Clinical Trial Supply & Logistics Market

Global Clinical Trial Supply & Logistics Market Report: By Phase (Phase I, Phase II, Phase III, and Phase IV) By Service (Logistics & Distribution, Storage & Retention Packaging, Labelling, And Blinding, Manufacturing, Comparator Sourcing, and Other Services), and Region (North America, Europe, Asia-Pacific, Latin America, Middle-East and Africa) Global Industry Analysis, Size, Share, Growth, Trends, Regional Analysis, Competitor Analysis and Forecast 2023-2031.

Medical Devices | January 2024 | Report ID: EMR00451 | Pages: 301

Global Clinical Trial Supply & Logistics market is predicted to reach approximately USD 6.35 billion by 2031, at a CAGR of 7.12% from 2022 to 2031.

The market for global clinical trial supply and logistics includes the complex web of procedures and activities that go into organising, locating, producing, labelling, packing, and distributing investigational medicinal products (IMPs) for clinical trials. Prior to being introduced to the general public, these trials are essential for assessing the efficacy and safety of novel medications, biologics, and medical devices. The primary goal of the market is to guarantee the prompt and effective delivery of trial materials to different clinical trial sites across the globe while complying with strict regulatory standards and preserving the trial process' integrity.

This dynamic market is driven by the rising complexity of clinical trials, globalization of research and development activities, and the increasing focus on precision medicine and personalized therapies. Key stakeholders in the Clinical Trial Supply & Logistics market include pharmaceutical and biotechnology companies, contract research organizations (CROs), clinical trial supply providers, and logistics partners. The industry grapples with challenges such as stringent regulatory compliance, temperature-sensitive trial materials, and the need for seamless communication and coordination among diverse stakeholders.

 

 

Global Clinical Trial Supply & Logistics report scope and segmentation.

Report Attribute

Details

Estimated Market Value (2022)

USD 3.42 billion

Projected Market Value (2031)

USD 6.35 billion

Base Year

2022

Forecast Years

2023 – 2031

Scope of the Report

Historical and Forecast Trends, Industry Drivers and Constraints, Historical and Forecast Market Analysis by Segment- Based on By Phase, Therapeutic Area, Service, End-use & Region.

Segments Covered

By Phase, Therapeutic Area, Service, End-use & By Region.

Forecast Units

Value (USD Billion or Million), and Volume (Units)

Quantitative Units

Revenue in USD million/billion and CAGR from 2023 to 2031.

Regions Covered

North America, Europe, Asia Pacific, Latin America, and Middle East & Africa.

Countries Covered

U.S., Canada, Mexico, U.K., Germany, France, Italy, Spain, China, India, Japan, South Korea, Brazil, Argentina, GCC Countries, and South Africa, among others.

Report Coverage

Market growth drivers, restraints, opportunities, Porter’s five forces analysis, PEST analysis, value chain analysis, regulatory landscape, market attractiveness analysis by segments and region, company market share analysis.

Delivery Format

Delivered as an attached PDF and Excel through email, according to the purchase option.

 

Global Clinical Trial Supply & Logistics dynamics

The ongoing advancements in biotechnology and pharmaceutical research are a major factor contributing to the rise in intricate clinical trials. Agile and effective supply chain solutions are needed as the industry struggles to meet the rising demand for personalised therapies and precision medicine. Furthermore, companies are conducting research in various geographic locations to increase patient diversity and shorten trial timelines, a trend known as the globalisation of clinical trials. Although there are more opportunities due to this trend, navigating the regulatory maze, cultural differences, and disparate infrastructures requires strong logistics and supply strategies.

Regulatory compliance remains a critical aspect influencing market dynamics, as the industry is subject to stringent guidelines governing the handling, transportation, and documentation of clinical trial materials. The increasing focus on patient-centric trials and decentralized clinical trials is reshaping the landscape, driving the need for flexible and patient-friendly supply chain solutions. The market is also witnessing advancements in technology adoption, with blockchain, real-time tracking systems, and data analytics playing pivotal roles in optimizing supply chain visibility and mitigating risks.

 

Global Clinical Trial Supply & Logistics drivers

  • Increasing Complexity of Clinical Trials

A sophisticated infrastructure for Clinical Trial Supply & Logistics is required due to the increasing complexity of clinical trials resulting from ongoing advancements in pharmaceutical and biotechnology research. The increasing complexity of clinical trials, coupled with an emphasis on tailored treatments and precision medicine, is driving up demand for effective supply chains and specialised logistics. The market is driven forward by this complexity driver, which encourages the adoption of innovative technologies like real-time tracking systems and predictive analytics to guarantee the timely and smooth delivery of investigational medicinal products (IMPs) to various global trial sites.

  • Globalization of Clinical Trials

The trend towards conducting clinical trials on a global scale presents a significant driver for the Clinical Trial Supply & Logistics market. Pharmaceutical and biotechnology companies are increasingly seeking to enhance patient diversity, accelerate trial timelines, and access broader patient populations. However, this globalization introduces challenges related to navigating diverse regulatory landscapes, cultural variations, and infrastructural differences. Companies are compelled to develop robust supply chain strategies, including temperature-controlled transportation and adherence to complex international regulations, driving the demand for specialized logistics services and fostering collaborations between industry participants.

 

Restraints:

  • Stringent Regulatory Compliance

Strict regulations controlling the handling, transportation, and documentation of clinical trial materials pose a significant obstacle to the market for clinical trial supply and logistics. The logistics processes become more complex due to the need to comply with a variety of constantly changing international regulations, which necessitates careful attention to detail and copious documentation. Significant delays, monetary fines, and, in extreme circumstances, the integrity of clinical trials may be jeopardised by non-compliance. For industry stakeholders, navigating this complicated regulatory environment is a never-ending challenge.

  • Challenges in Patient-Centric and Decentralized Trials

The industry is experiencing a shift towards patient-centric and decentralized clinical trials, driven by the need for greater patient participation and reduced burden. While these approaches offer advantages, they pose challenges for supply chain logistics. Delivering trial materials directly to patients' homes or diverse locations requires innovative solutions to ensure product integrity, maintain regulatory compliance, and address the unique needs of each trial participant. The complexities introduced by patient-centric and decentralized trials serve as a restraint, demanding adaptability and tailored logistics strategies.

 

Opportunities:

  • Technological Advancements

For market participants, the continuous technological developments in the Clinical Trial Supply & Logistics sector offer a sizable opportunity. Blockchain, Internet of Things (IoT), and artificial intelligence are examples of innovations that improve supply chain visibility and risk mitigation by enabling real-time tracking, temperature monitoring, and predictive analytics. Adopting these technologies can give businesses a competitive edge in the market by streamlining processes, cutting expenses, and increasing overall efficiency.

 

Segment Overview

  • By Phase

The segmentation based on clinical trial phases comprises Phase I, Phase II, Phase III, and Phase IV. Each phase represents a distinct stage in the drug development process, with unique logistical and supply chain requirements. Phase I focuses on initial safety testing, Phase II on efficacy and side effects, Phase III on expanded efficacy and monitoring, and Phase IV involves post-marketing surveillance. Tailoring logistics solutions to the specific demands of each phase is essential for the successful execution of clinical trials.

  • By Application  

The application-based segmentation encompasses logistics & distribution, storage & retention, packaging, labelling, and blinding, manufacturing, comparator sourcing, and other services. These applications collectively address the diverse operational aspects of clinical trial supply and logistics, ranging from the efficient and secure transportation of investigational materials to the manufacturing and labelling processes crucial for maintaining compliance and product integrity throughout the trial.

  • By Therapeutic Area

The therapeutic area segmentation includes Oncology, Cardiovascular Diseases, Respiratory Diseases, CNS and Mental Disorders, and Others. Each therapeutic area presents unique challenges and considerations in terms of clinical trial supply chain logistics. For example, oncology trials often involve complex and specialized treatments, requiring meticulous planning for the timely and secure delivery of investigational drugs to various global trial sites.

  • By End-use

The end-use segmentation involves pharmaceuticals, biologicals, and medical devices. This categorization reflects the diverse nature of clinical trial products, including traditional pharmaceuticals, biologics such as vaccines and gene therapies, and medical devices requiring specific handling and distribution considerations. Different end-use industries demand tailored logistics solutions to accommodate the distinctive characteristics of their products and adhere to regulatory requirements.

 

Global Clinical Trial Supply & Logistics Overview by Region

North America, particularly the United States, stands as a key player in the market, driven by a robust pharmaceutical industry, advanced healthcare systems, and a high prevalence of clinical trials. Europe follows closely, with countries like the United Kingdom and Germany contributing significantly to the market's growth, supported by a well-established research ecosystem and adherence to stringent regulatory standards. The Asia-Pacific region is emerging as a substantial player, propelled by a growing emphasis on clinical research, a large patient pool, and a favourable regulatory environment in countries like China and India.

Latin America and the Middle East & Africa regions are experiencing increased attention, driven by the globalization of clinical trials and efforts to enhance patient diversity. However, these regions face challenges related to infrastructure development, regulatory harmonization, and economic factors. The global COVID-19 pandemic has also influenced regional dynamics, with disruptions in clinical trial timelines and supply chains, emphasizing the need for adaptable strategies.

 

 

Global Clinical Trial Supply & Logistics market competitive landscape

Prominent pharmaceutical companies, Contract Research Organizations (CROs), and specialized logistics providers contribute to a dynamic and multifaceted competitive environment. Companies such as Catalent, Inc., Fisher Clinical Services, and Marken, a UPS Company, are recognized for their extensive capabilities in clinical trial supply chain management, encompassing logistics, packaging, labeling, and distribution.

Strategic collaborations and partnerships play a pivotal role in enhancing the competitive standing of industry participants. These collaborations often involve the integration of technology and innovative solutions to address evolving challenges in the clinical trial landscape. Moreover, mergers and acquisitions are prevalent strategies among key players seeking to broaden their service offerings, expand global reach, and strengthen their position in the market. As an example, acquisitions of specialized logistics companies by larger pharmaceutical service providers contribute to a more integrated and streamlined supply chain.

 

Global Clinical Trial Supply & Logistics Recent Developments

  • June 2023, SkyCell, a pioneering and primary producer of temperature-controlled hybrid containers designed for the pharmaceutical sector, has joined forces with Marken to offer cutting-edge shipping solutions for pharmaceutical products involved in clinical trials. Through this partnership, Marken will have access to SkyCell containers, ensuring the secure transportation of critical and temperature-sensitive drugs.
  • Feb 2022, ZS, a prominent global professional services firm, revealed today that it is forging a strategic partnership with IgniteData, a digital health startup based in the U.K. ZS is making a significant multimillion-dollar investment in IgniteData, which is known for its Archer technology, contributing to the advancement of clinical research in the digital health space.

 

Scope of global Clinical Trial Supply & Logistics report

Global Clinical Trial Supply & Logistics report segmentation

ATTRIBUTE

DETAILS

By Phase

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

By Application

  • Logistics & Distribution
  • Storage & Retention
  • Packaging, Labeling, And Blinding
  • Manufacturing
  • Comparator Sourcing
  • Other Services

By Therapeutic Area

  • Oncology
  • Cardiovascular Diseases
  • Respiratory Diseases
  • CNS And Mental Disorders
  • Others

By End-use

  • Pharmaceuticals
  • Biologicals
  • Medical Devices

By Geography

  • North America (USA, and Canada)
  • Europe (UK, Germany, France, Italy, Spain, Russia and Rest of Europe)
  • Asia Pacific (Japan, China, India, Australia, Southeast Asia and Rest of Asia Pacific)
  • Latin America (Brazil, Mexico, and Rest of Latin America)
  • Middle East & Africa (South Africa, GCC, and Rest of Middle East & Africa)

Customization Scope

  • Available upon request

Pricing

  • Available upon request

 

Objectives of the Study

The objectives of the study are summarized in 5 stages. They are as mentioned below:

  • Global Clinical Trial Supply & Logistics size and forecast: To identify and estimate the market size for global Clinical Trial Supply & Logistics market segmented by Phase, Therapeutic Area, Service, End-use and by region. Also, to understand the consumption/ demand created by consumers between 2023 and 2031.
  • Market Landscape and Trends: To identify and infer the drivers, restraints, opportunities, and challenges for global Clinical Trial Supply & Logistics
  • Market Influencing Factors: To find out the factors which are affecting the market of global Clinical Trial Supply & Logistics among consumers.
  • Company Profiling: To provide a detailed insight into the major companies operating in the market. The profiling will include the financial health of the company's past 2-3 years with segmental and regional revenue breakup, product offering, recent developments, SWOT analysis, and key strategies.

Research Methodology

Our research methodology has always been the key differentiating reason which sets us apart in comparison from the competing organizations in the industry. Our organization believes in consistency along with quality and establishing a new level with every new report we generate; our methods are acclaimed and the data/information inside the report is coveted. Our research methodology involves a combination of primary and secondary research methods. Data procurement is one of the most extensive stages in our research process. Our organization helps in assisting the clients to find the opportunities by examining the market across the globe coupled with providing economic statistics for each and every region.  The reports generated and published are based on primary & secondary research. In secondary research, we gather data for global Market through white papers, case studies, blogs, reference customers, news, articles, press releases, white papers, and research studies. We also have our paid data applications which includes hoovers, Bloomberg business week, Avention, and others.

Data Collection

Data collection is the process of gathering, measuring, and analyzing accurate and relevant data from a variety of sources to analyze market and forecast trends. Raw market data is obtained on a broad front. Data is continuously extracted and filtered to ensure only validated and authenticated sources are considered. Data is mined from a varied host of sources including secondary and primary sources.

Primary Research

After the secondary research process, we initiate the primary research phase in which we interact with companies operating within the market space. We interact with related industries to understand the factors that can drive or hamper a market. Exhaustive primary interviews are conducted. Various sources from both the supply and demand sides are interviewed to obtain qualitative and quantitative information for a report which includes suppliers, product providers, domain experts, CEOs, vice presidents, marketing & sales directors, Type & innovation directors, and related key executives from various key companies to ensure a holistic and unbiased picture of the market. 

Secondary Research

A secondary research process is conducted to identify and collect information useful for the extensive, technical, market-oriented, and comprehensive study of the market. Secondary sources include published market studies, competitive information, white papers, analyst reports, government agencies, industry and trade associations, media sources, chambers of commerce, newsletters, trade publications, magazines, Bloomberg BusinessWeek, Factiva, D&B, annual reports, company house documents, investor presentations, articles, journals, blogs, and SEC filings of companies, newspapers, and so on. We have assigned weights to these parameters and quantified their market impacts using the weighted average analysis to derive the expected market growth rate.

Top-Down Approach & Bottom-Up Approach

In the top – down approach, the Global Batteries for Solar Energy Storage Market was further divided into various segments on the basis of the percentage share of each segment. This approach helped in arriving at the market size of each segment globally. The segments market size was further broken down in the regional market size of each segment and sub-segments. The sub-segments were further broken down to country level market. The market size arrived using this approach was then crosschecked with the market size arrived by using bottom-up approach.

In the bottom-up approach, we arrived at the country market size by identifying the revenues and market shares of the key market players. The country market sizes then were added up to arrive at regional market size of the decorated apparel, which eventually added up to arrive at global market size.

This is one of the most reliable methods as the information is directly obtained from the key players in the market and is based on the primary interviews from the key opinion leaders associated with the firms considered in the research. Furthermore, the data obtained from the company sources and the primary respondents was validated through secondary sources including government publications and Bloomberg.

Market Analysis & size Estimation

Post the data mining stage, we gather our findings and analyze them, filtering out relevant insights. These are evaluated across research teams and industry experts. All this data is collected and evaluated by our analysts. The key players in the industry or markets are identified through extensive primary and secondary research. All percentage share splits, and breakdowns have been determined using secondary sources and verified through primary sources. The market size, in terms of value and volume, is determined through primary and secondary research processes, and forecasting models including the time series model, econometric model, judgmental forecasting model, the Delphi method, among Flywheel Energy Storage. Gathered information for market analysis, competitive landscape, growth trends, product development, and pricing trends is fed into the model and analyzed simultaneously.

Quality Checking & Final Review

The analysis done by the research team is further reviewed to check for the accuracy of the data provided to ensure the clients’ requirements. This approach provides essential checks and balances which facilitate the production of quality data. This Type of revision was done in two phases for the authenticity of the data and negligible errors in the report. After quality checking, the report is reviewed to look after the presentation, Type and to recheck if all the requirements of the clients were addressed.

Frequently Asked Questions

Global Clinical Trial Supply & Logistics forecast period is 2023 - 2031.
According to global Clinical Trial Supply & Logistics research, the market is expected to grow at a CAGR of ~7.12% over the next eight years.
The possible segments in global Clinical Trial Supply & Logistics are based on by Phase, Therapeutic Area, Service, End-use & by region.
The expected market size for Global Clinical Trial Supply & Logistics is USD 3.42 billion in 2022.
The major players in the market are Catalent, Inc., DHL, FedEx, Marken, Movianto, Parexel, Packaging Coordinators Inc., Piramal Pharma Solutions, Thermo Fisher Scientific (Patheon), UDG Healthcare, and Almac Group.