The global virtual clinical trials market size was estimated at USD 7.0 billion in 2019 and is expected to expand at a compound annual growth rate (CAGR) of 5.1% from 2020 to 2027. The market is majorly driven by a rise in R&D activities, the increasing healthcare digitization, as well as the adoption of telehealth. Besides, technological advancements, alliances between clinical research organizations, pharmaceutical, and biotechnology companies, as well as supportive government initiatives are anticipated to drive the market.
A virtual trial follows a patient-centered approach, allowing for a more conventional trial experience for the participant together with enhanced data collection, increased diversity of patient, and time savings from the perspective of the trial duration. It takes complete advantage of many digital tools available and is characterized by no physical visits to a trial site. There is no shortage of terms or labels being utilized to define the concept of virtual trials. From virtual to mobile-enabled, to direct-to-patient, to remote, to software-enabled, to site-less, to modern, to 21st-century clinical trials, to flexible, to digitally-enabled, the list goes on.
The current COVID-19 pandemic is forcing the clinical trial industry to change the way of conducting ongoing or upcoming trials. This year has changed people’s lives upside down. The stay-at-home and quarantine orders are being followed everywhere and the clinical trial industry is no exception. As per the Continuum Clinical report published in April 2020, approximately 30% of the surveyed clinical trial places are projected to have seen a huge impact on recruiting patients for new trial studies as well as retaining already-enrolled patients compliant with their study schedules. Also, 81% of the European clinical trial study sites and 56% of the U.S. sites indicated that the patients are less likely to continue participating in studies. Besides, as of March 30, around 30 pharma or biotech companies have reported disruption to a trial as a result of the crisis.
Virtual trials, also known as decentralized trials, have a significant role to play in the present COVID-19 crisis and are set to become a norm in the way trials and real-world studies are run. A virtual method allows people to take part in the trial from their homes ensuring that research can be continued even when site visits are not possible. In addition, it is a novel approach to collecting safe and effective data from participants of clinical studies.
Virtual visits and remote patient monitoring of in-person site visits give participants a choice and peace of mind of not exposing to unnecessary risks. The virtual studies enable sponsors to include a larger population in the study, thus improving recruitment, engagement, and retention. Also, it enables continuous real-time data collection through digital health technologies. Eventually, virtual connectivity, monitoring as well as management can significantly decrease the effort, time commitment, and burden on the participants, CRCs, and investigators.
The oncology segment dominated the market and accounted for the largest revenue share of 25.0% in 2019. The segment is also anticipated to contribute to the maximum revenue share of the market during the forecast period. This is attributed to the rising cases of cancer globally and the increasing number of oncology clinical trials. Cancer patients are the most vulnerable during the COVID-19 pandemic. Investigators and sponsors managing oncology clinical trials have quickly incorporated virtual and remote trials to keep patients safe and keep the trials moving forward.
Besides, cancer researchers face considerable challenges in patient recruitment. As of June 2019, approximately 14,000 oncology trials were actively recruiting with a participation rate of 3.0% to 8.0% of possible candidates, with a limited number in minority and geriatric populations. A low rate of enrollment poses risks to the success of specific clinical studies. It may hamper the treatment advances and corresponding benefits to outcomes. Hence, the low recruitment rate and the need for a diverse population for oncology clinical studies are anticipated to boost the adoption of virtual clinical trials.
The interventional segment dominated the market and accounted for the largest revenue share of 46.5% in 2019. The rapid increase in the number of experiments to develop novel medications for various diseases, and the digitalization of laboratories are driving the segment growth. The outbreak of coronavirus has raised the demand for testing and trials of new drugs and vaccines to combat the situation around the world, as traditional methods of clinical trials come with a huge risk of infection in people.
The virtual trials are better suited for chronic diseases as well as less interventional observational studies including cardiovascular diseases, immunology, gastrointestinal, dermatology, respiratory, and endocrinology. The firm that first started this concept conducted an entire interventional Phase2b “site-less” clinical trial with 372 patients across 10 states using their proprietary mobile telemedicine-based platform named “NORA”.
North America accounted for the largest revenue share of 49.7% of the virtual clinical trials market in 2019. The region is expected to continue its dominance over the forecast period. This can be attributed to increasing R&D in this region, the increasing adoption of new technologies in clinical research, as well as government support. Furthermore, market players are also using digital technologies to meet client needs. For instance, Parexel performed more than 100 virtual clinical trials including hybrid and virtual approaches. Covance also has around 1,900 LabCorp Patient Service Centers across the U.S. that brings the trial to patients.
In Asia Pacific, the market is anticipated to witness the fastest CAGR of 6.2% during the forecast period owing to the increasing availability of a large patient pool enabling easy recruitment of candidates, & enhanced penetration of digital technologies in the region. Furthermore, the outbreak of coronavirus is anticipated to boost the adoption of telemedicine, thereby driving the market in the region.
The market for virtual clinical trials is highly competitive in nature. A significant factor affecting the competitive nature of the market is the quick adoption of advanced technology for improved healthcare. Besides, players are also acquiring, collaborating, and partnering with other firms to gain market share. For instance, in May 2020, Covance announced the expansion of its technology ecosystem to accelerate the adoption of virtual clinical trials. The company is doing so through an alliance with Medable, a prominent software provider for digital clinical trials. Some of the prominent players in the virtual clinical trials market include:
PRA Health Sciences
Medidata
Medpace
Medable, Inc.
LEO Innovation Lab
Clinical Ink
Report Attribute |
Details |
Market Size value in 2020 |
USD 7.4 billion |
Revenue forecast in 2027 |
USD 10.5 billion |
Growth Rate |
CAGR of 5.1% from 2020 to 2027 |
Base year for estimation |
2019 |
Historical data |
2016 - 2018 |
Forecast period |
2020 - 2027 |
Quantitative units |
Revenue in USD million and CAGR from 2020 to 2027 |
Report coverage |
Revenue forecast, company ranking, competitive landscape, growth factors, and trends |
Segments covered |
Study design, indication, region |
Regional scope |
North America; Europe; Asia Pacific; Latin America; Middle East & Africa |
Country scope |
U.S.; Canada; U.K.; Germany; France; Italy; Spain; India; Japan; China; Australia; South Korea; Brazil; Mexico; Argentina; Colombia; South Africa; Saudi Arabia; UAE |
Report coverage |
Revenue forecast, company share, competitive landscape, growth factors, and trends |
Key companies profiled |
IQVIA; ICON Plc; Covance; PAREXEL International Corporation; PRA Health Sciences; Medidata; Medpace; Medable, Inc.; LEO Innovation Lab; Clinical Ink |
Customization scope |
Free report customization (equivalent up to 8 analyst’s working days) with purchase. Addition or alteration to country, regional & segment scope. |
Pricing and purchase options |
Avail customized purchase options to meet your exact research needs. Explore purchase options |
This report forecasts revenue growth at global, regional, and country levels and provides an analysis of the latest industry trends in each of the sub-segments from 2016 to 2027. For the purpose of this study, Grand View Research has segmented the global virtual clinical trials market report on the basis of study design, indication, and region:
Study Design Outlook (Revenue, USD Million, 2016 - 2027)
Interventional
Observational
Expanded Access
Indication Outlook (Revenue, USD Million, 2016 - 2027)
Oncology
Cardiovascular
Others
Regional Outlook (Revenue, USD Million, 2016 - 2027)
North America
U.S.
Canada
Europe
U.K.
Germany
France
Italy
Spain
Asia Pacific
India
Japan
China
Australia
South Korea
Latin America
Brazil
Mexico
Argentina
Colombia
Middle East & Africa
South Africa
Saudi Arabia
UAE
b. The global virtual clinical trials market size was estimated at USD 7.0 billion in 2019 and is expected to reach USD 7.4 billion in 2020.
b. The global virtual clinical trials market is expected to grow at a compound annual growth rate of 5.1% from 2020 to 2027 to reach USD 10.5 billion by 2027.
b. North America dominated the virtual clinical trials market with a share of 49.7% in 2019. This is attributable to rising healthcare awareness coupled with rising healthcare expenditure, high disposable income, and constant research and development initiatives.
b. Some key players operating in the virtual clinical trials market include Iconplc, LEO Innovation Lab, Science 37, IQVIA, PRA Health Sciences, Clinical Ink, Parexel, Medable, and Covance.
b. Key factors driving the virtual clinical trials market growth include increasing prevalence of diseases and high demand for clinical trials, rising demand rising research and development to deliver advanced healthcare infrastructure, increasing per capita income, and favorable government initiatives.
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