Global Industrial and Market Analysis Study on Clinical Trial Management System: Asia to Witness Highest Growth by 2019

"Global Market Study on Clinical Trial Management System: Asia to Witness Highest Growth by 2019" The Report covers current Industries Trends, Worldwide Analysis, Global Forecast, Review, Share, Size, Growth, Effect.

Description-

Clinical trial is a medical research study performed on humans to check the safety and efficacy of drugs, devices and therapeutic products before they are finally launched in the market. Proper management of clinical trials has become a priority for hospitals, pharmaceutical companies and clinical research organizations (CRO).Clinical trial management system (CTMS) is a software solution for proper management, storage and analysis of drugs associated clinical data. CTMS is primarily employed to manage the large amount of data involved in a clinical trial including planning, preparation and reporting. CTMS also provides data to a business intelligence system. It provides a user-friendly infrastructure that enables clinicians to manage trials of varying complexity.

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North America is a traditional clinical trial region. The percentage share of global clinical trials conducted in North America has reduced. This was due to regulatory and legal considerations, which shifted the clinical trial market from North America to developing countries such as India and China. Countries in Central and Eastern Europe provide abundant opportunities to life science companies for clinical development. Similarly, improved industry regulatory laws and patent expiration laws in various countries including Japan, China and India, have led to the expansion of the clinical trials market in Asia, which has lower cost of conducting clinical trials compared to Europe or the U.S.

Increasing R&D investment in pharmaceuticals, life science and clinical research industries, rising prevalence of diseases and increased clinical research outsourcing are key growth drivers for the CTMS market. In addition, integration of CTMS with a Hospital Information System (HIS) provides more accurate and time saving documentation over paper based information systems. On the other hand, long approval time for clinical trials and difficulties related to recruiting and enrolling patients for clinical trials are some of the major concerns for the industry. Approval from Institutional Review Board (IRB), contract and budget negotiation and approval, availability of appropriate patient population and protocol design and legal review are major factors that delay a drug approval process. Similarly, increasing regulatory requirements in many countries has resulted in increased complexity for clinical trial protocols.

This report provides an in-depth analysis of estimation of the CTMS market for the period 2013-2019, considering 2013 as the base year for calculation. In addition, data pertaining to current market dynamics including market drivers, restraints, trends and recent developments has been provided in the report. The CTMS market is categorized on the basis of type of CTMS, end users, components, mode of delivery and geography. Based on mode of delivery, the CTMS market comprises on-premise CTMS, Web based CTMS and cloud based CTMS. The end user market comprises pharmaceuticals, clinical research organizations and healthcare providers.

In the geographical analysis, the report identifies and analyses market size and forecast of North America, Europe, Asia and Rest of the World (RoW). North America is further segmented into the U.S. and rest of North America. Similarly, Europe is further segmented into Germany, France and Poland. Asia is further segmented into South Korea and China. Some of the major players in the CTMS market are Oracle Corporation, Bio-Optronics, MedNet Solutions, PAREXEL International Corporation, Medidata Solutions and BioClinica. These key market players have been profiled on the basis of attributes such as company overview, recent developments, growth strategies, sustainability and financial overview.

Table of Contents

Chapter 1 Preface 12
1.1 Report Description 12
1.2 Research Methodology 13
1.3 Assumptions 13

Chapter 2 Market Synopsis 14

Chapter 3 Porter Five Forces Analysis 16
3.1 Bargaining power of suppliers 16
3.2 Bargaining power of buyers 16
3.3 Threat of new entrants 17
3.4 Threat of substitutes 17
3.5 Intensity of rivalry 17

Chapter 4 Industry Overview 18
4.1 Market Definition 18
4.2 Market Drivers 20
4.2.1 Increasing research and development (R&D) investment in the pharmaceutical industry 20
4.2.2 Increasing prevalence of disease is supporting importance of clinical trials in different regions of the world 22
4.2.3 Assimilation of clinical trial management systems with Hospital Information System (HIS) 22
4.2.4 Increased clinical research outsourcing and implementation of clinical trials by contract research organizations 23
4.3 Impact Analysis of Market Drivers 24
4.4 Market Restraints 24
4.4.1 Longer approval time for clinical trials 24
4.4.2 Strict regulations to enrol patients for clinical trials 25
4.5 Impact Analysis of Market Restraints 26
4.6 Market Trends 26
4.6.1 Rising number of collaborations and partnerships 26
4.6.2 Increasing number of mergers and acquisitions 27

Chapter 5 Global Market Size and Forecast 29

Chapter 6 Market Size and Forecast by Mode of Delivery 31
6.1 Cloud based clinical trial management system 31
6.2 Web based clinical trial management system 32
6.3 On-premise clinical trial management system 32

Chapter 7 Market Size and Forecast by End User 34
7.1 Pharmaceuticals 34
7.2 Clinical Research Organizations (CROs) 34
7.3 Healthcare Providers 35

Chapter 8 Market Size and Forecast by Type 37
8.1 Enterprise based clinical trial management system 37
8.2 Site based clinical trial management system 37

Chapter 9 Market Size and Forecast by Components 39
9.1 Software 39
9.2 Hardware 40
9.3 Services 40

Chapter 10 Market Size and Forecast by Geography 42
10.1 North America 42
10.1.1 The U.S. 49
10.2 Europe 53
10.2.1 Germany 61
10.2.2 France 65
10.2.3 Poland 68

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