Bioequivalence Studies Market (By Molecule Type; By Dosage Form; By Therapeutic Area; By Study Type) - Global Industry Analysis, Size, Share, Growth, Trends, Revenue, Regional Outlook and Forecast 2022-2030

Industry Insights

The global market for bioequivalence studies is anticipated to register significant growth over the forecast period. The increasing manufacturing of generic drugs and the rising number of clinical trial studies for drug development are the main driving factors of the market, as they help spur the growth of bioequivalence studies, which are performed to form a link between the early and late clinical trial formulations. Furthermore, R&D investments made by various pharmaceutical and biopharmaceutical companies for disease prevention are expected to aid in market growth. 

The COVID-19 pandemic has greatly impacted our ability to conduct bioequivalence studies. Due to the pandemic, the government announced a "stay at home" order for the prevention of coronavirus, which led to various clinical trials being halted and delayed, study site closures, laboratory closures, and participant enrollment being postponed. However, bioequivalence studies will resume in the second half of 2020 in order to develop effective drugs for pandemic treatment and prevention. 

Based on therapeutic areas , oncology dominated the market. This is because cancer is the main cause of death, making it crucial to guarantee that patients have access to anticancer treatments in order to enhance their quality of life and lower hospital costs and mortality linked to the disease. Bioequivalence studies are thus carried out to investigate these drugs and this helps in the growth of the market. According to WHO, in 2020, cancer accounted for approximately 10 million deaths worldwide.

The North America region is anticipated to dominate the market over the forecast period. This is due to the presence of major market players offering bioequivalence Studies, the expansion of the healthcare infrastructure, and the increasing prevalence of disease, which will increase the demand for drugs that will in turn increase clinical trials for drug development, and the R&D expenditures made by market players for the creation of new treatments and this will help in the growth of bioequivalence studies required to check bioavailability and PK/PD parameters.

The key market players operating in this market are CliniExperts, ICBIO Corporation, ProRelix Services LLP, ICON plc, Charles River Laboratories International, PPD, Inc, Labcorp Drug Development, IQVIA, Syneos Health, SGS SA, and Intertek Group plc. They are adopting various strategies like partnership. collaboration, merger and acquisition, and expansion.

Market Segmentation

By Type Outlook

  • Small Molecule
  • Large Molecule

By Dosage Form Outlook

  • Solid Oral Dosage
  • Parenteral Formulations
  • Topical Products
  • Others

By Therapeutic Area Outlook

  • Oncology
  • Neurology
  • Metabolic Disorders
  • Hematology
  • Immunology
  • Orthopedics
  • Others

By Phase Outlook

  • Drug Discover
  • Preclinical Studies
  • Clinical Studies

By Regional Outlook

  • North America
  • Europe
  • Asia Pacific
  • Latin America
  • MEA

Chapter 1. Introduction

1.1. Research Objective

1.2. Scope of the Study

1.3. Definition

Chapter 2. Research Methodology

2.1. Research Approach

2.2. Data Sources

2.3. Assumptions & Limitations

Chapter 3. Executive Summary

3.1. Market Snapshot

Chapter 4. Market Variables and Scope 

4.1. Introduction

4.2. Market Classification and Scope

4.3. Industry Value Chain Analysis

4.3.1. Raw Material Procurement Analysis 

4.3.2. Sales and Distribution Channel Analysis

4.3.3. Downstream Buyer Analysis

Chapter 5. COVID 19 Impact on Bioequivalence Studies Market 

5.1. COVID-19 Landscape: Bioequivalence Studies Industry Impact

5.2. COVID 19 - Impact Assessment for the Industry

5.3. COVID 19 Impact: Global Major Government Policy

5.4. Market Trends and Opportunities in the COVID-19 Landscape

Chapter 6. Market Dynamics Analysis and Trends

6.1. Market Dynamics

6.1.1. Market Drivers

6.1.2. Market Restraints

6.1.3. Market Opportunities

6.2. Porter’s Five Forces Analysis

6.2.1. Bargaining power of suppliers

6.2.2. Bargaining power of buyers

6.2.3. Threat of substitute

6.2.4. Threat of new entrants

6.2.5. Degree of competition

Chapter 7. Competitive Landscape

7.1.1. Company Market Share/Positioning Analysis

7.1.2. Key Strategies Adopted by Players

7.1.3. Vendor Landscape

7.1.3.1. List of Suppliers

7.1.3.2. List of Buyers

Chapter 8. Global Bioequivalence Studies Market, By Type

8.1. Bioequivalence Studies Market, by Type, 2022-2030

8.1.1. Small Molecule

8.1.1.1. Market Revenue and Forecast (2017-2030)

8.1.2. Large Molecule

8.1.2.1. Market Revenue and Forecast (2017-2030)

Chapter 9. Global Bioequivalence Studies Market, By Dosage Form

9.1. Bioequivalence Studies Market, by Dosage Form, 2022-2030

9.1.1. Solid Oral Dosage

9.1.1.1. Market Revenue and Forecast (2017-2030)

9.1.2. Parenteral Formulations

9.1.2.1. Market Revenue and Forecast (2017-2030)

9.1.3. Topical Products

9.1.3.1. Market Revenue and Forecast (2017-2030)

9.1.4. Others

9.1.4.1. Market Revenue and Forecast (2017-2030)

Chapter 10. Global Bioequivalence Studies Market, By Therapeutic Area 

10.1. Bioequivalence Studies Market, by Therapeutic Area, 2022-2030

10.1.1. Oncology

10.1.1.1. Market Revenue and Forecast (2017-2030)

10.1.2. Neurology

10.1.2.1. Market Revenue and Forecast (2017-2030)

10.1.3. Metabolic Disorders

10.1.3.1. Market Revenue and Forecast (2017-2030)

10.1.4. Hematology

10.1.4.1. Market Revenue and Forecast (2017-2030)

10.1.5. Immunology

10.1.5.1. Market Revenue and Forecast (2017-2030)

10.1.6. Orthopedics

10.1.6.1. Market Revenue and Forecast (2017-2030)

10.1.7. Others

10.1.7.1. Market Revenue and Forecast (2017-2030)

Chapter 11. Global Bioequivalence Studies Market, By Phase 

11.1. Bioequivalence Studies Market, by Phase, 2022-2030

11.1.1. Drug Discover

11.1.1.1. Market Revenue and Forecast (2017-2030)

11.1.2. Preclinical Studies

11.1.2.1. Market Revenue and Forecast (2017-2030)

11.1.3. Clinical Studies

11.1.3.1. Market Revenue and Forecast (2017-2030)

Chapter 12. Global Bioequivalence Studies Market, Regional Estimates and Trend Forecast

12.1. North America

12.1.1. Market Revenue and Forecast, by Type (2017-2030)

12.1.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.1.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.1.4. Market Revenue and Forecast, by Phase (2017-2030)

12.1.5. U.S.

12.1.5.1. Market Revenue and Forecast, by Type (2017-2030)

12.1.5.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.1.5.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.1.5.4. Market Revenue and Forecast, by Phase (2017-2030)

12.1.6. Rest of North America

12.1.6.1. Market Revenue and Forecast, by Type (2017-2030)

12.1.6.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.1.6.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.1.6.4. Market Revenue and Forecast, by Phase (2017-2030)

12.2. Europe

12.2.1. Market Revenue and Forecast, by Type (2017-2030)

12.2.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.2.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.2.4. Market Revenue and Forecast, by Phase (2017-2030)

12.2.5. UK

12.2.5.1. Market Revenue and Forecast, by Type (2017-2030)

12.2.5.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.2.5.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.2.5.4. Market Revenue and Forecast, by Phase (2017-2030)

12.2.6. Germany

12.2.6.1. Market Revenue and Forecast, by Type (2017-2030)

12.2.6.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.2.6.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.2.6.4. Market Revenue and Forecast, by Phase (2017-2030)

12.2.7. France

12.2.7.1. Market Revenue and Forecast, by Type (2017-2030)

12.2.7.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.2.7.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.2.7.4. Market Revenue and Forecast, by Phase (2017-2030)

12.2.8. Rest of Europe

12.2.8.1. Market Revenue and Forecast, by Type (2017-2030)

12.2.8.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.2.8.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.2.8.4. Market Revenue and Forecast, by Phase (2017-2030)

12.3. APAC

12.3.1. Market Revenue and Forecast, by Type (2017-2030)

12.3.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.3.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.3.4. Market Revenue and Forecast, by Phase (2017-2030)

12.3.5. India

12.3.5.1. Market Revenue and Forecast, by Type (2017-2030)

12.3.5.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.3.5.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.3.5.4. Market Revenue and Forecast, by Phase (2017-2030)

12.3.6. China

12.3.6.1. Market Revenue and Forecast, by Type (2017-2030)

12.3.6.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.3.6.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.3.6.4. Market Revenue and Forecast, by Phase (2017-2030)

12.3.7. Japan

12.3.7.1. Market Revenue and Forecast, by Type (2017-2030)

12.3.7.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.3.7.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.3.7.4. Market Revenue and Forecast, by Phase (2017-2030)

12.3.8. Rest of APAC

12.3.8.1. Market Revenue and Forecast, by Type (2017-2030)

12.3.8.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.3.8.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.3.8.4. Market Revenue and Forecast, by Phase (2017-2030)

12.4. MEA

12.4.1. Market Revenue and Forecast, by Type (2017-2030)

12.4.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.4.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.4.4. Market Revenue and Forecast, by Phase (2017-2030)

12.4.5. GCC

12.4.5.1. Market Revenue and Forecast, by Type (2017-2030)

12.4.5.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.4.5.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.4.5.4. Market Revenue and Forecast, by Phase (2017-2030)

12.4.6. North Africa

12.4.6.1. Market Revenue and Forecast, by Type (2017-2030)

12.4.6.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.4.6.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.4.6.4. Market Revenue and Forecast, by Phase (2017-2030)

12.4.7. South Africa

12.4.7.1. Market Revenue and Forecast, by Type (2017-2030)

12.4.7.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.4.7.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.4.7.4. Market Revenue and Forecast, by Phase (2017-2030)

12.4.8. Rest of MEA

12.4.8.1. Market Revenue and Forecast, by Type (2017-2030)

12.4.8.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.4.8.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.4.8.4. Market Revenue and Forecast, by Phase (2017-2030)

12.5. Latin America

12.5.1. Market Revenue and Forecast, by Type (2017-2030)

12.5.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.5.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.5.4. Market Revenue and Forecast, by Phase (2017-2030)

12.5.5. Brazil

12.5.5.1. Market Revenue and Forecast, by Type (2017-2030)

12.5.5.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.5.5.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.5.5.4. Market Revenue and Forecast, by Phase (2017-2030)

12.5.6. Rest of LATAM

12.5.6.1. Market Revenue and Forecast, by Type (2017-2030)

12.5.6.2. Market Revenue and Forecast, by Dosage Form (2017-2030)

12.5.6.3. Market Revenue and Forecast, by Therapeutic Area (2017-2030)

12.5.6.4. Market Revenue and Forecast, by Phase (2017-2030)

Chapter 13. Company Profiles

13.1. CliniExperts

13.1.1. Company Overview

13.1.2. Product Offerings

13.1.3. Financial Performance

13.1.4. Recent Initiatives

13.2. ICBIO Corporation

13.2.1. Company Overview

13.2.2. Product Offerings

13.2.3. Financial Performance

13.2.4. Recent Initiatives

13.3. ProRelix Services LLP

13.3.1. Company Overview

13.3.2. Product Offerings

13.3.3. Financial Performance

13.3.4. Recent Initiatives

13.4. ICON plc

13.4.1. Company Overview

13.4.2. Product Offerings

13.4.3. Financial Performance

13.4.4. Recent Initiatives

13.5. Charles River Laboratories International

13.5.1. Company Overview

13.5.2. Product Offerings

13.5.3. Financial Performance

13.5.4. Recent Initiatives

13.6. PPD, Inc

13.6.1. Company Overview

13.6.2. Product Offerings

13.6.3. Financial Performance

13.6.4. Recent Initiatives

13.7. Labcorp Drug Development

13.7.1. Company Overview

13.7.2. Product Offerings

13.7.3. Financial Performance

13.7.4. Recent Initiatives

13.8. IQVIA

13.8.1. Company Overview

13.8.2. Product Offerings

13.8.3. Financial Performance

13.8.4. Recent Initiatives

13.9. Syneos Health

13.9.1. Company Overview

13.9.2. Product Offerings

13.9.3. Financial Performance

13.9.4. Recent Initiatives

13.10. SGS SA

13.10.1. Company Overview

13.10.2. Product Offerings

13.10.3. Financial Performance

13.10.4. Recent Initiatives

Chapter 14. Research Methodology

14.1. Primary Research

14.2. Secondary Research

14.3. Assumptions

Chapter 15. Appendix

15.1. About Us

15.2. Glossary of Terms

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