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Simulations Plus Supports New FDA Roadmap for Reducing Animal Testing in Preclinical Safety Studies

1. Simulations Plus supports FDA's roadmap to reduce animal testing with NAMs. 2. This aligns with SLP's market offerings in biosimulation and cheminformatics.

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FAQ

Why Bullish?

SLP's support for FDA initiatives highlights its commitment to innovation. Historical examples show that companies aligned with regulatory trends often see positive market reception.

How important is it?

The article addresses regulatory support directly related to SLP's core business, enhancing its market appeal.

Why Long Term?

As regulatory frameworks evolve towards NAMs, SLP is positioned for sustained growth. Companies adopting innovative practices typically benefit over extended periods.

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RESEARCH TRIANGLE PARK, N.C.--(BUSINESS WIRE)--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 announced its support of the U.S. Food and Drug Administration's (FDA) recently announced roadmap for reducing animal testing through the use of new approach methodologies (NAMs). Simulations Plus has long provided the i.

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