Clinical Trial Supplies

Clinical Trial Supplies Market by Phase (Phase I, Phase II, Phase III), Туре (Biologic Drugs, Medical Devices, Small-Molecules), Product, Therapeutic Area, End User - Global Forecast 2024-2030

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[184 Pages Report] The Clinical Trial Supplies Market size was estimated at USD 3.35 billion in 2023 and expected to reach USD 3.64 billion in 2024, at a CAGR 8.43% to reach USD 5.92 billion by 2030.

Clinical Trial Supplies Market
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Clinical trial supplies are a fundamental yet complex component of clinical research, ultimately helping pave the way toward successful therapeutic breakthroughs and monumental enhancements in patient care pathways. These supplies cater to various research phases, from pre-clinical examinations to post-marketing surveillance studies, thus facilitating the seamless management and execution of clinical investigations. The increasing prevalence of infectious and chronic diseases worldwide and the subsequent rise in clinical trials with research and development expenditure of the pharmaceutical and biopharmaceutical industry stimulates market growth. The high cost associated with clinical trial supplies, stringent regulations for supplies, and cross-border logistics challenges restrict market growth. Growing emphasis on drug development and shifting towards patient-centric clinical trials offer the potential for better clinical trial patient recruitment, study enrollment, and participant retention. In addition, ongoing advancements in a diverse range of clinical trial supplies are expected to open new research avenues for pharmaceutical and biopharmaceutical companies.

Clinical Trial Supplies Market - Global Forecast 2024-2030
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Phase: Growing demand for clinical trial supplies for each phase for optimal decision-making regarding clinical trial

Phase I trials, typically small-scale, evaluate new biomedical interventions for safety, dosage tolerance, and side effects. Phase II trials conduct a more extensive evaluation of safety and efficacy, and phase III trials, significantly larger in scope, monitor a drug's efficacy and adverse reactions amongst diverse populations. Phase IV trials occur post-drug approval, involving the monitoring of drug effectiveness, side effects, and the collation of long-term data. Clinical trials necessitate distinct deliverables in every phase, necessitating the selection of a supplier based on their specialization and up-to-date advancements. The selection of a supplier whose capabilities align with the requirements of each phase is crucial for the successful execution of trial operations. Researchers can ensure compliance with the demands of each clinical trial phase by considering supplier specializations and staying informed about recent developments.

Туре: Surge in biologic drugs demand with breakthrough therapies for chronic ailments

Biologic drugs, including vaccines, blood components, and allergens, offer solutions for chronic and life-threatening diseases. Recent advances in biotechnologies have led to an enhanced focus on biological drugs. Medical devices cover a broad spectrum, from surgical instruments to diagnostic machines. Small molecules include most drug therapy products, enabling various disorders, especially those with considerable patient populations. Biologic drugs have grown significantly with radical therapies for chronic diseases; medical devices are transformed by technological advancements emphasizing minimally invasive procedures. Meanwhile, small molecules continue a steady growth trend, thriving on introducing innovative treatments for widespread diseases.

Product: Auxiliary medicinal products are vital elements of clinical trials, owing to their significance of assuring safety, and efficiency in the overall research operation

Auxiliary medicinal products primarily include supplementary medications and supplements used to manage the side effects of primary treatment therapies. Interactive response technology (IRT) solutions facilitate randomized subject enrollment and drug supply management in clinical trials. Lab supplies form a critical segment of clinical trial supplies, with occasional increments per the scale of clinical trial activities. Clinical trials necessitate using various lab supplies, including centrifuges, microscopes, and pipettes. Centrifuges help in separating different components of a sample based on their densities. Microscopes are crucial for viewing specimens at a microscopic level. Pipettes, on the other hand, are used for measuring and transferring small volumes of liquids. Reagents are substances or mixtures used in chemical analysis or other reactions. In a clinical trial setting, reagents are pivotal in detecting, measuring, examining, or producing other substances.

Medical devices and diagnostics are central to clinical trials, as they ensure accuracy in measurements, monitoring, detection, or treatment of conditions or diseases. Pharmacy supplies encompass biohazard bags, compounding aseptic isolators, and sterilization equipment. Biohazard bags are used to dispose of waste that contains potentially infectious substances. Compounding aseptic isolators protect from exposure to airborne contaminants. Sterilization equipment is necessary to eradicate all forms of life and other biological agents from the materials used in the study. Research materials are fundamental to the trial's success, ranging from trial-specific medication to placebos and controlled substances. Safety equipment forms an essential part of any clinical trial and includes gloves, safety glasses, and lab coats, amongst others, to ensure the safety of all involved. Consequently, additional medicinal products are vital elements of clinical trials. Their significance lies in their ability to support the primary trial interventions while assuring safety, accuracy, and efficiency in the overall research operation.

Therapeutic Area: Rising burden of infectious diseases worldwide create a demand for clinical trial supplies

Cardiology refers to the diagnosis and treatment of diseases of the cardiovascular system, including the heart and blood vessels. Clinical supplies required for cardiology trials include various diagnostic tools such as echocardiograms, stress test equipment, and medications for heart conditions. Genetic diseases involve disorders caused by abnormalities in an individual's genetic material. Clinical trials in this sector necessitate technologies such as DNA sequencing and polymerase chain reaction (PCR) supplies. Immunology is concerned with the body's immune response to harmful pathogens. Clinical supplies here include reagents used for immunological assays, cytometers for cell analysis, and supplies for cell culture. Infectious diseases deal with diseases caused by organisms such as bacteria, viruses, fungi, or parasites. Supplies for clinical trials include microbiological culture supplies, antimicrobial agents, and advanced diagnostic kits. Metabolic disorders include conditions that disrupt normal metabolism, converting food to energy. Clinical supplies include blood glucose monitoring devices, insulin pens, pumps, or lipid-lowering drugs. Neurology is a field dedicated to the diagnosis and treatment of disorders affecting the nervous system; this sector utilizes neuroimaging tools, cognitive test supplies, and neurological biomarkers. Oncology involves the study of cancer, its treatments, and clinical trials. Clinical supplies range from chemotherapies and radiation therapies to developing new oncology drugs and therapeutic supplies.

End User: Growing use of clinical trial supplies in CROs due to rising outsourcing of R&D activities

Contract research organizations (CROs) are essential in clinical trial supplies by providing various services and spearheading innovative solutions to enhance drug development. These organizations offer the escalated complexity of clinical trials and increased outsourcing of research and development functions. Pharmaceutical and biotech manufacturers focus on maintaining high manufacturing standards, drug safety, and quality control. These companies have become indispensable by providing an intact chain of custody, ensuring product efficacy, and serving regulatory norms. CROs and pharmaceutical/biotech firms both hold quality and supply chain proficiency in high regard. While CROs seek flexible and innovative supply solutions, pharmaceutical and biotech firms lean towards stable manufacturing and robust safety protocols.

Regional Insights

In the Americas, primarily the United States and Canada, there is a significant dependence on clinical trial supplies due to a high diagnosis rate of chronic diseases and robust healthcare infrastructure. Over the past year, the major patents registered revolved around optimizing supply chain models and employing advanced analytics to align trial supply with demand. The European Union (EU), the Middle East, and Africa exhibit a diverse range of needs due to discrepancies in healthcare access and spending. Europe witnesses steady demand for clinical trial supplies, fueled by heavy investments in research and development initiatives and a surge in the geriatric population. In contrast, Middle Eastern and African countries encompass emerging markets with rising research activities yet laid back due to limited funding and infrastructural impediments. Asia-Pacific, including China, Japan, and India, reports a high disease prevalence, bridged by substantial investments in improving healthcare infrastructure. The booming pharmaceutical industry drives the clinical trial supplies market in these regions, and the demand is dictated more by cost-efficacy rather than speed, mirroring their unique healthcare economic dynamics.

FPNV Positioning Matrix

The FPNV Positioning Matrix is pivotal in evaluating the Clinical Trial Supplies Market. It offers a comprehensive assessment of vendors, examining key metrics related to Business Strategy and Product Satisfaction. This in-depth analysis empowers users to make well-informed decisions aligned with their requirements. Based on the evaluation, the vendors are then categorized into four distinct quadrants representing varying levels of success: Forefront (F), Pathfinder (P), Niche (N), or Vital (V).

Market Share Analysis

The Market Share Analysis is a comprehensive tool that provides an insightful and in-depth examination of the current state of vendors in the Clinical Trial Supplies Market. By meticulously comparing and analyzing vendor contributions in terms of overall revenue, customer base, and other key metrics, we can offer companies a greater understanding of their performance and the challenges they face when competing for market share. Additionally, this analysis provides valuable insights into the competitive nature of the sector, including factors such as accumulation, fragmentation dominance, and amalgamation traits observed over the base year period studied. With this expanded level of detail, vendors can make more informed decisions and devise effective strategies to gain a competitive edge in the market.

Recent Developments
  • Signal: UK Clinical Research Provider Ergomed Bought Out in USD 888 Million Deal

    Permira, a UK private equity firm, agreed to acquire Ergomed for USD 888.1 million. Ergomed is a clinical trial development and management services provider, catering to clients across more than 100 countries. This strategic acquisition can expand Permira's already impressive portfolio of medical companies, including Neurapharm and Cambrex. [Published On: 2023-09-04]

  • Thermo Fisher Scientific Launches New Smart Refrigerator Series

    Thermo Fisher Scientific introduced the Thermo Scientific TM TSG series refrigerators, specifically engineered to cater to the stringent demands of diverse industries. These cutting-edge refrigerators leverage advanced technology to ensure accurate temperature control, effectively preserving the integrity of vaccines and pharmaceuticals. By minimizing temperature fluctuations, these refrigerators effectively mitigate the risks associated with such variations, safeguarding medical products' potency and efficacy. [Published On: 2023-08-16]

  • Loftware and Tenthpin Collaborate on Clinical Supply Labeling

    Loftware and Tenthpin collaborated to launch a software called Loftware Prisym 360, which is specifically designed for clinical supply labeling. The main objective of this partnership is to address the growing challenges faced by clinical trial supply teams within the pharmaceutical industry. This agreement enables both Loftware and Tenthpin to actively promote, educate, and implement a comprehensive content and labeling solution for their clinical customers. [Published On: 2023-08-02]

Key Company Profiles

The report delves into recent significant developments in the Clinical Trial Supplies Market, highlighting leading vendors and their innovative profiles. These include 3M Company, Abbott Laboratories, Almac Group Limited, B. Braun SE, Baxter International, Inc., Bayer AG, Becton, Dickinson and Company, Bio-Rad Laboratories, Inc., Bruker Corporation, Cardinal Health, Inc., Charles River Laboratories, Inc., COREX LOGISTICS LIMITED, Emsere B.V by Medicapital Holdco B.V., Eppendorf SE, Evident Corporation by Olympus Corporation, F. Hoffmann-La Roche Ltd., Fujifilm Group, Hipro Biotechnology Co., Ltd., Hitachi, Ltd., HORIBA, Ltd., ICON PLC, Immudex ApS, Incyte Corporation, IQVIA Inc., Johnson & Johnson Services, Inc., KLIFO A/S, Labnet International, Leica Microsystems GmbH by Danaher Corporation, llumina, Inc., Lonza Group Ltd., Medline Industries, LP, Merck KGaA, Myonex, LLC, Novo Nordisk A/S, Nuvisan GmbH, Parexel International Corporation, Perceptive Informatics LLC and its affiliates, d/b/a Calyx, PerkinElmer Inc. by Revvity, Inc., Pfizer Inc., Promega Corporation, Recipharm AB, Rubicon Research Pvt. Ltd., Sekisui Diagnostics Group, Sharp Services, LLC, Siemens Healthcare GmbH, Smith & Nephew PLC, Stryker Corporation, Thermo Fisher Scientific Inc., and Woodley Equipment Company Ltd..

Market Segmentation & Coverage

This research report categorizes the Clinical Trial Supplies Market to forecast the revenues and analyze trends in each of the following sub-markets:

  • Phase
    • Phase I
    • Phase II
    • Phase III
    • Phase IV
  • Туре
    • Biologic Drugs
    • Medical Devices
    • Small-Molecules
  • Product
    • Auxiliary Medicinal Products
    • Interactive Response Technology (IRT) solutions
    • Lab Supplies
      • Centrifuges
      • Microscopes
      • Pipettes
      • Reagents
    • Medical Devices & Diagnostics
    • Pharmacy Supplies
      • Biohazard Bags
      • Compounding Aseptic Isolators
      • Sterilization Equipment
    • Research Materials
    • Safety Equipment
  • Therapeutic Area
    • Cardiology
    • Genetic Diseases
    • Immunology
    • Infectious Diseases
    • Metabolic Disorders
    • Neurology
    • Oncology
  • End User
    • Contract Research Organisations
    • Pharmaceutical & Biotechnology Companies

  • Region
    • Americas
      • Argentina
      • Brazil
      • Canada
      • Mexico
      • United States
        • California
        • Florida
        • Illinois
        • New York
        • Ohio
        • Pennsylvania
        • Texas
    • Asia-Pacific
      • Australia
      • China
      • India
      • Indonesia
      • Japan
      • Malaysia
      • Philippines
      • Singapore
      • South Korea
      • Taiwan
      • Thailand
      • Vietnam
    • Europe, Middle East & Africa
      • Denmark
      • Egypt
      • Finland
      • France
      • Germany
      • Israel
      • Italy
      • Netherlands
      • Nigeria
      • Norway
      • Poland
      • Qatar
      • Russia
      • Saudi Arabia
      • South Africa
      • Spain
      • Sweden
      • Switzerland
      • Turkey
      • United Arab Emirates
      • United Kingdom

The report offers valuable insights on the following aspects:

  1. Market Penetration: It presents comprehensive information on the market provided by key players.
  2. Market Development: It delves deep into lucrative emerging markets and analyzes the penetration across mature market segments.
  3. Market Diversification: It provides detailed information on new product launches, untapped geographic regions, recent developments, and investments.
  4. Competitive Assessment & Intelligence: It conducts an exhaustive assessment of market shares, strategies, products, certifications, regulatory approvals, patent landscape, and manufacturing capabilities of the leading players.
  5. Product Development & Innovation: It offers intelligent insights on future technologies, R&D activities, and breakthrough product developments.

The report addresses key questions such as:

  1. What is the market size and forecast of the Clinical Trial Supplies Market?
  2. Which products, segments, applications, and areas should one consider investing in over the forecast period in the Clinical Trial Supplies Market?
  3. What are the technology trends and regulatory frameworks in the Clinical Trial Supplies Market?
  4. What is the market share of the leading vendors in the Clinical Trial Supplies Market?
  5. Which modes and strategic moves are suitable for entering the Clinical Trial Supplies Market?

Table of Contents
  1. Preface
  2. Research Methodology
  3. Executive Summary
  4. Market Overview
  5. Market Insights
  6. Clinical Trial Supplies Market, by Phase
  7. Clinical Trial Supplies Market, by Туре
  8. Clinical Trial Supplies Market, by Product
  9. Clinical Trial Supplies Market, by Therapeutic Area
  10. Clinical Trial Supplies Market, by End User
  11. Americas Clinical Trial Supplies Market
  12. Asia-Pacific Clinical Trial Supplies Market
  13. Europe, Middle East & Africa Clinical Trial Supplies Market
  14. Competitive Landscape
  15. Competitive Portfolio
  16. List of Figures [Total: 26]
  17. List of Tables [Total: 664]
  18. List of Companies Mentioned [Total: 49]
In the Lab and Beyond: The Journey of Clinical Trial Supplies
February 12, 2024
INSIGHT
In the Lab and Beyond: The Journey of Clinical Trial Supplies
In the quest for medical breakthroughs, clinical trial supplies construct the ground. These silent orchestrators ensure precision in advancing healthcare by guiding regulations, prioritizing patients, and embracing technology.

Clinical trials are the bedrock of medical improvement, encouraging the evaluation of new drugs, devices, and interventions. At the soul of this process is a meticulous technique for managing clinical trial supplies, containing everything from investigational products to the tools used for data collection.

The landscape of clinical trial supplies is overseen by stringent regulatory requirements to secure the integrity and reliability of trial outcomes. From Good Clinical Practice (GCP) guidelines to regulations set forth by health authorities, compliance is non-negotiable.

Precise forecasting of clinical trial supplies is a craft. Unanticipated changes in trial timelines or patient registration rates can disrupt carefully laid plans. Relentless planning and contingency measures are essential to adapt to the unpredictable nature of clinical trials. In March 2023, Calyx launched the Supply Simulation Service for forecasting and optimizing clinical trial supplies to foresee how long an existing amount of study medication lasts.

The integration of technology has revolutionized the management of clinical trial supplies. Electronic Clinical Trial Management Systems (eCTMS) and Interactive Response Technology (IRT) platforms simplify processes, delivering real-time visibility into inventory levels, site requirements, and participant data.

As the curtain falls on the intricate world of clinical trial supplies, it becomes prominent that these logistical intricacies are the unsung heroes of medical progress. The meticulous planning, adherence to regulations, and technological integration collectively contribute to the successful execution of clinical trials.

Frequently Asked Questions
  1. How big is the Clinical Trial Supplies Market?
    Ans. The Global Clinical Trial Supplies Market size was estimated at USD 3.35 billion in 2023 and expected to reach USD 3.64 billion in 2024.
  2. What is the Clinical Trial Supplies Market growth?
    Ans. The Global Clinical Trial Supplies Market to grow USD 5.92 billion by 2030, at a CAGR of 8.43%
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