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About the Authors:
Joseph Munda
Managing Director
Joe Munda has worked in finance and investment for 18 years and joined First Analysis in 2015. He works with entrepreneurs as an investor and as an advisor on growth transactions to help build leading businesses in healthcare technology. He has played a key role in building First Analysis' franchises in drug development technology and medical technology and has published several thought-leading white papers in those areas. He supports First Analysis' investments in Applied StemCell, Checkpoint Surgical, Medicinal Genomics, Sware, Transformative Pharmaceutical Solutions, VIDA Diagnostics and Yunu. Prior to joining First Analysis, he was an equity research analyst covering medical device and healthcare services companies at Sidoti & Co. Earlier, he worked in institutional sales at Bear Stearns/J.P. Morgan. He earned a bachelor's degree in finance from Fairleigh Dickinson University.
Walid Elmekki
Associate
Walid Elmekki is an associate with First Analysis. Walid joined the firm in 2021 after completing his internship. He previously interned at Wintrust Financial supporting the commercial banking division. Walid graduated from Ohio State University with a bachelor’s degree in finance and a certificate of leadership.
First Analysis Pharma IT Team
Joseph Munda
Managing Director
Matthew Nicklin
Managing Director
Tracy Marshbanks
Managing Director
Andrew Walsh
Managing Director
Walid Elmekki
Associate
First Analysis Quarterly Insights
Pharma IT
What the second Trump term could mean for pharma IT
March 18, 2025
  • We explore the potential impact of Trump’s second term on three aspects of the pharma sector and what the changes might mean for pharma IT.
  • First, we expect pharmaceutical benefit managers (PBMs) to face continued scrutiny from Trump’s incoming FTC chairman, Andrew Ferguson, as part of Trump’s initiative to reduce drug prices. Potential impacts on pharma IT companies include increased opportunities for companies providing solutions for health economic outcomes research, real-world evidence and patient reported outcomes.
  • Second, we expect the Trump administration to continue its push for expedited drug approvals and funding and tax incentives for research and development, while increasing use of artificial intelligence in drug discovery and development and emphasizing post-market surveillance to monitor patient outcomes. Potential impacts on pharma IT companies include increased opportunities for those focusing on real-world evidence and pharmacovigilance data as well as those focused on streamlining processes for collecting data and submitting it to the FDA.
  • We expect the administration’s focus on bolstering domestic manufacturing and reducing U.S. reliance on foreign supply chains to lead to renewed interest in onshoring drug development and manufacturing by both pharma companies and contract development and manufacturing organizations. Potential impacts on pharma IT companies center around opportunities in supply chain logistics.

TABLE OF CONTENTS

Looking beyond vaccines: Three key areas to focus on

Renewed focus on drug pricing

Accelerated drug approvals and regulatory reforms

Emphasis on domestic manufacturing

Change likely to create new opportunities

Pharma IT indexes down year-over-year

Pharma IT M&A: Notable transactions include Greenphire and BuildClinical

Pharma IT private placements: Notable transactions include Aqemia and Manas AI

Looking beyond vaccines: Three key areas to focus on

Donald Trump’s return to the presidency has generated a mix of optimism and uncertainty in the pharmaceutical industry. While much of the public discussion has focused on Trump’s selection of Robert F. Kennedy Jr. as secretary of the Department of Health and Human Services and his potential impact on vaccines, in this report we focus on other areas including drug pricing, regulatory reforms and manufacturing, and trade policies to assess the potential impact of Trump’s second term on the pharma sector and what the changes might mean for pharma IT.

Renewed focus on drug pricing

A primary concern for the pharmaceutical sector is the administration’s commitment to lowering drug prices and increasing price transparency. During his first term, Trump proposed several policies aimed at reducing the cost of prescription drugs. These included efforts to negotiate drug prices for Medicare, reform the pharmacy benefit manager (PBM) system, and implement international pricing reforms. Trump’s “America First” healthcare plan included provisions aimed at lowering drug costs by enabling Medicare to negotiate directly with pharmaceutical companies, an effort to make the system more transparent and competitive.

This last initiative (the biggest pharmaceutical regulation change in several years) came to fruition under the Biden administration’s Inflation Reduction Act (IRA) of 2022, which granted Medicare authorization to negotiate prices for its costliest prescription drugs. Prices for the first ten Medicare-negotiated drugs were released last August and are expected to go into effect in 2026. Although it’s unclear whether the Trump administration supports this change as it was laid out in the IRA, the Centers for Medicare and Medicaid Services recently announced plans to proceed with negotiating Medicare prices for the next 15 drugs selected under the IRA, listed in Table 1.

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