表紙:臨床試験管理システム(CTMS)の世界市場予測(2022年~2027年)
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臨床試験管理システム(CTMS)の世界市場予測(2022年~2027年)

Global Clinical Trial Management System (CTMS) Market - Forecasts from 2022 to 2027

出版日: | 発行: Knowledge Sourcing Intelligence | ページ情報: 英文 100 Pages | 納期: 即日から翌営業日

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臨床試験管理システム(CTMS)の世界市場予測(2022年~2027年)
出版日: 2022年03月09日
発行: Knowledge Sourcing Intelligence
ページ情報: 英文 100 Pages
納期: 即日から翌営業日
  • 全表示
  • 概要
  • 目次
概要

世界の臨床試験管理システム(CTMS)の市場規模は、2020年は12億839万1,000米ドルで、予測期間中に12.51%のCAGRで成長し、2027年には27億5,769万1,000米ドルに達すると予測されています。

当レポートでは、世界の臨床試験管理システム(CTMS)市場を調査しており、市場の概要、市場規模や予測、動向、成長要因および抑制要因、タイプ・配信モード・コンポーネント・エンドユーザー・用途・地域別の分析、および競合情勢などを提供しています。

目次

第1章 イントロダクション

  • 市場の定義
  • 市場セグメンテーション

第2章 調査手法

  • 調査データ
  • 前提条件

第3章 エグゼクティブサマリー

  • 調査のハイライト

第4章 市場力学

  • 市場促進要因
  • 市場抑制要因
  • ポーターのファイブフォース分析
    • エンドユーザーの交渉力
    • 買い手の交渉力
    • 新規参入業者の脅威
    • 代替品の脅威
    • 業界における競合情勢
  • 業界のバリューチェーン分析

第5章 世界の臨床試験管理システム(CTMS)市場分析:タイプ別

  • イントロダクション
  • 企業CTMS
  • サイトCTMS

第6章 世界の臨床試験管理システム(CTMS)市場分析:配信モード別

  • イントロダクション
  • オンプレミス
  • クラウドベース

第7章 世界の臨床試験管理システム(CTMS)市場分析:コンポーネント別

  • イントロダクション
  • ソフトウェア
  • サービス

第8章 世界の臨床試験管理システム(CTMS)市場分析:エンドユーザー別

  • イントロダクション
  • 製薬・バイオテクノロジー企業
  • 委託研究機関
  • 医療機器メーカー
  • その他

第9章 世界の臨床試験管理システム(CTMS)市場分析:地域別

  • イントロダクション
  • 北米
    • 米国
    • カナダ
    • メキシコ
  • 南米
    • ブラジル
    • アルゼンチン
    • その他
  • 欧州
    • ドイツ
    • フランス
    • 英国
    • イタリア
    • スペイン
    • その他
  • 中東とアフリカ
    • サウジアラビア
    • アラブ首長国連邦
    • 南アフリカ
    • その他
  • アジア太平洋
    • 中国
    • インド
    • 日本
    • 韓国
    • 台湾
    • タイ
    • インドネシア
    • その他

第10章 競合環境と分析

  • 主要企業と戦略分析
  • 新興企業と市場の収益性
  • 合併、買収、合意、およびコラボレーション
  • ベンダー競争力マトリックス

第11章 企業プロファイル

  • ArisGlobal LLC
  • RealTime Software Solutions LLC
  • Breeze CTMS
  • Veeva Systems
  • Oracle Corporation
  • Business Systems Integration AG
  • Ennov
  • Bioclinica
  • IBM Corporation
  • Bio-Optronics Inc.
目次
Product Code: KSI061612086

The global clinical trial management system (CTMS) market was valued at US$1,208.391 million in 2020 and is expected to grow at a CAGR of 12.51% over the forecast period to reach a total market size of US$2,757.691 million by 2027.

The Clinical Trial Management System (CTMS) is a software system used by biotechnology and pharmaceutical industries to handle clinical trials in clinical research. The system keeps track of and handles planning, performance, and reporting tasks, as well as participant contact information and deadlines and milestones. ClinicalTrials currently lists 391,704 studies with sites in all 50 states and 219 countries.

The increased prevalence of chronic and lifestyle-related disorders, as well as a surge in clinical trial outsourcing and implementation by contract research companies, are driving market expansion. According to the Food and Agriculture Organization (FAO), chronic diseases will account for nearly three-quarters of all deaths worldwide by 2020, with developing countries accounting for 71% of deaths due to ischaemic heart disease (IHD), 75% of deaths due to stroke, and 70% of deaths due to diabetes. Diabetics will increase more than 2.5 times in the developing world, from 84 million in 1995 to 228 million in 2025. Globally, developing nations will bear 60% of the burden of chronic disorders. Furthermore, according to the World Health Organization 2020, major chronic illnesses such as heart disease, stroke, cancer, diabetes, and chronic lung disease account for about 70% of all fatalities globally. Almost three-quarters of all non-communicable disease (NCD) deaths occur in low- and middle-income countries, as do 82% of the 16 million individuals who died prematurely, or before reaching the age of 70.

Furthermore, increasing innovative technology developments to reduce the rising cost of clinical trials have resulted in the development of the clinical trial management system. Although these systems have not been fully adopted owing to a variety of reasons, increasing awareness and the desire to reduce additional expenses associated with clinical trials are likely to boost the market in the future. However, data security concerns and the high cost of clinical trial administration systems are expected to limit market development.

The overall clinical trial management systems market is projected to be dominated by North America. Factors such as increased R&D spending and an increase in demand for medication development are assisting in the expansion of the country's industry under study. According to WHO, 147,213 trials took place in the United States in 2020, which was the highest for any country, followed by 23,051 trials in China and 13,481 in Japan. The growing number of studies and clinical trials, along with increased financing for clinical research, is expected to fuel market growth.

Growth Factors

  • A Growing Number of Clinical Trials:

The increasing number of clinical trials, combined with the availability of sophisticated CTMS systems, is expected to drive market growth. According to WHO, there have been 61,311 trials worldwide in 2020, with a cumulative total of 600,173 trials since 1999. Thus, the increasing number of clinical research studies will boost the use of clinical trial management system solutions, therefore increasing market value. Furthermore, the demand for effective data management and clinical trial result analysis are a few other aspects that are expected to add to market revenue. The deployment and expense of a clinical trial management system, on the other hand, may hinder the market's development.

Restraints:

Budget constraints and high cost Due to limited private financing, stringent regulations, and a bleak financial future, small and mid-sized client facilities frequently encounter budgetary restrictions for clinical trials. Ineffective site selection, poor research design and trial execution, safety concerns, and dropouts due to practical or budgetary constraints are additional instances. Furthermore, the amount of time and money necessary to finish a study grows with each phase. The overall cost of a Phase III failure includes the costs of all previous stages as well as the time that might have been spent testing an alternative medication. According to WHO, as of 2020, 62,603 trials are in Phase III development. Small pharma companies (those with less than $500 million in annual revenue) now account for more than 70% of the roughly 3,000 medicines in phase III clinical trials. Only approximately 20% of medicines now in phase III clinical trials have been launched by large pharma companies (those with annual revenues of $1 billion or more). Each failed study adds to the ever-increasing costs of biopharma R&D. The Congressional Budget Office estimates that in 2019, the pharmaceutical sector spent $83 billion on research and development. The projected cost of developing new medication, including capital expenses and spending on drugs that do not reach the market, ranges from less than $1 billion to more than $2 billion.

COVID-19's Impact on the Clinical Trial Management System (CTMS) Market:

In the midst of the COVID-19 pandemic, the healthcare systems of countries are quickly investing in research and development to battle the virus. Potential chemicals were selected from the CHEMBL and ZINC databases, as well as FDA-approved medicines and molecules in clinical studies. As a result, COVID-19 is projected to have a favourable influence on market growth throughout the forecast period. Cytel Inc. deployed an open-access global COVID-19 Clinical Trial Tracker in April 2020, facilitating massive cooperation among academics, policymakers, doctors, journalists, philanthropists, and other important stakeholders. Similarly, asthe battle to discover an easy-to-administer therapy for the potentially deadly infection heats up, Pfizer Inc and Merck & Co Inc launched additional studies of their investigational oral antiviral medicines for COVID-19 in September 2021.

Key Developments

  • September 2021: PHARMASEAL International Ltd. and Medrio, Inc. collaborated to integrate Medrio's eClinical data collectionsuite with PHARMASEAL's trial management platform, Englity®.
  • August 2021: Verily, an Alphabet subsidiary, has agreed to acquire SignalPath, a clinical trial management system (CTMS) based in Raleigh, North Carolina, that improves the accessibility, quality, and efficiency of clinical research at study sites.

Market Segmentation

  • By Type

Enterprise CTMS

Site CTMS

  • By Delivery Mode

On-premise

Cloud-based

  • By Component

Software

Services

  • By End-User

Pharmaceutical and Biotechnology Companies

Contract Research Organizations

Medical Device Manufacturers

Others

  • By Geography

North America

  • USA
  • Canada
  • Mexico

South America

  • Brazil
  • Argentina
  • Others

Europe

  • Germany
  • France
  • UK
  • Italy
  • Spain
  • Others

Middle East and Africa

  • Saudi Arabia
  • UAE
  • South Africa
  • Others

Asia Pacific

  • China
  • India
  • Japan
  • South Korea
  • Taiwan
  • Thailand
  • Indonesia
  • Others

TABLE OF CONTENTS

1. Introduction

  • 1.1. Market Definition
  • 1.2. Market Segmentation

2. Research Methodology

  • 2.1. Research Data
  • 2.2. Assumptions

3. Executive Summary

  • 3.1. Research Highlights

4. Market Dynamics

  • 4.1. Market Drivers
  • 4.2. Market Restraints
  • 4.3. Porters Five Forces Analysis
    • 4.3.1. Bargaining Power of End-Users
    • 4.3.2. Bargaining Power of Buyers
    • 4.3.3. Threat of New Entrants
    • 4.3.4. Threat of Substitutes
    • 4.3.5. Competitive Rivalry in the Industry
  • 4.4. Industry Value Chain Analysis

5. Global Clinical Trial Management System (CTMS) Market Analysis, by Type

  • 5.1. Introduction
  • 5.2. Enterprise CTMS
  • 5.3. Site CTMS

6. Global Clinical Trial Management System (CTMS) Market Analysis, by Delivery Mode

  • 6.1. Introduction
  • 6.2. On-premise
  • 6.3. Cloud-based

7. Global Clinical Trial Management System (CTMS) Market Analysis, by Component

  • 7.1. Introduction
  • 7.2. Software
  • 7.3. Services

8. Global Clinical Trial Management System (CTMS) Market Analysis, by End-User

  • 8.1. Introduction
  • 8.2. Pharmaceutical and Biotechnology Companies
  • 8.3. Contract Research Organizations
  • 8.4. Medical Device Manufacturers
  • 8.5. Others

9. Global Clinical Trial Management System (CTMS) Market Analysis, by Geography

  • 9.1. Introduction
  • 9.2. North America
    • 9.2.1. USA
    • 9.2.2. Canada
    • 9.2.3. Mexico
  • 9.3. South America
    • 9.3.1. Brazil
    • 9.3.2. Argentina
    • 9.3.3. Others
  • 9.4. Europe
    • 9.4.1. Germany
    • 9.4.2. France
    • 9.4.3. UK
    • 9.4.4. Italy
    • 9.4.5. Spain
    • 9.4.6. Others
  • 9.5. Middle East and Africa
    • 9.5.1. Saudi Arabia
    • 9.5.2. UAE
    • 9.5.3. South Africa
    • 9.5.4. Others
  • 9.6. Asia Pacific
    • 9.6.1. China
    • 9.6.2. India
    • 9.6.3. Japan
    • 9.6.4. South Korea
    • 9.6.5. Taiwan
    • 9.6.6. Thailand
    • 9.6.7. Indonesia
    • 9.6.8. Others

10. Competitive Environment and Analysis

  • 10.1. Major Players and Strategy Analysis
  • 10.2. Emerging Players and Market Lucrativenessness
  • 10.3. Mergers, Acquisitions, Agreements, and Collaborations
  • 10.4. Vendor Competitiveness Matrix

11. Company Profiles 

  • 11.1. ArisGlobal LLC
  • 11.2. RealTime Software Solutions LLC
  • 11.3. Breeze CTMS
  • 11.4. Veeva Systems
  • 11.5. Oracle Corporation
  • 11.6. Business Systems Integration AG
  • 11.7. Ennov
  • 11.8. Bioclinica
  • 11.9. IBM Corporation
  • 11.10. Bio-Optronics Inc.