The global drug discovery outsourcing market size was estimated at USD 2.19 billion in 2016. Drug discovery is a long, costly, and arduous process that requires dedicated manpower, financial resources, and infrastructure. The pharmaceutical industry has witnessed radical changes in the past two decades, in terms of a shift toward biologics, patent expiration, and unprecedented downsizing of internal discovery of big pharmaceuticals. All of this has accelerated the adoption of outsourcing activities.
Breaking down the different steps of drug discovery such as hit confirmation, lead generation, lead optimization, and high-speed screening allows players to specialize in their core services. An estimated 75.0% to 80.0% of R&D spending in the biopharmaceutical industry can be outsourced, creating opportunities for contract research organizations (CROs). High demand for novel drug candidates drives R&D in the pharmaceutical industry, which in turn, is expected to boost market growth.
Increase in number of potential targets over the past years is much faster than the rise in information related to these targets. This has added to the challenges faced by drug discoverers. It is projected that over the next few years almost one-half of drug discovery practices will be outsourced, thereby accelerating revenue growth.
Innovation and technological advancements have dynamically changed drug discovery research. Combination of chemistry-based and target-based technologies identification of novel compounds demand technical expertise. These include molecular and behavioral pharmacology, ultra-high-throughput screening (ultra-HTS), molecular biology, and medicinal, combinatorial, and analytical chemistry.
Key biopharmaceutical companies have been observed collaborating with academia and CROs for drug discovery. Cost cutting, chasing innovation, gaining access to specialized knowledge and technology, and increasing speed and agility are some of the significant factors encouraging pharma companies to expand their involvement in outsourcing. This, in return, is expected to increase competition among key players.
For instance, AstraZeneca established multiple outsourcing partnerships with Cancer Research UK (CRUK) Cambridge Institute, Medical Research Council Laboratory of Molecular Biology (MRC LMB), University of Texas MD Anderson Cancer Center, and Academic Drug Discovery Consortium (ADDC) in 2013-14. Other prominent partnerships include Bristol-Myers Squibb with Allied Minds, GlaxoSmithKline with the University of Leicester, and Actelion with Enamine.
The iterative process of lead identification, also known as hit-to-lead, is a significant stage in early drug discovery. It has historically proven to have improved efficiencies and economies of scale for drug developers. Introduction of advanced in silico techniques to improve lead identification process, such as Computer-Aided Drug Discovery (CADD) and structure-based drug designs, support segment growth.
Advances in High Throughput Screening (HTS) technology, which enables screening of rare metabolically active tumor cells, microchip-synthesized genes, and toxicology of environmental chemicals and drugs, benefits the growth of the segment.
Need for resources with combinational knowledge of metabolism, analytical chemistry, and computer software, along with high cost associated with integration of latest computation technology, is enabling higher outsourcing of lead identification. As a result, lead identification and candidate optimization accounted for the largest share in terms of revenue in 2016.
The other associated services segment, which includes data mining, is anticipated to witness rapid growth in the coming years. This is owing to increased adoption of outsourcing services and high investments in drug discovery R&D.
Respiratory systems accounted for largest share in the drug discovery outsourcing market in 2016. Higher adoption of drug discovery outsourcing, coupled with well-established product portfolio resulting from outsourcing, is responsible for the segment’s high revenue. High incidence of respiratory disorders such as lung cancer, bronchitis, tuberculosis, chronic obstructive pulmonary diseases (COPD), and asthma, coupled with increasing cases of drug resistance, has also influenced segment growth.
The oncology and anti-infective segments are both projected to witness strong growth over the course of the forecast period. Increased focus on identification of novel targets to support cancer treatment contributes to lucrative growth of the oncology segment.
Antimicrobial resistance is projected to become a global crisis with its high rate of emergence and spread resulting in high economic burden. Companies have increased R&D in anti-infective drugs, having identified the future need. This is poised to benefit segment growth.
Small molecules pharmaceuticals accounted for the highest number of New Drug Application (NDA) approvals in 2014 and contributed a substantial number of new molecular entities. Furthermore, small molecules represent about two-third of drugs in the pipeline. Increased significance and highly effective components add up to the potential of small molecules in pharmaceutical portfolio. Owing to this, small molecules held the largest share in the overall market.
Furthermore, advantages of small molecules over larger ones have increased investments in the field, especially in cancer research. Ongoing studies to investigate and develop novel therapeutics for various indications is expected to further influence segment growth.
North America dominated the market in 2016 owing to higher adoption of technological advancements, presence of well-established research infrastructure, presence of key players, and higher investments in drug discovery R&D. With outsourcing no longer being solely about cost reduction, rising need for efficiency, quality, and innovation are expected to contribute to market growth.
Government initiatives in emerging Asia Pacific (APAC) countries to forge alliances with U.S. pharmaceutical companies are anticipated to foster regional market growth. In addition, regulatory changes as well as emerging and promising startups have been attracting API and drug development outsourcing to countries such as China and India.
For instance, China launched the Market Authorization Holder (MAH) pilot program, following which, investments from venture capital increased in the nation’s biotech and pharmaceutical sector. Initiatives for economic progress and high investments to raise infrastructure to support R&D further contributes to growth in the APAC market.
Some of the major players are Albany Molecular Research Inc.; EVOTEC;Laboratory Corporation of America Holdings; GenScript; Pharmaceutical Product Development, LLC; Charles River;WuXi AppTec; Merck & Co., Inc.; Thermo Fisher Scientific Inc.; Dalton Pharma Services; Oncodesign; Jubilant Biosys; DiscoverX Corporation; and QIAGEN. International partnerships are a key strategy witnessed among players. For instance, CROs in U.K. are increasingly collaborating with players in the Swiss pharmaceutical sector. Events like the UK Trade & Investment (UKTI) further encourage alliances among players.
In addition, in a fragmented industry like pharmaceutical, agility becomes vital in the fast-moving drug discovery sector and this can be provided by quality service offerings along with a broad portfolio of capabilities. Thus, partnerships with Contract Development and Manufacturing Organizations (CDMOs) are preferred over Contract Manufacturing Organizations (CMOs).
Base year for estimation
Actual estimates/Historical data
2013 - 2016
2017 - 2025
Revenue in USD Million & CAGR from 2017 to 2025
North America, Europe, Asia Pacific, Latin America, Middle East & Africa
U.S., Canada, U.K., Germany, Japan, China, Brazil, South Africa
Revenue forecast, company share, competitive landscape, growth factors and trends
15% free customization scope (equivalent to 5 analyst working days)
If you need specific information, which is not currently within the scope of the report, we will provide it to you as a part of customization
This report forecasts revenue growth at global, regional, and country levels and provides an analysis on latest industry trends and opportunities in each of the sub-segments from 2013 to 2025. For the purpose of this report, Grand View Research has segmented the global drug discovery outsourcing market report on the basis of workflow, therapeutic area, drug type, and region:
Workflow Outlook (Revenue, USD Million, 2013 - 2025)
Target Identification & Screening
Target Validation & Functional Informatics
Lead Identification & Candidate Optimization
Other Associated Workflow
Therapeutic Area Outlook (Revenue, USD Million, 2013 - 2025)
Pain and Anesthesia
Central Nervous System
Drug Type Outlook (Revenue, USD Million, 2013 - 2025)
Large Molecules (Biopharmaceuticals)
Regional Outlook (Revenue, USD Million, 2013 - 2025)
Middle East and Africa (MEA)
b. The global drug discovery outsourcing market size was estimated at USD 2.8 billion in 2019 and is expected to reach USD 3.1 billion in 2020.
b. The global drug discovery outsourcing market is expected to grow at a compound annual growth rate of 8.1% from 2017 to 2025 to reach USD 4.4 billion by 2025.
b. North America dominated the drug discovery outsourcing market with a share of 36.2% in 2019. This is attributable to the higher adoption of technological advancements, the presence of well-established research infrastructure, the presence of key players, and higher investments in drug discovery R&D.
b. Some key players operating in the drug discovery outsourcing market include Albany Molecular Research Inc.; EVOTEC; Laboratory Corporation of America Holdings; GenScript; Pharmaceutical Product Development, LLC; Charles River; WuXi AppTec; Merck & Co., Inc.; Thermo Fisher Scientific Inc.; Dalton Pharma Services; Oncodesign; Jubilant Biosys; DiscoverX Corporation; and QIAGEN.
b. Key factors that are driving the market growth include increasing trends of partnerships in drug discovery research; rising incidence rate of metabolic, genetic, and other chronic diseases; technology advancement in drug discovery.
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Multiple therapeutic regimens are being followed across the globe in attempts to come up with a reliable treatment for Covid-19. One line of treatment includes the use of hydroxychloroquine, while a second treatment line focuses to use antiviral drugs used in the disease management of HIV. Both these approaches have surged demand from advanced antivirals and antimalarial drugs. This impacts the drug manufacturers as an off label indication for these drug classes has to be worked upon. At the moment, the WHO has not prescribed any of these approaches, neither they have commented if one is better than the other. The report will account for Covid19 as a key market contributor.