Horsham, Pennsylvania – December 21, 2009: Liquent, Inc. (“Liquent”), a provider of software and service solutions designed to support the regulatory business processes of life sciences companies, announced that it has been acquired by Marlin Equity Partners (“Marlin”) from Thomson Reuters.
Based in Los Angeles, CA, Marlin is a leading private investment firm with over $1 billion of capital under management. Liquent is the provider of Liquent InSight®, a fully integrated and scalable regulatory information management platform. InSight can be leveraged throughout a client organization in support of a life sciences company’s development, registration, and manufacturing processes. Through its Regulatory and Clinical Services consulting services team, Liquent also provides a full range of outsourcing services to support the regulatory submission and registration management activities of a life sciences company.
Liquent’s current General Manager, Rick Riegel, will continue his leadership position as the CEO of the company. “We are very excited to be partnering with such a strong private equity firm,” commented Rick Riegel. “Marlin brings substantial financial resources and expertise in the healthcare IT sector. With their backing and Liquent’s comprehensive software and service solutions, industry leadership, and focus on customer service, we look forward to accelerating our growth and ability to service the evolving and rapidly changing needs of the life sciences industry.”
“Marlin recognizes the life sciences industry’s constant struggle with regulatory change, new product approvals, and cost pressures. Marlin’s backing combined with Liquent’s software and outsourcing capabilities positions us well in helping our customers solve complex regulatory challenges,” stated Jim Brady, Healthcare Operating Partner at Marlin Equity Partners.
Behind the Buzz: Why Clinical Research Leaders Flock to SCOPE Summit
February 7th 2025In this episode, we meet with Micah Lieberman, Executive Conference Director for SCOPE Summit (Summit for Clinical Ops Executives) at Cambridge Innovation Institute. We will dive deep into the critical role of collaboration within the clinical research ecosystem. How do we bring together diverse stakeholders—sponsors, CROs, clinical trial tech innovators, suppliers, patients, sites, advocacy organizations, investors, and non-profits—to share best practices in trial design, program planning, innovation, and clinical operations? We’ll explore why it’s vital for thought leaders to step beyond their own organizations and learn from others, exchanging ideas that drive advancements in clinical research. Additionally, we’ll discuss the pivotal role of scientific conferences like SCOPE Summit in fostering these essential connections and collaborations, helping shape the future of clinical trials. Join us as we uncover how collective wisdom and cross-industry partnerships are transforming the landscape of clinical research.
SOUL Trial Shows Oral Semaglutide Significantly Reduces Cardiovascular Risk in Type 2 Diabetes
April 3rd 2025Phase III SOUL trial shows daily oral semaglutide lowers the risk of major adverse cardiovascular events in patients with type 2 diabetes and atherosclerotic cardiovascular disease or chronic kidney disease, with benefits consistent with injectable semaglutide and other GLP-1 receptor agonists.
Reaching Diverse Patient Populations With Personalized Treatment Methods
January 20th 2025Daejin Abidoye, head of solid tumors, oncology development, AbbVie, discusses a number of topics around diversity in clinical research including industry’s greatest challenges in reaching diverse patient populations, personalized treatment methods, recruitment strategies, and more.