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HSR clearance advances Altaris bid for Simulations Plus toward a second-half close

Healthcare private equity has been moving at a deliberate pace through this stretch of the deal cycle, and the regulatory calendar for software-driven biopharma tools is now moving to match. Altaris, the New York-based investment…

By Ines Ferreira·August 14, 2026·二〇二六年八月十四日·2 min read

Key takeaways

  • Altaris announced that the Hart-Scott-Rodino antitrust waiting period has expired for its pending acquisition of Simulations Plus, Inc. (Nasdaq: SLP), clearing a key antitrust condition.
  • The HSR expiration was disclosed in an 8-K filing dated August 13, 2026.
  • Two conditions still remain: approval by Simulations Plus shareholders and certain regulatory approvals in France.
  • Subject to satisfaction or waiver of the remaining conditions, the deal is expected to close in the second half of calendar 2026.
  • Altaris is a New York-based, healthcare-focused firm managing more than $9 billion in equity capital that has invested in more than 50 healthcare companies since 2003.

Healthcare private equity has been moving at a deliberate pace through this stretch of the deal cycle, and the regulatory calendar for software-driven biopharma tools is now moving to match. Altaris, the New York-based investment firm managing more than $9 billion in equity capital with a focus exclusively on healthcare, announced Wednesday that the Hart-Scott-Rodino waiting period has expired for its pending acquisition of Simulations Plus, Inc. (Nasdaq: SLP), clearing one of the key antitrust conditions standing between the two parties and a completed transaction.

The expiration was disclosed in an 8-K filing dated August 13, 2026. The Hart-Scott-Rodino Antitrust Improvements Act of 1976 sets the standard antitrust review mechanism for deals of this scale, and its clearance moves the transaction to its remaining gates. Two conditions still stand. Simulations Plus shareholders must vote to approve the merger. The company must also obtain certain regulatory approvals in France. Both are described in the filing as customary closing conditions, and subject to their satisfaction or waiver, the deal is currently expected to close in the second half of calendar 2026.

Sector context and the cross-border close

Simulations Plus describes itself as a global leader in model-informed and AI-accelerated drug development, offering software and consulting to biopharma clients globally to accelerate drug discovery, development, and commercialization. The company is based in Research Triangle Park, North Carolina. That category of work has attracted sustained capital interest, a trend Altaris's own record reflects: the firm has invested in more than 50 healthcare companies across subsectors since its inception in 2003, with an exclusive focus on healthcare. Acquiring SLP fits within that stated mandate.

The French regulatory approval requirement is the most unpredictable element that remains. Cross-border sign-off can move independently of any timetable the parties set, and the demand environment for regulatory clearance in Europe shifts with trade and policy conditions. On balance, Wednesday's HSR expiration removes one obstacle from a transaction still subject to a shareholder vote and a regulatory process that crosses borders. As of the August 13 filing, both remain open.

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Frequently asked

Who is acquiring Simulations Plus?

Altaris, a New York-based investment firm focused exclusively on healthcare and managing more than $9 billion in equity capital, is acquiring Simulations Plus, Inc. (Nasdaq: SLP).

What conditions still need to be met before the deal closes?

Simulations Plus shareholders must vote to approve the merger, and the company must obtain certain regulatory approvals in France, both described as customary closing conditions.

When is the acquisition expected to close?

Subject to satisfaction or waiver of the remaining conditions, the transaction is currently expected to close in the second half of calendar 2026.

What does Simulations Plus do?

Simulations Plus, based in Research Triangle Park, North Carolina, describes itself as a global leader in model-informed and AI-accelerated drug development, offering software and consulting to biopharma clients to accelerate drug discovery, development, and commercialization.

Why is the French regulatory approval significant?

The French regulatory approval is described as the most unpredictable remaining element because cross-border sign-off can move independently of the parties' timetable and shifts with trade and policy conditions.