channels, and value chain analysis. The report also offers positive projections of the market scenario in the coming years through in-depth assessment of the key markets features and the geographical spread of the industry. The report strives to present the reader with deep insights of the market that can assist them in making fruitful business decisions and strategic investment plans.
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The Electronic Clinical Outcome Assessment (eCOA) Solutions market report offers key insights into market scope along with emerging growth opportunities over the forecast period. The report also provides information about the competitive landscape of the global Electronic Clinical Outcome Assessment (eCOA) Solutions market. The global Electronic Clinical Outcome Assessment (eCOA) Solutions market is fragmented due to presence of numerous key players on a global and regional scale. Key players are focused on mergers and acquisitions, joint ventures, collaborations, partnerships, and research and development activities to expand their product portfolio and gain a robust footing in the market.
Key Companies Operating in the Electronic Clinical Outcome Assessment (eCOA) Solutions Market and profiled in the report are:
OmniComm Systems, eClinical solutions, CRF Health, Oracle Corporation, Paraxel International Corporation, Kayentis, Medidata Solution, Inc., Merge Healthcare Incorporated and ERT Clinical.
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The report provides a significant assessment of the recent market trends, revenues, segments, and key regions across the globe. The regional analysis covers major geographical regions such as North America, Europe, Asia Pacific, Latin America, and Middle East & Africa. The report analyzes key regions for production and consumption patterns, import/export, market share, revenue contribution, growth rate, and supply and demand ratio for the forecast period 2021-2028. It also discusses the impact of government regulations, macro- and micro-economic factors, and economic growth of the region on overall market growth.
Regional analysis covers:
North America (U.S.A., Canada)
Europe (U.K., Italy, Germany, France, Rest of Europe)
Asia Pacific (India, Japan, China, South Korea, Australia, Rest of APAC)
Latin America (Chile, Brazil, Argentina, Rest of Latin America)
Middle East & Africa (Saudi Arabia, U.A.E., South Africa, Rest of MEA)
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Type (Revenue, USD Million; 2018-2026)
Web-based Solution
Licensed Industries
Cloud-based
Application Outlook (Revenue, USD Million; 2018-2026)
Hospitals
Contract Research Organizations
Academic institutes
Pharma and biotech companies
Medical Device Manufacturers
Key Questions Answered by the Report:
What was the market size of the global Electronic Clinical Outcome Assessment (eCOA) Solutions market in 2020? At what rate is the market expected to grow over the forecast period?
What are the key growth driving and restraining factors of the Electronic Clinical Outcome Assessment (eCOA) Solutions market?
What are key opportunities and growth prospects of the Electronic Clinical Outcome Assessment (eCOA) Solutions industry is expected to witness over the forecast period?
Who are the prominent players operating in the market? What are the key strategies adopted by these companies?
Which region is expected to dominate the market growth over the forecast period?
Which segments are expected to register lucrative growth over the forecast period?
What are the key outcomes of SWOT analysis and Porter’s Five Forces analysis?
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