Simulations Plus Supported Development of Majority of FDA-Approved Drugs in 2024
14 Januar 2025 - 1:13AM
Business Wire
SLP’s technology and expertise accelerates
drug development and supports critical advancements in global
healthcare
Simulations Plus, Inc. (Nasdaq: SLP) (“Simulations Plus”), a
leading provider of cheminformatics, biosimulation,
simulation-enabled performance and intelligence solutions, and
medical communications to the biopharma industry, today highlighted
its impact on the pharmaceutical industry through supporting the
development of a majority of the drugs approved by the U.S. Food
and Drug Administration (FDA) in 2024.
“For more than 25 years, our clients have entrusted us to
provide the mission-critical software and services needed to
develop therapies that are changing the landscape of healthcare,”
said Shawn O’Connor, Chief Executive Officer at Simulations Plus.
“We are proud that our advanced modeling and simulation software
and consulting services supported the development of the majority
of drugs approved by the FDA in 2024. This achievement underscores
the increasing role that innovative technologies and collaborative
expertise plays in accelerating the drug development process. As
global health challenges grow, we remain committed to delivering
solutions which help advance life-saving therapies that improve
patient outcomes worldwide.”
Simulations Plus offers software and consulting services that
enhance drug discovery, development, research, clinical trial
operations, regulatory submissions, and commercialization. SLP’s
suite of solutions leverage artificial intelligence/machine
learning (AI/ML), physiologically based
pharmacokinetics/physiologically based biopharmaceutics
(PBPK/PBBM), quantitative systems pharmacology/quantitative systems
toxicology (QSP/QST), and population PK/PD modeling approaches, as
well as adaptive learning and medical communications tools.
About Simulations Plus, Inc.
With more than 25 years of experience serving clients globally,
Simulations Plus stands as a premier provider in the biopharma
sector, offering advanced software and consulting services that
enhance drug discovery, development, research, clinical trial
operations, regulatory submissions, and commercialization. Our
comprehensive biosimulation solutions integrate artificial
intelligence/machine learning (AI/ML), physiologically based
pharmacokinetics, physiologically based biopharmaceutics,
quantitative systems pharmacology/toxicology, and population PK/PD
modeling approaches. We also deliver simulation-enabled performance
and intelligence solutions alongside medical communications support
for clinical and commercial drug development. Our cutting-edge
technology is licensed and utilized by leading pharmaceutical,
biotechnology, and regulatory agencies worldwide. For more
information, visit our website at www.simulations-plus.com. Follow
us on LinkedIn | X | YouTube.
Environmental, Social, and Governance (ESG)
We focus our Environmental, Social, and Governance (ESG) efforts
where we can have the most positive impact. To learn more about our
latest initiatives and priorities, please visit our website to read
our 2023 ESG update.
Forward-Looking Statements
Except for historical information, the matters discussed in this
press release are forward-looking statements that involve risks and
uncertainties. Words like “believe,” “expect,” and “anticipate”
mean that these are our best estimates as of this writing, but
there can be no assurances that expected or anticipated results or
events will actually take place, so our actual future results could
differ significantly from those statements. Factors that could
cause or contribute to such differences include, but are not
limited to: our ability to successfully integrate the Pro-ficiency
business with our own, as well as expenses we may incur in
connection therewith, the efficiency and effectiveness of our
internal business restructuring and leadership changes, our ability
to maintain our competitive advantages, acceptance of new software
and improved versions of our existing software by our customers,
the general economics of the pharmaceutical industry, our ability
to finance growth, our ability to continue to attract and retain
highly qualified technical staff, market conditions, macroeconomic
factors, and a sustainable market. Further information on our risk
factors is contained in our quarterly and annual reports and filed
with the U.S. Securities and Exchange Commission.
View source
version on businesswire.com: https://www.businesswire.com/news/home/20250113170308/en/
Financial Profiles Lisa Fortuna
310-622-8251 slp@finprofiles.com
Simulations Plus (NASDAQ:SLP)
Historical Stock Chart
Von Dez 2024 bis Jan 2025
Simulations Plus (NASDAQ:SLP)
Historical Stock Chart
Von Jan 2024 bis Jan 2025