오믹스 기반 임상시험 시장 - 세계 산업 규모, 점유율, 동향, 기회, 예측, 단계별, 연구 디자인별, 적응증별, 지역별 부문, 경쟁(2020-2030년)

Omics-Based Clinical Trials Market - Global Industry Size, Share, Trends, Opportunity, and Forecast, Segmented By Phase, By Study Design, By Indication, By Region & Competition, 2020-2030F

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한글목차

오믹스 기반 임상시험 세계 시장 규모는 2024년 266억 7,000만 달러로 평가되었고, 예측 기간 동안 큰 폭으로 성장할 것으로 예상되며, 2030년까지 연평균 성장률(CAGR)은 7.25%를 나타낼 것으로 예상됩니다.

오믹스 기반 임상시험임상 연구에 참여하는 환자로부터 상세한 분자 데이터를 수집하기 위해 첨단 오믹스 기술을 통합합니다. 오믹스에는 생물학 및 의학에서 생체 분자를 분자 수준에서 분석하는 데 사용되는 다양한 고처리량 기술이 포함됩니다. 이러한 기술에는 유전체학(유전자와 DNA 연구), 단백질체학(단백질 연구), 대사체학(저분자 및 대사체 연구), 전사체학(RNA 및 유전자 발현 연구) 등이 포함됩니다. 오믹스 기반 임상시험의 주요 목적은 분자 프로파일을 기반으로 환자를 하위 그룹으로 세분화하여 보다 타겟팅된 맞춤형 의료 개입을 가능하게 하는 것입니다.

시장 개요
예측 기간	2026-2030년
시장 규모 : 2024년	266억 7,000만 달러
시장 규모 : 2030년	402억 6,000만 달러
CAGR : 2025-2030년	7.25%
급성장 부문	중재 연구
최대 시장	북미

그러나 오믹스 기반 임상시험은 데이터 표준화, 재현성 문제, 고도의 바이오인포매틱스 기능의 필요성 등의 과제에 직면해 있습니다. 성공적인 임상시험을 위해서는 오믹스 데이터의 정확성과 신뢰성이 매우 중요합니다. 예를 들어, 2024년 4월에 발표된 논문에서는 대사기능장애에 따른 지방간질환(MASLD) 관리에 있어 오믹스 기반 바이오마커의 중요성이 증가하고 있음을 강조하고 있습니다. 오믹스 기반 임상시험의 채택이 증가함에 따라 시장 성장이 더욱 촉진될 것으로 예상됩니다.

주요 시장 성장 촉진요인:

오믹스 기술의 발전

주요 시장 과제:

샘플 크기와 다양성

주요 시장 동향 :

멀티오믹스 데이터 통합

목차

제1장 개요

제2장 조사 방법

제3장 주요 요약

제4장 고객의 소리

제5장 세계의 오믹스 기반 임상시험 시장 전망

• 시장 규모와 예측
  • 금액별
• 시장 점유율과 예측
  • 단계별(단계 I, 단계 II, 단계 III, 단계 IV)
  • 연구 디자인별(확장된 접근 연구, 중개 연구, 관찰 연구)
  • 적응증별(심장병, 중추신경계 질환, 유전성 질환, 면역학, 종양학, 호흡기 질환, 피부 질환)
  • 지역별
  • 기업별(2024년)
• 시장 맵

제6장 아시아태평양의 오믹스 기반 임상시험 시장 전망

• 시장 규모와 예측
• 시장 점유율과 예측
• 아시아태평양 : 국가별 분석
  • 인도
  • 호주
  • 일본
  • 한국

제7장 유럽의 오믹스 기반 임상시험 시장 전망

• 시장 규모와 예측
• 시장 점유율과 예측
• 유럽 : 국가별 분석
  • 독일
  • 스페인
  • 이탈리아
  • 영국

제8장 북미의 오믹스 기반 임상시험 시장 전망

• 시장 규모와 예측
• 시장 점유율과 예측
• 북미 : 국가별 분석
  • 멕시코
  • 캐나다

제9장 남미의 오믹스 기반 임상시험 시장 전망

• 시장 규모와 예측
• 시장 점유율과 예측
• 남미 : 국가별 분석
  • 아르헨티나
  • 콜롬비아

제10장 중동 및 아프리카의 오믹스 기반 임상시험 시장 전망

• 시장 규모와 예측
• 시장 점유율과 예측
• 중동 및 아프리카 : 국가별 분석
  • 사우디아라비아
  • 아랍에미리트(UAE)

제11장 시장 역학

• 성장 촉진요인
• 과제

제12장 시장 동향과 발전

• 최근 동향
• 제품 출시
• 인수합병(M&A)

제13장 세계의 오믹스 기반 임상시험 시장 : SWOT 분석

제14장 Porter의 Five Forces 분석

• 업계내 경쟁
• 신규 참여 가능성
• 공급업체의 힘
• 고객의 힘
• 대체품의 위협

제15장 PESTEL 분석

제16장 경쟁 구도

• Parexel International Corporation
• Pharmaceutical Product Development(PPD)
• Charles River Laboratory
• ICON plc
• SGS SA
• Eli Lilly and Company
• Pfizer Inc.
• Covance Inc.
• Novo Nordisk
• Rebus Bio

제17장 전략적 제안

제18장 리서치사에 대해 & 면책사항

LSH

영문 목차

영문목차

The global Omics-Based Clinical Trials Market was valued at USD 26.67 billion in 2024 and is projected to experience substantial growth during the forecast period, with a compound annual growth rate (CAGR) of 7.25% through 2030. Omics-based clinical trials integrate advanced omics technologies to collect detailed molecular data from patients participating in clinical studies. Omics encompasses a range of high-throughput techniques used in biology and medicine to analyze biological molecules at the molecular level. These techniques include genomics (the study of genes and DNA), proteomics (the study of proteins), metabolomics (the study of small molecules and metabolites), transcriptomics (the study of RNA and gene expression), and more. A key objective of omics-based clinical trials is to stratify patients into subgroups based on their molecular profiles, enabling more targeted and personalized healthcare interventions.

Market Overview
Forecast Period	2026-2030
Market Size 2024	USD 26.67 Billion
Market Size 2030	USD 40.26 Billion
CAGR 2025-2030	7.25%
Fastest Growing Segment	Interventional Studies
Largest Market	North America

However, omics-based clinical trials face challenges such as data standardization, reproducibility issues, and the need for advanced bioinformatics capabilities. The accuracy and reliability of omics data are crucial for successful trials. For example, an article published in April 2024 highlights the growing significance of omics-based biomarkers in managing metabolic dysfunction-associated steatotic liver disease (MASLD), where these biomarkers aid in risk stratification and identifying patients with advanced fibrosis who are at higher risk of adverse outcomes. The increasing adoption of omics-based clinical trials is expected to further propel market growth.

Key Market Drivers:

Advancements in Omics Technologies

Recent developments in high-throughput sequencing have made these techniques faster, more precise, and cost-effective. Technologies like single-cell sequencing enable the examination of genetic material at an individual cell level, revealing cellular heterogeneity. Mass spectrometry tools have become more sensitive and precise, allowing the identification and quantification of proteins and metabolites in complex biological samples. Additionally, advancements in mass spectrometry imaging (MSI) enable the spatial mapping of molecules within tissues. Cryo-electron microscopy (cryo-EM) has revolutionized the structural analysis of proteins, achieving near-atomic resolution. X-ray crystallography and nuclear magnetic resonance (NMR) spectroscopy continue to enhance molecular structure resolution. Technologies such as stable isotope labeling and flux analysis offer insights into metabolic pathways, while quantitative proteomics methods, including isobaric labeling and label-free approaches, allow precise protein quantification.

A report from the Mayo Clinic in February 2023 highlights a new approach in genomics research, shifting some omics studies from traditional settings like hospitals to individuals' homes, particularly in rural and underserved areas. This change is expected to improve access to clinical trials, expanding participant pools and enabling more diverse data collection.

Key Market Challenges:

Sample Size and Diversity

One of the challenges of omics-based clinical trials is obtaining an adequate number of patient samples, particularly for rare diseases or genetically specific subpopulations. The availability of diverse patient samples is crucial, as these trials often require large and varied cohorts to generate reliable results. Biological variability among patients within the same disease category can be substantial, making it necessary to include larger sample sizes for statistical validity. Furthermore, ensuring genetic and ethnic diversity in clinical trial populations is essential for the broader applicability of findings. Omics-based trials often involve subgroup analysis based on genetic or molecular characteristics, and recruiting patients that meet these specific criteria can be time-consuming and resource-intensive. Delays in recruitment and data collection can hinder the trial process. Additionally, obtaining informed consent for genetic and molecular profiling, as well as addressing privacy concerns, can also present challenges.

The integration and interpretation of large, complex omics data sets also require advanced bioinformatics tools, which can further complicate the analysis, especially when dealing with large and diverse sample sizes.

Key Market Trends:

Integration of Multi-Omics Data

Different omics technologies provide unique perspectives on the molecular mechanisms underlying diseases. Integrating data from multiple omics disciplines offers a more comprehensive view of disease processes by examining the interplay of genes, proteins, metabolites, and other factors. This integration enhances the identification and validation of biomarkers for disease diagnosis, prognosis, and treatment response. Combining genetic, proteomic, and metabolic profiles leads to more accurate and robust biomarker discovery.

The integration of multi-omics data is pivotal for patient stratification, allowing researchers to classify patients based on molecular profiles and design more targeted clinical trials. This approach also facilitates the development of personalized therapies tailored to individual genetic, proteomic, and metabolic characteristics, leading to more effective treatments. In drug development, multi-omics integration helps to understand how drugs interact with various molecular components, providing insights into potential adverse effects and guiding drug design. For complex diseases like cancer, multi-omics data integration aids in understanding intricate molecular interactions, facilitating the identification of novel therapeutic targets and strategies. This integration aligns with a systems biology approach, offering a holistic understanding of biological systems as interconnected networks of genes, proteins, and metabolites.

Key Market Players:

• Parexel International Corporation
• Pharmaceutical Product Development (PPD)
• Charles River Laboratory
• ICON plc
• SGS SA
• Eli Lilly and Company
• Pfizer Inc.
• Covance Inc.
• Novo Nordisk
• Rebus Bio

Report Scope:

This report segments the global omics-based clinical trials market into various categories and provides a comprehensive analysis of market trends:

By Phase:

• Phase I
• Phase II
• Phase III
• Phase IV

By Study Design:

• Expanded Access Studies
• Interventional Studies
• Observational Studies

By Indication:

• Cardiology
• CNS Diseases
• Genetic Diseases
• Immunology
• Oncology
• Respiratory Diseases
• Skin Diseases

By Region:

• North America: United States, Canada, Mexico
• Asia-Pacific: China, India, South Korea, Australia, Japan
• Europe: Germany, France, United Kingdom, Spain, Italy
• South America: Brazil, Argentina, Colombia
• Middle East & Africa: South Africa, Saudi Arabia, UAE

Competitive Landscape:

This section provides detailed analysis and profiles of the major players in the global omics-based clinical trials market.

Available Customizations:

TechSci Research offers tailored customization options for this market report. These include a detailed analysis of additional market players (up to five) as per specific company needs.

Table of Contents

1. Product Overview

• 1.1. Market Definition
• 1.2. Scope of the Market
  • 1.2.1. Markets Covered
  • 1.2.2. Years Considered for Study
  • 1.2.3. Key Market Segmentations

2. Research Methodology

• 2.1. Objective of the Study
• 2.2. Baseline Methodology
• 2.3. Key Industry Partners
• 2.4. Major Association and Secondary Sources
• 2.5. Forecasting Methodology
• 2.6. Data Triangulation & Validation
• 2.7. Assumptions and Limitations

3. Executive Summary

• 3.1. Overview of the Market
• 3.2. Overview of Key Market Segmentations
• 3.3. Overview of Key Market Players
• 3.4. Overview of Key Regions/Countries
• 3.5. Overview of Market Drivers, Challenges, Trends

4. Voice of Customer

5. Global Omics-Based Clinical Trials Market Outlook

• 5.1. Market Size & Forecast
  • 5.1.1. By Value
• 5.2. Market Share & Forecast
  • 5.2.1. By Phase (Phase I, Phase II, Phase III, and Phase IV.)
  • 5.2.2. By Study Design (Expanded Access Studies, Interventional Studies, and Observational Studies)
  • 5.2.3. By Indication (Cardiology, CNS Diseases, Genetic Diseases, Immunology, Oncology, Respiratory Diseases, and Skin Diseases)
  • 5.2.4. By Region
  • 5.2.5. By Company (2024)
• 5.3. Market Map

6. Asia Pacific Omics-Based Clinical Trials Market Outlook

• 6.1. Market Size & Forecast
  • 6.1.1. By Value
• 6.2. Market Share & Forecast
  • 6.2.1. By Phase
  • 6.2.2. By Study Design
  • 6.2.3. By Indication
  • 6.2.4. By Country
• 6.3. Asia Pacific: Country Analysis
  • 6.3.1. China Omics-Based Clinical Trials Market Outlook
    • 6.3.1.1. Market Size & Forecast
      • 6.3.1.1.1. By Value
    • 6.3.1.2. Market Share & Forecast
      • 6.3.1.2.1. By Phase
      • 6.3.1.2.2. By Study Design
      • 6.3.1.2.3. By Indication
  • 6.3.2. India Omics-Based Clinical Trials Market Outlook
    • 6.3.2.1. Market Size & Forecast
      • 6.3.2.1.1. By Value
    • 6.3.2.2. Market Share & Forecast
      • 6.3.2.2.1. By Phase
      • 6.3.2.2.2. By Study Design
      • 6.3.2.2.3. By Indication
  • 6.3.3. Australia Omics-Based Clinical Trials Market Outlook
    • 6.3.3.1. Market Size & Forecast
      • 6.3.3.1.1. By Value
    • 6.3.3.2. Market Share & Forecast
      • 6.3.3.2.1. By Phase
      • 6.3.3.2.2. By Study Design
      • 6.3.3.2.3. By Indication
  • 6.3.4. Japan Omics-Based Clinical Trials Market Outlook
    • 6.3.4.1. Market Size & Forecast
      • 6.3.4.1.1. By Value
    • 6.3.4.2. Market Share & Forecast
      • 6.3.4.2.1. By Phase
      • 6.3.4.2.2. By Study Design
      • 6.3.4.2.3. By Indication
  • 6.3.5. South Korea Omics-Based Clinical Trials Market Outlook
    • 6.3.5.1. Market Size & Forecast
      • 6.3.5.1.1. By Value
    • 6.3.5.2. Market Share & Forecast
      • 6.3.5.2.1. By Phase
      • 6.3.5.2.2. By Study Design
      • 6.3.5.2.3. By Indication

7. Europe Omics-Based Clinical Trials Market Outlook

• 7.1. Market Size & Forecast
  • 7.1.1. By Value
• 7.2. Market Share & Forecast
  • 7.2.1. By Phase
  • 7.2.2. By Study Design
  • 7.2.3. By Indication
  • 7.2.4. By Country
• 7.3. Europe: Country Analysis
  • 7.3.1. France Omics-Based Clinical Trials Market Outlook
    • 7.3.1.1. Market Size & Forecast
      • 7.3.1.1.1. By Value
    • 7.3.1.2. Market Share & Forecast
      • 7.3.1.2.1. By Phase
      • 7.3.1.2.2. By Study Design
      • 7.3.1.2.3. By Indication
  • 7.3.2. Germany Omics-Based Clinical Trials Market Outlook
    • 7.3.2.1. Market Size & Forecast
      • 7.3.2.1.1. By Value
    • 7.3.2.2. Market Share & Forecast
      • 7.3.2.2.1. By Phase
      • 7.3.2.2.2. By Study Design
      • 7.3.2.2.3. By Indication
  • 7.3.3. Spain Omics-Based Clinical Trials Market Outlook
    • 7.3.3.1. Market Size & Forecast
      • 7.3.3.1.1. By Value
    • 7.3.3.2. Market Share & Forecast
      • 7.3.3.2.1. By Phase
      • 7.3.3.2.2. By Study Design
      • 7.3.3.2.3. By Indication
  • 7.3.4. Italy Omics-Based Clinical Trials Market Outlook
    • 7.3.4.1. Market Size & Forecast
      • 7.3.4.1.1. By Value
    • 7.3.4.2. Market Share & Forecast
      • 7.3.4.2.1. By Phase
      • 7.3.4.2.2. By Study Design
      • 7.3.4.2.3. By Indication
  • 7.3.5. United Kingdom Omics-Based Clinical Trials Market Outlook
    • 7.3.5.1. Market Size & Forecast
      • 7.3.5.1.1. By Value
    • 7.3.5.2. Market Share & Forecast
      • 7.3.5.2.1. By Phase
      • 7.3.5.2.2. By Study Design
      • 7.3.5.2.3. By Indication

8. North America Omics-Based Clinical Trials Market Outlook

• 8.1. Market Size & Forecast
  • 8.1.1. By Value
• 8.2. Market Share & Forecast
  • 8.2.1. By Phase
  • 8.2.2. By Study Design
  • 8.2.3. By Indication
  • 8.2.4. By Country
• 8.3. North America: Country Analysis
  • 8.3.1. United States Omics-Based Clinical Trials Market Outlook
    • 8.3.1.1. Market Size & Forecast
      • 8.3.1.1.1. By Value
    • 8.3.1.2. Market Share & Forecast
      • 8.3.1.2.1. By Phase
      • 8.3.1.2.2. By Study Design
      • 8.3.1.2.3. By Indication
  • 8.3.2. Mexico Omics-Based Clinical Trials Market Outlook
    • 8.3.2.1. Market Size & Forecast
      • 8.3.2.1.1. By Value
    • 8.3.2.2. Market Share & Forecast
      • 8.3.2.2.1. By Phase
      • 8.3.2.2.2. By Study Design
      • 8.3.2.2.3. By Indication
  • 8.3.3. Canada Omics-Based Clinical Trials Market Outlook
    • 8.3.3.1. Market Size & Forecast
      • 8.3.3.1.1. By Value
    • 8.3.3.2. Market Share & Forecast
      • 8.3.3.2.1. By Phase
      • 8.3.3.2.2. By Study Design
      • 8.3.3.2.3. By Indication

9. South America Omics-Based Clinical Trials Market Outlook

• 9.1. Market Size & Forecast
  • 9.1.1. By Value
• 9.2. Market Share & Forecast
  • 9.2.1. By Phase
  • 9.2.2. By Study Design
  • 9.2.3. By Indication
  • 9.2.4. By Country
• 9.3. South America: Country Analysis
  • 9.3.1. Brazil Omics-Based Clinical Trials Market Outlook
    • 9.3.1.1. Market Size & Forecast
      • 9.3.1.1.1. By Value
    • 9.3.1.2. Market Share & Forecast
      • 9.3.1.2.1. By Phase
      • 9.3.1.2.2. By Study Design
      • 9.3.1.2.3. By Indication
  • 9.3.2. Argentina Omics-Based Clinical Trials Market Outlook
    • 9.3.2.1. Market Size & Forecast
      • 9.3.2.1.1. By Value
    • 9.3.2.2. Market Share & Forecast
      • 9.3.2.2.1. By Phase
      • 9.3.2.2.2. By Study Design
      • 9.3.2.2.3. By Indication
  • 9.3.3. Colombia Omics-Based Clinical Trials Market Outlook
    • 9.3.3.1. Market Size & Forecast
      • 9.3.3.1.1. By Value
    • 9.3.3.2. Market Share & Forecast
      • 9.3.3.2.1. By Phase
      • 9.3.3.2.2. By Study Design
      • 9.3.3.2.3. By Indication

10. Middle East and Africa Omics-Based Clinical Trials Market Outlook

• 10.1. Market Size & Forecast
  • 10.1.1. By Value
• 10.2. Market Share & Forecast
  • 10.2.1. By Phase
  • 10.2.2. By Study Design
  • 10.2.3. By Indication
  • 10.2.4. By Country
• 10.3. MEA: Country Analysis
  • 10.3.1. South Africa Omics-Based Clinical Trials Market Outlook
    • 10.3.1.1. Market Size & Forecast
      • 10.3.1.1.1. By Value
    • 10.3.1.2. Market Share & Forecast
      • 10.3.1.2.1. By Phase
      • 10.3.1.2.2. By Study Design
      • 10.3.1.2.3. By Indication
  • 10.3.2. Saudi Arabia Omics-Based Clinical Trials Market Outlook
    • 10.3.2.1. Market Size & Forecast
      • 10.3.2.1.1. By Value
    • 10.3.2.2. Market Share & Forecast
      • 10.3.2.2.1. By Phase
      • 10.3.2.2.2. By Study Design
      • 10.3.2.2.3. By Indication
  • 10.3.3. UAE Omics-Based Clinical Trials Market Outlook
    • 10.3.3.1. Market Size & Forecast
      • 10.3.3.1.1. By Value
    • 10.3.3.2. Market Share & Forecast
      • 10.3.3.2.1. By Phase
      • 10.3.3.2.2. By Study Design
      • 10.3.3.2.3. By Indication

11. Market Dynamics

• 11.1. Drivers
• 11.2. Challenges

12. Market Trends & Developments

• 12.1. Recent Developments
• 12.2. Product Launches
• 12.3. Mergers & Acquisitions

13. Global Omics-Based Clinical Trials Market: SWOT Analysis

14. Porter's Five Forces Analysis

• 14.1. Competition in the Industry
• 14.2. Potential of New Entrants
• 14.3. Power of Suppliers
• 14.4. Power of Customers
• 14.5. Threat of Substitute Product

15. PESTLE Analysis

16. Competitive Landscape

• 16.1. Parexel International Corporation
  • 16.1.1. Business Overview
  • 16.1.2. Company Snapshot
  • 16.1.3. Products & Services
  • 16.1.4. Financials (In case of listed companies)
  • 16.1.5. Recent Developments
  • 16.1.6. SWOT Analysis
• 16.2. Pharmaceutical Product Development (PPD)
  • 16.2.1. Business Overview
  • 16.2.2. Company Snapshot
  • 16.2.3. Products & Services
  • 16.2.4. Financials (In case of listed companies)
  • 16.2.5. Recent Developments
  • 16.2.6. SWOT Analysis
• 16.3. Charles River Laboratory
  • 16.3.1. Business Overview
  • 16.3.2. Company Snapshot
  • 16.3.3. Products & Services
  • 16.3.4. Financials (In case of listed companies)
  • 16.3.5. Recent Developments
  • 16.3.6. SWOT Analysis
• 16.4. ICON plc
  • 16.4.1. Business Overview
  • 16.4.2. Company Snapshot
  • 16.4.3. Products & Services
  • 16.4.4. Financials (In case of listed companies)
  • 16.4.5. Recent Developments
  • 16.4.6. SWOT Analysis
• 16.5. SGS SA
  • 16.5.1. Business Overview
  • 16.5.2. Company Snapshot
  • 16.5.3. Products & Services
  • 16.5.4. Financials (In case of listed companies)
  • 16.5.5. Recent Developments
  • 16.5.6. SWOT Analysis
• 16.6. Eli Lilly and Company
  • 16.6.1. Business Overview
  • 16.6.2. Company Snapshot
  • 16.6.3. Products & Services
  • 16.6.4. Financials (In case of listed companies)
  • 16.6.5. Recent Developments
  • 16.6.6. SWOT Analysis
• 16.7. Pfizer Inc.
  • 16.7.1. Business Overview
  • 16.7.2. Company Snapshot
  • 16.7.3. Products & Services
  • 16.7.4. Financials (In case of listed companies)
  • 16.7.5. Recent Developments
  • 16.7.6. SWOT Analysis
• 16.8. Covance Inc.
  • 16.8.1. Business Overview
  • 16.8.2. Company Snapshot
  • 16.8.3. Products & Services
  • 16.8.4. Financials (In case of listed companies)
  • 16.8.5. Recent Developments
  • 16.8.6. SWOT Analysis
• 16.9. Novo Nordisk
  • 16.9.1. Business Overview
  • 16.9.2. Company Snapshot
  • 16.9.3. Products & Services
  • 16.9.4. Financials (In case of listed companies)
  • 16.9.5. Recent Developments
  • 16.9.6. SWOT Analysis
• 16.10.Rebus Bio
  • 16.10.1. Business Overview
  • 16.10.2. Company Snapshot
  • 16.10.3. Products & Services
  • 16.10.4. Financials (In case of listed companies)
  • 16.10.5. Recent Developments
  • 16.10.6. SWOT Analysis

17. Strategic Recommendations

18. About Us & Disclaimer

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