Clinical Trial Supplies Market By Share, Size and Forecast 2028

Summary

Report Description

The global clinical trial supplies market is anticipated to observe impressive growth during the forecast period, 2024-2028, owing to the growing number of registered clinical trials. Factors such as increased research and development activities, globalization of clinical trials, complexity of study designs, and stringent regulatory requirements have risen the demand for clinical trial supplies in the market.

Clinical trials are an essential component of the drug development process, enabling researchers and pharmaceutical companies to evaluate the safety and efficacy of new treatments and therapies. As more innovative drugs and therapies enter the development pipeline, the need for adequate supplies to support these trials has significantly increased.

Growing Research & Development

A remarkable expansion in medical research and development activities can be observed across the world. With advancements in technology and an increasing understanding of complex diseases, there has been a surge in the number of clinical trials being conducted across various therapeutic areas, such as oncology, neurology, cardiology, and infectious diseases. According to the US National Library of Medicine's clinical data, a total of 68,272 studies are found for cardiology. As a result, the demand for trial supplies, including investigational drugs, medical devices, and diagnostic tools, has correspondingly risen.

Furthermore, the globalization of clinical trials has played a significant role in driving the demand for supplies. Pharmaceutical companies and research organizations are increasingly conducting trials in multiple countries to access diverse patient populations and gain regulatory approvals in various regions. This trend has created a need for clinical trial supplies to be distributed across different geographical locations, ensuring that each trial site has access to the necessary resources.

Increasing Advancement of Clinical Trials

Modern clinical trials often involve sophisticated protocols, innovative study designs, and personalized medicine approaches. These advancements require specialized supplies and technologies, such as biomarkers, genetic testing kits, specialized packaging, and temperature-controlled storage and transport systems. As a result, the demand for these specialized supplies has risen to accommodate the evolving needs of clinical trial designs. Modern clinical trials often involve complex study designs, such as adaptive trials, biomarker-driven trials, and personalized medicine approaches. Based on the clinical trial data by the US National Library of Medicine, 1,843 studies have been performed related to predictive markers. The demand for these specialized supplies has grown as researchers strive to capture more accurate and comprehensive data during clinical trials.

Rising Regulatory Requirements to Ensure Patient Safety

Moreover, regulatory requirements have become more stringent to ensure patient safety and data integrity in clinical trials. Regulatory authorities, such as the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA), have implemented rigorous guidelines for the storage, handling, and documentation of clinical trial supplies. The European Medicines Agency (EMA) focuses its decisions about the approval of medicines on the findings of clinical trials conducted by pharmaceutical companies. Although clinical trials in the European Union (EU) are authorized at the national level, EMA is crucial as cutting-edge clinical trials and to the maintenance of IT systems for the coordination of clinical trials. This has led to an increased demand for supplies that meet regulatory compliance, such as Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP). Pharmaceutical companies and contract research organizations (CROs) must source high-quality supplies that adhere to these standards, further driving the demand for clinical trial materials.

Regulatory authorities have implemented increasingly rigorous guidelines to ensure patient safety, data integrity, and compliance in clinical trials. Pharmaceutical companies and contract research organizations (CROs) ensure they obtain high-quality supplies that meet regulatory standards.

To meet the growing demand for clinical trial supplies, various stakeholders in the pharmaceutical industry have ramped up their manufacturing capabilities and supply chain infrastructure. Pharmaceutical companies, CROs, and specialized suppliers are expanding their production capacities, enhancing their logistics capabilities, and optimizing their distribution networks. Additionally, advancements in digital technologies, such as supply chain management systems and real-time tracking, have improved the efficiency and traceability of clinical trial supplies.

Growing Number of Clinical Trials

Clinical trials are crucial for advancing medical knowledge, evaluating new treatments and therapies, and improving patient care. The rising number of registered trials reflects the growing interest in medical research, the development of innovative therapies, and the recognition of the importance of evidence-based medicine. According to the United States National Library of Medicine, there are currently a total of 452,604 studies registered in Clinicaltrials.gov, with locations in all 50 states and 221 countries around the globe. One of the primary reasons for the increased number of registered clinical trials is the rapid advancement of medical science and technology. The discovery of new disease targets, improved understanding of molecular mechanisms, and breakthroughs in areas like genomics, immunology, and regenerative medicine have opened new avenues for research. This has generated a surge in the development of novel therapies and interventions, leading to a greater need for clinical trials to evaluate their safety and effectiveness.

Additionally, there is a growing awareness among healthcare professionals, researchers, and the public about the importance of evidence-based medicine. Clinical trials provide a rigorous and systematic approach to evaluate the efficacy and safety of medical interventions. As the demand for evidence-based medicine continues to rise, more researchers and institutions are conducting clinical trials to generate high-quality data that can guide medical decision-making and improve patient outcomes. Furthermore, the globalization of clinical research has also contributed to the increased number of registered trials. In the past, clinical trials were predominantly conducted in developed countries. However, there has been a significant shift towards conducting trials in diverse geographic locations, including emerging markets and developing countries. According to clinicaltrials.gov, as of May 17, 2023, the total number of Registered Studies is 140,268, whereas in recent times there are around 240,844 registered studies in non-US locations. This expansion is driven by several factors, such as access to larger patient populations, diverse genetic backgrounds, reduced costs, and expedited regulatory pathways. As a result, there has been a proliferation of clinical trials being registered in regions that were previously understated in medical research.

Rising Demand for Biologics

Advances in biotechnology have revolutionized the development of biologics. These therapies, including monoclonal antibodies, recombinant proteins, cell and gene therapies, and vaccines, offer innovative treatment options for a wide range of diseases, including cancer, autoimmune disorders, and rare genetic conditions. The unique nature of biologics necessitates extensive testing and evaluation through clinical trials, leading to an increased demand for clinical trial supplies.

Biologics are typically produced using complex manufacturing processes involving living cells or organisms. These processes require specialized facilities, equipment, and expertise to ensure the safety, efficacy, and quality of the final product. Clinical trials involving biologics require adequate supplies of these specialized manufacturing materials, including cell lines, culture media, growth factors, vectors, and other components essential for the production of biologic therapies.

Download Free Sample Report

Regulatory authorities have established rigorous standards for the approval of biologics due to their complex nature and potential impact on patient health. The demand for clinical trial supplies arises from the need to conduct well-designed trials that comply with regulatory guidelines and generate robust evidence for regulatory submissions. Biologic therapies often target specific patient populations, such as those with rare diseases or specific genetic profiles. Clinical trials involving these therapies require careful patient selection and enrollment processes to ensure the evaluation of treatment effectiveness in the targeted population.

Additionally, biologics are frequently used in combination therapies or personalized medicine approaches, where multiple therapies or treatment regimens are tailored to individual patients. Clinical trials investigating these complex treatment modalities require a comprehensive supply of various biologic agents, diagnostic tools, and supporting supplies to ensure accurate dosing, monitoring, and safety assessments.

Moreover, the rise of biosimilars, which are highly similar versions of already approved biologic therapies, has also contributed to the increased demand for clinical trial supplies. Biosimilars require clinical trials to establish similarity in terms of safety, efficacy, and quality compared to the reference biologic. These trials necessitate adequate supplies of both the biosimilar and the reference product for comparative evaluations.

Market Segmentation:

The global clinical trial supplies market can be segmented based on services, type, therapeutic areas, end user, region and competitive landscape. Based on services, the market can be categorized into manufacturing, packaging, labeling & blinding, logistics & distribution, storage & retention, comparator sourcing, and others. Based on type, the market is segmented into small molecule drugs, biologic drugs, and medical devices. Based on therapeutic areas, the market can be fragmented into oncology, CNS and mental disorders, cardiovascular diseases, digestive disorders, infectious diseases, metabolic disorders, blood disorders, immunology, and other therapeutic disorders. Based on end user, the market is segmented into pharmaceutical companies, biotechnology companies, and Contract Research Organizations (CROs). Based on region, the market is segmented into North America, Europe, Asia-Pacific, South America, and the Middle East & Africa.

Market Players

Thermo Fisher Scientific Inc., Catalent Inc, Almac Group, PRA Health Sciences, Piramal Pharma Solutions, Clinigen Group Plc, Eurofins Scientific SE, Parexel International Corporation, are some of the key players operating in the Global Clinical Trial Supplies Market.

Attribute	Details
Base Year	2022
Historic Data	2018 – 2021
Estimated Year	2023
Forecast Period	2024 – 2028
Quantitative Units	Revenue in USD Million, and CAGR for 2018-2022 and 2023-2028
Report coverage	Revenue forecast, company share, competitive landscape, growth factors, and trends
Segments covered	By Services By Type By Therapeutic Areas By End User
Regional scope	North America; Europe; Asia Pacific; South America; Middle East & Africa
Country scope	United States; Canada; Mexico; Germany; France; United Kingdom; Spain; Italy; China; India; Japan; South Korea; Australia; Brazil; Argentina; Colombia; South Africa; UAE; Saudi Arabia
Key companies profiled	Thermo Fisher Scientific Inc., Catalent Inc, Almac Group, Pra Health Sciences, Piramal Pharma Solutions, Clinigen Group Plc, Eurofins Scientific SE, Parexel International Corporation
Customization scope	10% free report customization with purchase. Addition or alteration to country, regional & segment scope.
Pricing and purchase options	Avail customized purchase options to meet your exact research needs. Explore purchase options
Delivery Format	PDF and Excel through Email (We can also provide the editable version of the report in PPT/Word format on special request)

Report Scope:

In this report, Global Clinical Trial Supplies Market has been segmented into following categories, in addition to the industry trends which have also been detailed below:

Clinical Trial Supplies Market, By Services:

Manufacturing
Packaging Labeling & Blinding
Logistics & Distribution
Storage & Retention
Comparator Sourcing
Other

Clinical Trial Supplies, By Type:

Small Molecule drugs
Biologics drugs
Medical Devices

Clinical Trial Supplies, By Therapeutic Areas:

Oncology
CNS and Mental Disorders
Cardiovascular diseases
Digestive disorders
Infectious Diseases
Metabolic disorders
Blood disorders
Immunology
Other therapeutic disorder

Clinical Trial Supplies, By End User:

Pharmaceutical
Biotechnology companies
Contract Research Organizations (CROs)

Clinical Trial Supplies, By Region:

North America

United States
Canada
Mexico

Europe

Germany
France
United Kingdom
Italy
Spain

Asia-Pacific

China
Japan
India
South Korea
Australia

South America

Brazil
Argentina
Colombia

Middle East & Africa

UAE
Saudi Arabia
South Africa

Competitive Landscape

Company Profiles: Detailed analysis of the major companies present in Global Clinical Trial Supplies Market.

Available Customizations:

With the given Market data, TechSci Research offers customizations according to a company’s specific needs. The following customization options are available for the report:

Company Information

Detailed analysis and profiling of additional Market players (up to five).

It is an upcoming report to be released soon. If you wish an early delivery of this report or want to confirm the date of release, please contact us at [email protected]

Table of content

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. Global Clinical Trial Supplies Market Outlook

4.1. Market Size & Forecast

4.1.1. By Value

4.2. Market Share & Forecast

4.2.1. By Services (Manufacturing, Packaging Labeling & Blinding, Logistics & Distribution, Storage & Retention, Comparator Sourcing, Other)

4.2.2. By Type (Small Molecule drugs, Biologics drugs, Medical Devices)

4.2.3. By Therapeutic Areas (Oncology, CNS and Mental Disorders Cardiovascular diseases, Digestive disorders, Infectious Diseases, Metabolic disorders, Blood disorders, Immunology, and other therapeutic disorder)

4.2.4. By End User (Pharmaceutical, Biotechnology Companies, Contract Research Organizations (CROs))

4.2.5. By Region (North America, Europe, Asia Pacific, South America, Middle East & Africa)

4.2.6. By Company (2022)

4.3. Market Map

5. North America Clinical Trial Supplies Market Outlook

5.1. Market Size & Forecast

5.1.1. By Value

5.2. Market Share & Forecast

5.2.1. By Services

5.2.2. By Type

5.2.3. By Therapeutic Areas

5.2.4. By End User

5.2.5. By Country

5.3. North America: Country Analysis

5.3.1. United States Clinical Trial Supplies Market Outlook

5.3.1.1. Market Size & Forecast

5.3.1.1.1. By Value

5.3.1.2. Market Share & Forecast

5.3.1.2.1. By Services

5.3.1.2.2. By Type

5.3.1.2.3. By Therapeutic Areas

5.3.1.2.4. By End User

5.3.2. Canada Clinical Trial Supplies Market Outlook

5.3.2.1. Market Size & Forecast

5.3.2.1.1. By Value

5.3.2.2. Market Share & Forecast

5.3.2.2.1. By Services

5.3.2.2.2. By Type

5.3.2.2.3. By Therapeutic Areas

5.3.2.2.4. By End User

5.3.3. Mexico Clinical Trial Supplies Market Outlook

5.3.3.1. Market Size & Forecast

5.3.3.1.1. By Value

5.3.3.2. Market Share & Forecast

5.3.3.2.1. By Services

5.3.3.2.2. By Type

5.3.3.2.3. By Therapeutic Areas

5.3.3.2.4. By End User

6. Europe Clinical Trial Supplies Market Outlook

6.1. Market Size & Forecast

6.1.1. By Value

6.2. Market Share & Forecast

6.2.1. By Services

6.2.2. By Type

6.2.3. By Therapeutic Areas

6.2.4. By End User

6.2.5. By Country

6.3. Europe: Country Analysis

6.3.1. Germany Clinical Trial Supplies 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 Services

6.3.1.2.2. By Type

6.3.1.2.3. By Therapeutic Areas

6.3.1.2.4. By End User

6.3.2. France Clinical Trial Supplies 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 Services

6.3.2.2.2. By Type

6.3.2.2.3. By Therapeutic Areas

6.3.2.2.4. By End User

6.3.3. United Kingdom Clinical Trial Supplies 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 Services

6.3.3.2.2. By Type

6.3.3.2.3. By Therapeutic Areas

6.3.3.2.4. By End User

6.3.4. Italy Clinical Trial Supplies 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 Services

6.3.4.2.2. By Type

6.3.4.2.3. By Therapeutic Areas

6.3.4.2.4. By End User

6.3.5. Spain Clinical Trial Supplies 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 Services

6.3.5.2.2. By Type

6.3.5.2.3. By Therapeutic Areas

6.3.5.2.4. By End User

7. Asia-Pacific Clinical Trial Supplies Market Outlook

7.1. Market Size & Forecast

7.1.1. By Value

7.2. Market Share & Forecast

7.2.1. By Services

7.2.2. By Type

7.2.3. By Therapeutic Areas

7.2.4. By End User

7.2.5. By Country

7.3. Asia-Pacific: Country Analysis

7.3.1. China Clinical Trial Supplies 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 Services

7.3.1.2.2. By Type

7.3.1.2.3. By Therapeutic Areas

7.3.1.2.4. By End User

7.3.2. Japan Clinical Trial Supplies 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 Services

7.3.2.2.2. By Type

7.3.2.2.3. By Therapeutic Areas

7.3.2.2.4. By End User

7.3.3. India Clinical Trial Supplies 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 Services

7.3.3.2.2. By Type

7.3.3.2.3. By Therapeutic Areas

7.3.3.2.4. By End User

7.3.4. South Korea Clinical Trial Supplies 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 Services

7.3.4.2.2. By Type

7.3.4.2.3. By Therapeutic Areas

7.3.4.2.4. By End User

7.3.5. Australia Clinical Trial Supplies 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 Services

7.3.5.2.2. By Type

7.3.5.2.3. By Therapeutic Areas

7.3.5.2.4. By End User

8. South America Clinical Trial Supplies Market Outlook

8.1. Market Size & Forecast

8.1.1. By Value

8.2. Market Share & Forecast

8.2.1. By Services

8.2.2. By Type

8.2.3. By Therapeutic Areas

8.2.4. By End User

8.2.5. By Country

8.3. South America: Country Analysis

8.3.1. Brazil Clinical Trial Supplies 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 Services

8.3.1.2.2. By Type

8.3.1.2.3. By Therapeutic Areas

8.3.1.2.4. By End User

8.3.2. Argentina Clinical Trial Supplies 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 Services

8.3.2.2.2. By Type

8.3.2.2.3. By Therapeutic Areas

8.3.2.2.4. By End User

8.3.3. Colombia Clinical Trial Supplies 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 Services

8.3.3.2.2. By Type

8.3.3.2.3. By Therapeutic Areas

8.3.3.2.4. By End User

9. Middle East and Africa Clinical Trial Supplies Market Outlook

9.1. Market Size & Forecast

9.1.1. By Value

9.2. Market Share & Forecast

9.2.1. By Services

9.2.2. By Type

9.2.3. By Therapeutic Areas

9.2.4. By End User

9.2.5. By Country

9.3. MEA: Country Analysis

9.3.1. UAE Clinical Trial Supplies 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 Services

9.3.1.2.2. By Type

9.3.1.2.3. By Therapeutic Areas

9.3.1.2.4. By End User

9.3.2. Saudi Arabia Clinical Trial Supplies 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 Services

9.3.2.2.2. By Type

9.3.2.2.3. By Therapeutic Areas

9.3.2.2.4. By End User

9.3.3. South Africa Clinical Trial Supplies 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 Services

9.3.3.2.2. By Type

9.3.3.2.3. By Therapeutic Areas

9.3.3.2.4. By End User

10. Market Dynamics

10.1. Drivers

10.2. Challenges

11. Market Trends & Developments

12. Competitive Landscape

12.1. Business Overview

12.2. Product Offerings

12.3. Recent Developments

12.4. Financials (In Case of Listed Companies)

12.5. Key Personnel

12.5.1. THERMO FISHER SCIENTIFIC INC.

12.5.2. CATALENT INC

12.5.3. ALMAC GROUP

12.5.4. PRA HEALTH SCIENCES

12.5.5. PIRAMAL PHARMA SOLUTIONS

12.5.6. CLINIGEN GROUP PLC

12.5.7. EUROFINS SCIENTIFIC SE

12.5.8. PAREXEL INTERNATIONAL CORPORATION

Strategic Recommendations

Figures and Tables

Frequently asked questions

What will be the scenario of Global Clinical Trial Supplies Market in 2028?

Global Clinical Trial Supplies Market is expected to grow at an impressive rate on account of the increasing number of registered clinical trials. Also, rising research and development activities, globalization of clinical trials and complexity of study designs and stringent regulatory requirements are factors propelling market demand.

Which region is expected to dominate the Global Clinical Trial Supplies Market in the forecast period?

Asia Pacific holds the highest share in the market in 2022 and is expected to dominate the market in the forecast period due to growing government investment & support for clinical trials. Also, rising research & development, a large patient pool, and low operating cost to launch a clinical trial, etc. are some factors that are boosting the Global Clinical Trial Supplies Market in the Asia- Pacific region.

Who are the key players operating in Global Clinical Trial Supplies Market?

Thermo Fisher Scientific Inc., Catalent Inc, Almac Group, Pra Health Sciences, Piramal Pharma Solutions, Clinigen Group Plc, Eurofins Scientific SE, Parexel International Corporation, among others are some of the leading players operating in the Global Clinical Trial Supplies Market.

What factors are restricting the growth of Global Clinical Trial Supplies Market?

The high cost of conduction of clinical trials is a major factor restraining the growth of the Global Clinical Trial Supplies Market during the forecast period.

Related Reports

Sakshi Bajaal

Business Consultant

Talk To Analyst

Press Release

Clinical Trial Supplies Market to be dominated by Oncology Segment through 2028

Sep, 2023

Rising research & development of innovative drugs and therapies is expected to drive the growth of Global Clinical Trial Supplies Market during the forecast period.

Buy Now