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Global Investigational New Drug CDMO Market (2021 to 2028) - Featuring Catalent, Lonza and Patheon Among Others - ResearchAndMarkets.com

Global Investigational New Drug CDMO Market (2021 to 2028) - Featuring Catalent, Lonza and Patheon Among Others - ResearchAndMarkets.com

全球研究新药CDMO市场(2021至2028)-以Catalent、Lonza和Patheon等公司为特色-reearchandmarket s.com
Businesswire ·  2021/11/02 09:20

DUBLIN--(BUSINESS WIRE)--The "Investigational New Drug CDMO Market Size, Share & Trends Analysis Report By Product (Small Molecule, Large Molecule), By Service (Contract Development, Contract Manufacturing), By End User, And Segment Forecasts, 2021 - 2028" report has been added to ResearchAndMarkets.com's offering.

都柏林--(美国商业新闻网)--“2021-2028年研究新药CDMO市场规模、份额和趋势分析报告(按产品(小分子、大分子)、按服务(合同开发、合同制造)、按最终用户和细分预测)”报告已被添加到Research andMarkets.com的献祭。


The global investigational new drug CDMO market size is expected to reach USD 6.8 billion by 2028, according to a new report by the publisher It is expected to expand at a CAGR of 6.9% from 2021 to 2028.

根据出版商的一份新报告,到2028年,全球研究新药CDMO的市场规模预计将达到68亿美元,预计2021年至2028年将以6.9%的复合年增长率增长。

Companies Mentioned

提到的公司

  • Catalent, Inc.
  • Lonza
  • Recipharm AB
  • Siegfried Holding AG
  • Patheon Inc.
  • Covance
  • IQVIA Holdings Inc.
  • Cambrex Corporation
  • Charles River Laboratories International, Inc.
  • Syneous Health
  • Catalent,Inc.
  • 龙沙
  • Recipharm AB
  • 齐格弗里德控股公司
  • Patheon Inc.
  • Covance
  • IQVIA控股公司
  • Cambrex公司
  • 查尔斯·里弗国际实验室公司
  • Syneous Health

The U.S. FDA and the European Medicines Agency (EMA) are health authority bodies that regulate the use of investigational drugs in the U.S. and the European Union, respectively. In addition, investigational review boards (IRBs) in the U.S. and ethics committees (ECs) in the European Union must approve the use of drugs in humans.

美国食品和药物管理局(FDA)和欧洲药品管理局(EMA)是卫生权威机构,分别在美国和欧盟监管研究药物的使用。此外,美国的调查审查委员会(IRBs)和欧盟的伦理委员会(ECs)必须批准在人体上使用药物。

It is the requirement of a federal law that a drug be the subject of an approved marketing application prior to it is distributed or transported across the state lines. Hence, sponsors aiming to conduct clinical studies that involve an IND should gain exemption from the FDA to permit the shipping of the investigational drug to clinical investigators in several states.

联邦法律要求一种药物在跨州分销或运输之前,必须成为批准的上市申请的对象。因此,旨在进行涉及IND的临床研究的赞助商应该获得FDA的豁免,以允许将研究药物运送到几个州的临床研究人员手中。

The pandemic has significantly impacted the global economy in 2020 and has an ongoing impact on various industries. However, the market for IND CDMO has benefited from the pandemic. Prior to COVID-19, prospective sponsors demanded facility audits to ensure CDMOs had the required capacity, equipment, and personnel to undertake their projects. Nowadays, CDMOs should find new ways to attract new sponsors, such as through videos, virtual reality, and other technologies that allow sponsors to virtually experience the site.

这场大流行对2020年的全球经济产生了重大影响,并对各个行业产生了持续的影响。然而,IND CDMO的市场已经从这场大流行中受益。在新冠肺炎之前,潜在的赞助商要求对设施进行审计,以确保CDMO拥有开展项目所需的能力、设备和人员。如今,CDMO应该寻找新的方式来吸引新的赞助商,比如通过视频、虚拟现实和其他允许赞助商虚拟体验网站的技术。

Investigational New Drug CDMO Market Report Highlights

正在研究的新药CDMO市场报告要点

  • In terms of product, the small molecule segment dominated the market with a revenue share of 89.0% in 2020. This is largely due to the increasing number of small molecules in development. Besides, in 2019, the small molecules dominated the new drug approvals accounting for 79% of all the NME approvals
  • Based on service, the contract development segment led the market with a revenue share of 85.5% in 2020. The contract development offers several benefits over in-house development of drugs, such as access to industry experts, less time to market, cost-effectiveness, and more focus on core competencies
  • By end user, pharmaceutical companies accounted for the largest share of 69.4% in 2020. This is due to the changes in the pharmaceutical industry that have an impact on research and development strategies, which, in turn, influence new drug approval trends
  • Asia Pacific to register the fastest growth rate of 7.7% over the forecast period. Due to the rapid growth of pharmaceutical firms and contract manufacturing organizations in developing countries, such as India and China, the region is likely to overtake Europe and North America in the near future
  • 从产品来看,2020年,小分子细分市场以89.0%的营收份额占据主导地位。这在很大程度上是由于正在开发的小分子数量不断增加。此外,2019年,小分子药物主导了新药批准,占所有NME批准的79%
  • 基于服务,合同开发细分市场在2020年以85.5%的收入份额领先市场。与内部药物开发相比,合同开发提供了几个好处,例如可以接触到行业专家、更少的上市时间、成本效益以及更多地关注核心能力。
  • 按终端用户划分,2020年药企占比最大,为69.4%。这是由于制药行业的变化对研发战略产生了影响,而研发战略反过来又影响了新药审批趋势。
  • 亚太地区将在预测期内录得7.7%的最快增长率。由于印度和中国等发展中国家的制药公司和代工组织的快速增长,该地区很可能在不久的将来超过欧洲和北美

Key Topics Covered:

涵盖的主要主题:

Chapter 1 Methodology and Scope

第一章方法和范围

Chapter 2 Executive Summary

第2章执行摘要

Chapter 3 Global IND CDMO Market: Variables, Trends, & Scope

第三章全球IND CDMO市场:变量、趋势和范围

3.1 Market Segmentation and Scope

3.1市场细分和范围

3.2 Market Dynamics

3.2市场动态

3.2.1 Market Driver Analysis

3.2.1市场驱动因素分析

3.2.1.1 Increasing outsourcing services by pharmaceutical companies

3.2.1.1增加制药公司的外包服务

3.2.1.2 Rising investment in R&D

3.2.1.2研发投入不断增加

3.2.1.3 Growing pharmaceutical industry

3.2.1.3成长中的制药业

3.2.1.5 Stringent regulatory requirements

3.2.1.5严格的监管要求

3.2.2 Market Restraint Analysis

3.2.2市场约束分析

3.2.2.1 Compliance issues while outsourcing

3.2.2.1外包时的合规问题

3.2.2.2 Changing scenario in developing countries

3.2.2.2发展中国家不断变化的情景

3.3 Penetration & Growth Prospect Mapping

3.3渗透率和增长前景图

3.4 COVID-19 Impact on the Market

3.4.新冠肺炎对市场的影响

3.5 Major Deals and Strategic Alliances Analysis

3.5主要交易和战略联盟分析

3.6 Global IND CDMO: Market Analysis Tools

3.6全球Ind CDMO:市场分析工具

3.6.1 Industry Analysis - Porter's

3.6.1行业分析-波特的

3.6.3 PESTEL Analysis

3.6.3柔和分析

Chapter 4 Global IND CDMO Market: Product Segment Analysis

第四章全球IND CDMO市场:产品细分分析

Chapter 5 Global IND CDMO Market: Service Segment Analysis

第五章全球IND CDMO市场:服务细分分析

Chapter 6 Global IND CDMO Market: End-user Segment Analysis

第六章全球IND CDMO市场:终端用户细分分析

Chapter 7 Global IND CDMO Market: Regional Analysis

第七章全球IND CDMO市场:区域分析

Chapter 8 Company Profiles

第八章公司概况

For more information about this report visit https://www.researchandmarkets.com/r/gsvvj4

有关本报告的更多信息,请访问https://www.researchandmarkets.com/r/gsvvj4。


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