PUBLISHER: Fairfield Market Research | PRODUCT CODE: 1394159
PUBLISHER: Fairfield Market Research | PRODUCT CODE: 1394159
A recent market analysis report by Fairfield Market Research reveals that the global Preclinical Contract Research Organization (CRO) market achieved sales of US$ 5.9 billion in 2024. The market is poised to attain a valuation of US$ 12 billion by 2031. Toxicology Testing is anticipated to be the leading revenue-generating segment during forecast period 2024 to 2031.
Regulatory Constraints: Stringent regulatory norms for preclinical CRO services, including Good Laboratory Practice (GLP) regulations established by organizations like the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA), can pose challenges to the industry. Compliance with quality control standards is essential but may restrict market expansion, as certain advanced tests like genotoxicity are often conducted in-house by pharmaceutical companies due to regulatory requirements.
Rise of Biopharmaceutical Companies: The surge in biopharmaceutical companies worldwide, especially in developing and emerging countries, has led to an increased demand for preclinical CRO services. Smaller biopharmaceutical companies, lacking the resources and expertise for in-house preclinical research, are outsourcing these activities to preclinical CROs. The growing number of biopharmaceutical companies is a significant driver of the global preclinical CRO market.
Increased Disease Burden: The rising prevalence of diseases has prompted a growing demand for clinical tools and diagnostic equipment that can provide quick and reliable results while being safe. This trend has further boosted the demand for preclinical CRO services, particularly from medical device companies, contributing to the growth of the market.
North America: North America presents substantial opportunities in the preclinical CRO market. Increased research and development investments, along with rapid adoption of new technologies, are expected to drive significant market growth in the region. The availability of skilled workforce and affordable equipment costs are additional factors fueling market expansion. The region is also witnessing a rising burden of chronic diseases, further driving demand for preclinical CRO services.
Asia Pacific: The Asia Pacific region is poised for rapid growth due to the cost-effectiveness of preclinical CRO services in countries like India and China. The establishment of numerous contract research organizations (CROs) in the region has strengthened the preclinical outsourcing industry. For instance, Singapore hosts several contract research organizations that cater to the growing needs of pharmaceutical and biopharmaceutical companies.
Toxicology Testing: The Toxicology Testing segment is projected to grow at a CAGR of 10% during the forecast period. The rise in outsourcing of noncore preclinical CRO studies and increased adoption of toxicology tests are driving this growth. The dynamic growth in the biopharmaceutical and pharmaceutical sectors, coupled with the demand for new drugs and chemicals, is expected to further propel the market. Toxicology Testing plays a vital role in Investigational New Drug (IND)-enabling studies, contributing significantly to the segment's growth.
The rapid adoption of advanced healthcare technologies to enhance healthcare delivery is a key factor driving competitiveness in the market. Leading firms are pursuing mergers, acquisitions, and new product launches to maintain market share and diversify their product portfolios. In response to the ongoing COVID-19 pandemic, major market participants are offering various services to address the challenging conditions.