Global clinical trial supplies market is projected to witness a CAGR of 7.97% during the forecast period 2024–2031, growing from USD 3.01 billion in 2023 to USD 5.56 billion in 2031. The market has experienced significant growth in recent years and is expected to maintain a strong pace of expansion in the coming years.
Clinical trial is an essential step in developing any drug through which the developers ensure the safety and efficacy of any drug. This step is mandatory for any drug or chemical product before its launch to ensure public safety. The market is growing manifold due to factors such as advancing technology, increasing population and cases of chronic diseases, increasing need for clinical trials, increasing demand for drugs and chemical products and the rising regulatory requirements to ensure patient safety. Additionally, the industry has seen the launch of smart devices that provide precise and quick findings that are helpful in research and development. Companies and practitioners are collaborating to provide the best technology for industry professionals. Both public and commercial organizations are raising money and investing a sizable sum of it to be able to provide quality solutions. These massive corporations use strategic maneuvers like collaborations, investments, and mergers and acquisitions when they are striving to develop or introduce a new product. For instance, a strategic partnership between ICON plc (Ireland) and LEO Pharma (Denmark) was formed in March 2023 to improve LEO Pharma’s clinical trial operations, emphasizing cost-effectiveness and patient-centricity.
Thermo Fisher Scientific Inc. (US) and the National Minority Quality Forum (NMQF), an independent non-profit organization devoted to research and education, partnered in September 2023. The goal of this partnership, which is made possible by NMQF’s Alliance for Representative Clinical Trials (ARC), is to increase the participation of patient groups who have historically been underrepresented in clinical research.
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Growing Need for Clinical Trials Fuels Market Growth
Clinical trials are essential for expanding our understanding of medicine, assessing novel cures, and enhancing patient care. The expanding number of registered trials reflects the increased interest in medical research, the creation of novel treatments, and the understanding of the significance of evidence-based medicine. According to the United States National Library of Medicine, there are 452,604 studies registered on Clinicaltrials.gov, with locations in all 50 states and 221 countries worldwide. The quick development of medical research and technology is one of the main causes of the rise in registered clinical trials. New research directions have been made possible by identifying novel disease targets, advancements in the knowledge of molecular mechanisms, and developments in fields such as immunology, regenerative medicine, and genomics. As a result, there has been a significant increase in the creation of innovative treatments and interventions, increasing the demand for clinical studies to assess their efficacy and safety.
Furthermore, the public, researchers, and healthcare professionals are becoming more aware of the value of evidence-based medicine.
A methodical and thorough way to assess the effectiveness and safety of medical therapies is through clinical trials. More academics and organizations are conducting clinical trials in response to the growing need for evidence-based medicine to produce high-quality data that can inform medical decisions and enhance patient outcomes. Moreover, the rise of registered trials can also be attributed to the globalization of clinical research. Clinical trials used to be mostly carried out in industrialized nations. Nonetheless, there has been a notable change in the direction of conducting trials in other geographical areas, such as developing and emerging markets. As of May 17, 2023, clinicaltrials.gov reports 140,268 registered studies overall. However, there have been about 240,844 registered studies in countries apart from the United States. Numerous variables are driving this increase, including easier access to larger patient populations, a wider range of genetic origins, lower prices, and quicker regulatory pathways. Consequently, many clinical trials have been filed in areas previously underrepresented in medical research, driving market growth.
Rising Regulatory Requirements to Ensure Patient Safety
The market for clinical trials is expanding due to the need for safety evaluations of novel drugs and compounds. Strict regulatory requirements requiring thorough toxicity studies serve as the driving force for these assessments. Modern technological developments like organ-on-a-chip models and high-throughput screening have eliminated the practice of animal research. It has been demonstrated that these novel models improve the accuracy and relevance of the predictions in the tests. Furthermore, because of the increased safety concerns surrounding high-profile medication withdrawals, thorough safety assessments have become increasingly necessary throughout the drug development process. In addition to saving money and time, in-vitro testing contributes to the healthy expansion of the biotechnology and pharmaceutical industries by enabling the creation of safer and more effective therapeutic agents to meet the growing incidence of chronic diseases and aging populations.
For example, Parexel International Corp, a global clinical research organization (CRO) that focuses on the discovery and delivery of innovative new therapies to enhance patient health, announced the development of a new clinical trial supply and logistics depot in Suzhou, China, in September 2022. This well-placed facility provides quick access to supplies and investigational therapeutics for delivery to clinical locations and patients worldwide for domestic and foreign biopharmaceutical companies conducting clinical studies.
Thermo Fisher Scientific Inc. stated in October 2022 that it will increase operations in Kentucky to assist clients by providing patients with life-altering medications. The current facility offers biomarker and central lab services, giving biopharma customers access to top-notch lab work to expedite the drug development. Additionally, this has increased the company’s global visibility and allowed it to grow its diagnostics business throughout the globe.
Growth in Demand for Biologics to Fuel Market Growth
Biologics and biosimilars are manufactured using extremely intricate procedures from living cells, and their market share is predicted to increase steadily because of growing research into biotechnology and genetics, including the development of biosimilar products and nanoparticle-based drug delivery systems. Biologics, which include hormones, blood products, vaccines, genes, insulin, and monoclonal antibody (mAb) products, are being used as the most cutting-edge treatments for autoimmune illnesses such as rheumatoid arthritis and Crohn’s disease. Over the projected time, biologics have grown significantly due to their growing demand and clinical benefits. For instance, five biosimilars were approved by the Center for Drug Evaluation and Research (CDER) in 2023, three of which were biosimilars for reference products for which there was no prior biosimilar. For 14 reference products, CDER has authorized 45 biosimilars so far. Several products were authorized as interchangeable biosimilars, which can be interchanged for the reference product at a pharmacy, like generics that are substituted subject to state law. CDER has approved seven interchangeable biosimilars.
The number of cancer cases is rising quickly, and researchers are becoming more innovative in their approaches to using biologics for treating cancer. In an article published in January 2022 by the American Cancer Society Journal, the number of cancer cases reported has gone up to approximately 1.9 million in the United States in 2022. Biologics therapy is becoming more popular than standard cancer treatment because it uses the body’s natural immune systems and healing capabilities to either combat cancer or repair healthy tissue following treatment. Therefore, more cancer cases fuel biologics expansion, so the biologics segment is predicted to expand significantly.
The global clinical trial supplies market is an essential component of the pharmaceutical and biotechnology industries, ensuring that clinical trials run smoothly and effectively. With the increasing number of clinical trials worldwide, the demand for reliable and efficient clinical trial supplies is rising. This blog post explores the growth of the global clinical trial supplies market, highlighting key trends, challenges, and future prospects.
Understanding Clinical Trial Supplies
Clinical trial supplies refer to the materials and logistics required to conduct clinical trials. This includes investigational drugs, placebos, comparator drugs, laboratory supplies, and various support services such as packaging, labeling, storage, and distribution. The successful execution of clinical trials depends heavily on the timely and efficient supply of these materials.
Market Size and Growth
The global clinical trial supplies market is currently valued at around $2.5 billion and is projected to grow at a compound annual growth rate (CAGR) of approximately 7–8% over the next five years. Several factors are driving this growth:
- Increase in Clinical Trials: The surge in the number of clinical trials, especially in emerging markets, is a significant growth driver.
- Complexity of Trials: Modern clinical trials are becoming increasingly complex, requiring sophisticated supply chain solutions.
- Focus on Personalized Medicine: The rise of personalized medicine and biologics is creating a demand for specialized clinical trial supplies.
- Regulatory Requirements: Stringent regulatory requirements necessitate high-quality and compliant supplies, driving market growth.
Key Trends Shaping the Market
- Adoption of Advanced Technologies: The use of advanced technologies such as blockchain, artificial intelligence (AI), and machine learning (ML) is transforming the clinical trial supplies market. These technologies enhance supply chain transparency, optimize inventory management, and improve data accuracy.
- Decentralized Clinical Trials (DCTs): The trend towards decentralized clinical trials, accelerated by the COVID-19 pandemic, is reshaping the market. DCTs require innovative supply solutions to manage the distribution of supplies to diverse and remote locations.
- Sustainability: Environmental sustainability is becoming a priority, with companies focusing on eco-friendly packaging and supply chain practices.
- Outsourcing: The outsourcing of clinical trial supply management to specialized service providers is on the rise, enabling pharmaceutical companies to focus on their core competencies.
North America to Dominate the Clinical Trial Supplies Market
The increasing number of clinical trials is why North America has the largest global market for clinical trial supplies. The North American clinical trial supply industry is driven by rising government funding, increasing disease prevalence, and a growing number of clinical trials. Since more large-scale pharmaceutical R&D clinical trials are carried out in this region, many CROs and biopharmaceutical businesses have established their headquarters in the United States and Canada. The most efficient regulation of clinical trials with advanced therapy, including electronic records and signatures, protection of human subjects, and good clinical practices for non-clinical laboratory studies, eases the process of conducting clinical trials overall. Significant R&D investments are being made due to high cancer prevalence in the United States, another factor propelling North America’s clinical trial supply market.
According to the cancer facts and figures report for 2023 from the American Cancer Society, approximately 1.9 million new cancer cases were diagnosed in 2023. Notably, prostate cancer is projected to lead with an estimated 288,300 cases, followed by lung cancer with 238,340 cases, and female breast cancer with 300,590 cases. Similarly, data released by the Government of Canada in May 2022 revealed that around 233,900 Canadians received cancer diagnoses in 2022, with prostate cancer anticipated to remain the most commonly diagnosed type of cancer. The market for clinical trial supplies in North America is therefore being driven by the rising number of cancer cases that are recorded each year. Therefore, for the reasons outlined above, the North American clinical trial supplies market is the largest and is anticipated to develop significantly throughout the projected period. In August 2022, Marken Ltd. (US) purchased Bomi Group to support the expansion of healthcare logistics by expanding the company’s international presence and strengthening cold chain capabilities in important European and Latin American markets.
Future Market Scenario (2024–2031F)
One of the main factors contributing to the anticipated growth of the clinical trial supplies market is the increasing demand for clinical trial services to ensure patient safety by delivering the right quality of drugs. The rising population and increasing cases of chronic diseases such as cardiovascular diseases, diabetes, and cancer will also propel the market growth in the forecast period. Players in this market are expanding at an unparalleled rate, introducing cost-effective and efficient technologies. For instance, the IXRS 3 Partnership Network was unveiled by Almac Group Limited (UK) in April 2023 to accelerate developing and implementing cutting-edge eClinical solutions for biopharmaceutical sponsors.
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