This report aims to provide detailed insights
into the global biosimulation
market. It provides valuable information on the
type, procedure, application, and region in the market. Furthermore, the
information for these segments, by region, is also presented in this report.
Leading players in the market are profiled to study their product offerings and
understand the strategies undertaken by them to be competitive in this market.
Expected
Revenue Growth:
The biosimulation market is expected to reach USD 2.88 Billion by 2022
from USD 1.38 Billion in 2017, at a CAGR of 15.9%.
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Key Factors Driving Market Growth:
The
growth of this market is majorly driven by factors such as the increase in
R&D investments in the pharmaceutical and biotechnology industries, growing
adoption of biosimulation software by regulatory bodies, technologically
advanced QSP systems, need to curtail drug discovery and development costs, and
growth in the biologics and biosimilars markets.
Biosimulation software expected to dominate the market in 2017.
Based on product and service, the Biosimulation Market is segmented into
software and services. In 2017, the biosimulation software segment is expected
to account for the largest share of the biological simulation market. The high
growth of this segment is attributed to the growing adoption of biosimulation
software by pharmaceutical and research organizations and the increasing
R&D investment for pharmaceutical research.
Emerging Applications of Biosimulation Industry:
The emerging applications of biosimulation in defense, industrial
bioprocessing, nutraceuticals, and agri-food production present significant
opportunities for the growth of the global biological simulation market.
Various biosimulation companies are adopting inorganic and organic growth
strategies to expand the applications of
their biosimulation software and services. In May 2017, the Institute of Life
Science at Swansea University delivered an in silico drug discovery software
platform for the UK Ministry of Defense for the development of antimicrobials
to meet the needs of defense and security in the country. Likewise, in April
2017, Certara formed a partnership with the Australian Department of Defense.
Certara’s d3 medicine company was selected to conduct a national audit to check
the research and development capabilities and capacity of Australia’s medical
countermeasures (MCM) product.
North America to
dominate the biosimulation market
In 2017, North America is
expected to dominate the biological simulation market followed by Europe. The large
share of this geographical segment is attributed to factors such as growth in
the biotechnology and pharmaceutical industry, a large number of ongoing drug
development processes, increased use of personalized medicine, and increasing
R&D expenditure by pharmaceutical and biotechnology companies.
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Key Market Players:
The Biosimulation Market is highly
competitive with the presence of several small and big players. Some of the
players in the Biosimulation Market include Certara (US), Simulation Plus (US),
Dassault Systèmes (France),
Schrödinger (US), ACD/Labs (Canada),
Chemical Computing Group (Canada),
Physiomics (UK), Evidera (US), In silico biosciences (US), INOSIM Software (Germany), Insilico
Biotechnology (Germany),
LeadInvent Technologies (India),
Rosa (US), Nuventra Pharma (US), and Genedata (Switzerland).
Growth in the global biological
simulation market is mainly driven by factors such as the growing pressure to
curtail healthcare expenditures, growing demand for biosimilars due to their
cost-effectiveness, rising incidence of various diseases, increasing number of
off-patented drugs, positive outcomes in ongoing clinical trials, and rising
demand for biosimilars in different therapeutic applications such as rheumatoid
arthritis and blood disorders. As there is very little success in the R&D
of new chemical entities, pharmaceutical companies are trying to find new
applications for their existing drugs. As toxicity and other vital parameters
of drug safety are already tested, biosimulation technologies are used to
confirm the hypothesis of using the drugs for a new indication or disease.