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医薬品受託製造開発機関(CDMO)市場 - 成長、トレンド、および予測(2020年~2025年)

Pharmaceutical Contract Development and Manufacturing Organization (CDMO) Market - Growth, Trends, Forecasts (2020 - 2025)

発行 Mordor Intelligence LLP 商品コード 866699
出版日 ページ情報 英文 120 Pages
納期: 2-3営業日
価格
本日の銀行送金レート: 1USD=107.71円で換算しております。
医薬品受託製造開発機関(CDMO)市場 - 成長、トレンド、および予測(2020年~2025年) Pharmaceutical Contract Development and Manufacturing Organization (CDMO) Market - Growth, Trends, Forecasts (2020 - 2025)
出版日: 2020年06月01日 ページ情報: 英文 120 Pages
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概要

当レポートでは、医薬品受託製造開発機関(CDMO)について調査しており、市場概況や今後の動向、競合情勢、CMO市場でのサービス種類別、CRO市場での調査フェーズ別、地域別の市場分析、CMOおよびCROベンダーの主要企業のプロファイル等をまとめています。

目次

第1章 イントロダクション

  • 研究成果
  • 調査の前提条件
  • 調査範囲

第2章 調査方法

第3章 エグゼクティブサマリー

第4章 市場のダイナミクス

  • 市場概況
  • 市場成長および阻害要因のイントロダクション
  • 市場成長要因
    • 大手製薬会社別アウトソーシング量の増加
    • アウトソーシングモデルへのCDMOモデルの到来
    • 研究開発への投資の増加
  • 市場の阻害要因
    • リードタイムと物流コストの増加
    • 厳しい規制要件
    • CMOSの収益性に影響する容量利用の問題
  • 業界バリューチェーン分析
  • 業界の魅力 - ポーターファイブフォース分析
    • 新規参入の脅威
    • バイヤー/消費者の交渉力
    • サプライヤーの交渉力
    • 代替製品の脅威
    • 業界内の競争
  • 業界ポリシー
  • 技術スナップショット
    • 投与量処方テクノロジー
    • 投与経路別剤形
    • 製薬研究開発のアウトソーシングに関する主に考慮すべき事項
    • CROの主なセグメント - バイオ分析試験、セントラル・ラボでの試験およびcGMP試験

第5章 市場セグメント

  • サービスの種類別 - CMO市場セグメント
    • 医薬品原薬(API)の製造
    • 完成した投与量製剤(FDF)の開発と製造
    • 二次包装
  • 調査フェーズ別 - CRO市場セグメント
    • 前臨床
    • フェーズI
    • フェーズII
    • フェーズIII
    • フェーズIV
  • 地域別
    • CMO市場セグメント
    • CROセグメント用

第6章 競合情勢

  • 企業プロファイル
    • CMOベンダー
    • CROベンダー

第7章 投資分析

第8章 市場機会および今後の動向

目次
Product Code: 66565

The Pharmaceutical CDMO market was valued USD 148.5 billion in 2019, and it is expected to reach USD 224.9 billion by 2025, registering a CAGR of 7%, during the period of 2020-2025.

  • As a result of the growing demand for generic medicines and biologics, the capital-intensive nature of the business, and the complex manufacturing requirements, many pharmaceutical companies have identified the potential profitability in contracting with a CMO (contract manufacturing outsourcing) for both clinical and commercial stage manufacturing.
  • The biggest factor driving the growth of CMOs in the pharmaceutical industry is the growing need for state-of-the-art processes and production technologies, which have proven highly effective in meeting regulatory requirements.
  • US is one of the largest R&D spenders in the pharmaceutical and biotechnology sector. According to Axios, a prominent online news company in the United States, as of 2018, pharmaceutical industries in the country had the tenth-highest average after-tax profit levels, when compared to more than 100 different industries. While drug companies are responsible for 23% of the US health revenue, they also make 63% of the total profits.
  • R&D sections of several pharmaceutical companies, especially operating at small scales, were condensed after the emergence of CRO players. As more CROs have started to offer research services with valuable cost, they won the competition with in-house pharmaceutical R&D departments. CROs also follow several strategies to stay ahead of top pharmaceutical players.
  • The CMO/CDMO service sector is uniquely positioned to address some of the challenges that drug developers are facing amid the COVID-19 pandemic. This pandemic has impacted multiple aspects of the pharma and biopharma industry, from drug development, clinical trials, supplies, manufacturing, to supply chain logistics. However, the drug shortages due to COVID-19 are limited, and they are expected to remain so for short-term, due to stockpiles of pharmaceuticals, APIs, globally.

Key Market Trends

Increasing Investment in R&D to Drive the Market Growth

  • The United States is the world's largest market for drugs, and accounts for almost half of the R&D spending in the pharmaceutical and biotechnology markets. Hence, CMOs play a critical role in this market and have invested in new facilities and technologies to cater to a wide range of outsourcing units.
  • The biggest Chinese professional manufacturer of dermatology and anti-tuberculosis drug products, Huapont, is one of the fastest-growing pharmaceutical manufacturers in China, mainly dependent on product R&D and market expansion.
  • CRO/CMOs are able toleverage their expertise, owing to their R&D and complex manufacturing capabilities, to fill the needs of the large generic, big pharmaceutical and biotech companies.
  • A major stake of R&D investments as well as capacity expansions, are likely in the injectable and sterile liquid dose formulations segment. Small biotech firms get access to specialized knowledge and resources, which help them expedite their R&D activities.

Asia-Pacific Expected to Witness Highest Growth in CRO Market

  • Over the forecast period, Asia-Pacific is expected to witness the highest growth in the CRO market, owing to the low cost offered by the region, as compared to the United States and other developed economies. Additionally, growing incidences of chronic and lifestyle diseases, such as diabetes and heart disease, coupled with ease of patient recruitment and availability of expertise for clinical trials, are few driving factors boosting growth in the region.
  • With increasing privatization of clinical trials, there has been an increase in the outsourcing of research processes in developing regions, such as China and India. For instance, the market is witnessing increased outsourcing of research services, such as Clinical Data Management, Pharmacovigilance, Biostatistics, etc., by large pharmaceuticals.
  • Growing investments by several pharmaceutical and biopharmaceutical drugs manufacturing companies are also supporting the growth of the CRO market in the region. As part of its five-year Research, Innovation, and Enterprise 2020 plan, the Singaporean government has committed to invest nearly USD 2.4 billion, in advancing manufacturing and engineering in the pharmaceutical market.
  • In January 2019, Lambda, headquartered in India, announced the acquisition of US-based Novum Pharmaceutical Research Services, in a move to increase its presence in the United States.

Competitive Landscape

The CDMO Market is consolidated in nature. The need for continued research and development related expenses push forward for the extension of business opportunities. In the pharmaceutical industry, medicine is continuously tested and are most profitable during the patent period, the emergence of competitive solution can hamper the rate of return. Such factors push for continued innovation and fast track the introduction time to market. Major players include Catalent Inc., Recipharm AB, Jubilant Life Sciences Ltd., among others.

  • February 2020 - Catalent, has signed an agreement with Zumutor Biologics, Inc., to manufacture Zumutor's, ZM008, for the treatment of solid tumors. Zumutor is a biologics company that develops novel immuno-oncotherapeutics to drive transformational improvements in cancer treatment.
  • December 2019 - Thermo Fisher Scientific Inc. opened its new USD 90 million viral vector CDMO (contract development and manufacturing organization) site in Lexington, Mass. The 50,000-square-foot facility will add more than 200 jobs and support the development, testing and manufacture of viral vectors, which are critical to advancing new life-saving gene and cell therapies worldwide.

Reasons to Purchase this report:

  • The market estimate (ME) sheet in Excel format
  • 3 months of analyst support

Table of Contents

1 INTRODUCTION

  • 1.1 Study Assumptions and Market Definition
  • 1.2 Scope of the Study

2 RESEARCH METHODOLOGY

3 EXECUTIVE SUMMARY

4 MARKET DYNAMICS

  • 4.1 Market Overview
  • 4.2 Industry Attractiveness - Porter's Five Forces Analysis
    • 4.2.1 Porter's Five Forces Analysis for CMO
    • 4.2.2 Porter's Five Forces Analysis for CRO
  • 4.3 Industry Value Chain Analysis
  • 4.4 Industry Policies
  • 4.5 Market Drivers
  • 4.6 Market Restraints
  • 4.7 Assessment of Impact of Covid-19 on the Industry

5 TECHNOLOGY SNAPSHOT

  • 5.1 Dosage Formulation Technologies
  • 5.2 Dosage Forms by Route of Administration
  • 5.3 Key Considerations for Outsourcing of Pharmaceutical R&D
  • 5.4 Major Segments in CRO - Bio Analytical Testing, Central Laboratory Testing, and cGMP Testing

6 MARKET SEGMENTATION

  • 6.1 Service Type - CMO Segment
    • 6.1.1 Active Pharmaceutical Ingredient (API) Manufacturing
    • 6.1.2 Finished Dosage Formulation (FDF) Development & Manufacturing
      • 6.1.2.1 Solid Dose Formulation
      • 6.1.2.2 Liquid Dose Formulation
      • 6.1.2.3 Injectable Dose Formulation
    • 6.1.3 Secondary Packaging
  • 6.2 Research Phase - CRO Segment
    • 6.2.1 Pre-clinical
    • 6.2.2 Phase I
    • 6.2.3 Phase II
    • 6.2.4 Phase III
    • 6.2.5 Phase IV
  • 6.3 Geography
    • 6.3.1 For CMO Market Segment
      • 6.3.1.1 North America
      • 6.3.1.1.1 By Service Type
      • 6.3.1.1.2 By Country
      • 6.3.1.1.2.1 United States
      • 6.3.1.1.2.2 Canada
      • 6.3.1.2 Europe
      • 6.3.1.2.1 By Service Type
      • 6.3.1.2.2 By Country
      • 6.3.1.2.2.1 United Kingdom
      • 6.3.1.2.2.2 Germany
      • 6.3.1.2.2.3 France
      • 6.3.1.2.2.4 Italy
      • 6.3.1.2.2.5 Rest of Europe
      • 6.3.1.3 Asia-Pacific
      • 6.3.1.3.1 By Service Type
      • 6.3.1.3.2 By Country
      • 6.3.1.3.2.1 China
      • 6.3.1.3.2.2 India
      • 6.3.1.3.2.3 Japan
      • 6.3.1.3.2.4 Australia
      • 6.3.1.3.2.5 Rest of Asia-Pacific
      • 6.3.1.4 Latin America
      • 6.3.1.4.1 By Service Type
      • 6.3.1.4.2 By Country
      • 6.3.1.4.2.1 Brazil
      • 6.3.1.4.2.2 Mexico
      • 6.3.1.4.2.3 Argentina
      • 6.3.1.4.2.4 Rest of Latin America
      • 6.3.1.5 Middle East and Africa
      • 6.3.1.5.1 By Service Type
      • 6.3.1.5.2 By Country
      • 6.3.1.5.2.1 United Arab Emirates
      • 6.3.1.5.2.2 Saudi Arabia
      • 6.3.1.5.2.3 South Africa
      • 6.3.1.5.2.4 Rest of Middle East and Africa
    • 6.3.2 For CRO Segment
      • 6.3.2.1 North America
      • 6.3.2.2 Europe
      • 6.3.2.3 Asia-Pacific
      • 6.3.2.4 Latin America
      • 6.3.2.5 Middle East and Africa

7 COMPETITIVE LANDSCAPE

  • 7.1 Vendor Market Share Analysis
  • 7.2 Company Profiles
    • 7.2.1 CMO Vendors
      • 7.2.1.1 Catalent Inc.
      • 7.2.1.2 Recipharm AB
      • 7.2.1.3 Jubilant Life Sciences Ltd.
      • 7.2.1.4 Patheon Inc.
      • 7.2.1.5 Boehringer Ingelheim Group
      • 7.2.1.6 Pfizer CentreSource
      • 7.2.1.7 Aenova Holding GmbH
      • 7.2.1.8 Famar SA
      • 7.2.1.9 Baxter Biopharma Solutions
      • 7.2.1.10 Lonza Group
    • 7.2.2 CRO Vendors
      • 7.2.2.1 CMIC Holdings Co. Ltd
      • 7.2.2.2 Covance Inc.
      • 7.2.2.3 Syneos Health Inc.
      • 7.2.2.4 LSK Global Pharma Service Co Ltd.
      • 7.2.2.5 Novotech Pty Ltd.
      • 7.2.2.6 PAREXEL International Corporation
      • 7.2.2.7 Pharmaceutical Product Development LLC
      • 7.2.2.8 PRA Health Sciences Inc.
      • 7.2.2.9 Quanticate Ltd.
      • 7.2.2.10 IQVIA Holdings Inc.
      • 7.2.2.11 SGS SA (SGS Life Sciences)
      • 7.2.2.12 Hangzhou Tigermed Consulting Co Ltd.
      • 7.2.2.13 Samsung Bioepis Co. Ltd.
      • 7.2.2.14 WuXi AppTec Inc.
      • 7.2.2.15 Sagimet Biosciences (3V Biosciences Inc.)

8 INVESTMENT ANALYSIS

9 MARKET OPPORTUNITIES AND FUTURE TRENDS