Welcome to our dedicated page for Iqvia Hldgs news (Ticker: IQV), a resource for investors and traders seeking the latest updates and insights on Iqvia Hldgs stock.
IQVIA Holdings Inc. (NYSE: IQV) is frequently in the news as a global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. News coverage about IQVIA highlights how the company combines high-quality health data, Healthcare-grade AI®, advanced analytics and technology to support clinical development and commercial decision-making.
On this page, readers can follow IQVIA news related to clinical research initiatives, technology launches and strategic partnerships. Recent announcements include a strategic collaboration with Amazon Web Services, under which AWS has been named IQVIA’s Preferred Agentic Cloud Provider to power a next-generation AI platform. Other news items describe the launch of IQVIA’s Clinical Trial Financial Suite, an AI-enabled platform for managing financial aspects of clinical trials, and partnerships with organizations such as Veeva Systems.
IQVIA news also covers topics such as quarterly financial results, leadership and board changes, awards for site relationships in clinical research and the expansion of clinical research networks. For example, the company reports on its Research & Development Solutions bookings and backlog, as well as its recognition with the WCG Pinnacle Award for Site Relationships in Professionalism and Communication.
Investors, researchers and industry professionals can use this news feed to monitor developments in IQVIA’s clinical research services, healthcare analytics capabilities, AI initiatives and collaborations across the life sciences ecosystem. Regularly reviewing IQVIA news can provide insight into how the company is applying data, analytics and technology to support the development and commercialization of medical treatments.
IQVIA (NYSE:IQV) and Veeva Systems (NYSE:VEEV) have announced comprehensive global partnerships in clinical and commercial domains, alongside resolving all pending legal disputes. The long-term agreement enables seamless integration of both companies' software, data, technology, and services.
The partnership encompasses two key areas: Commercial collaboration, establishing master data and third-party access agreements for mutual data usage across platforms, and Clinical integration, with IQVIA joining Veeva's CRO Clinical Data Partner program to leverage the Veeva Clinical Suite for clinical trials execution.
The collaboration aims to enhance customer efficiency by streamlining product integration and accelerating clinical development processes, database builds, study locks, and data delivery.
Veeva Systems (NYSE:VEEV) and IQVIA (NYSE:IQV) have announced comprehensive global partnerships in clinical and commercial domains, alongside resolving all pending legal disputes. The long-term agreement enables seamless integration of both companies' software, data, technology, and services.
The commercial partnership establishes master data and third-party access agreements, allowing mutual data usage across platforms including Veeva Network, Veeva Nitro, and Veeva AI. IQVIA has joined multiple Veeva partner programs to support customer integrations. In the clinical domain, IQVIA's participation in Veeva's CRO Clinical Data Partner program will facilitate clinical trials execution using Veeva's software products, particularly in EDC (Electronic Data Capture) implementations.
IQVIA (NYSE:IQV) reported strong Q2 2025 financial results with revenue reaching $4,017 million, up 5.3% year-over-year. The company's Technology & Analytics Solutions (TAS) segment showed robust performance with 8.9% growth to $1,628 million.
Key highlights include GAAP Net Income of $266 million, Adjusted EBITDA of $910 million, and Adjusted Diluted EPS of $2.81. R&D Solutions achieved quarterly bookings of $2.5 billion with a book-to-bill ratio of 1.12x and a contracted backlog of $32.1 billion. The company repurchased $607 million of common stock in Q2.
IQVIA updated its full-year 2025 guidance, projecting revenue between $16,100-16,300 million and Adjusted EBITDA of $3,750-3,825 million.
IQVIA (NYSE:IQV), a leading global provider of clinical research services, commercial insights and healthcare intelligence, has scheduled its second-quarter 2025 financial results announcement for Tuesday, July 22, 2025, before market opening.
The company will host a conference call and webcast at 9:00 a.m. Eastern Time on the same day. Management will discuss the quarterly results, which will be available on IQVIA's Investor Relations website. Interested participants must register in advance to join the conference call, and a webcast replay will be accessible approximately two hours after the event.
Rein Therapeutics (NASDAQ: RNTX) has announced the dosing of its first patient in the RENEW Phase 2 trial of LTI-03, targeting idiopathic pulmonary fibrosis (IPF). The trial will evaluate the safety, tolerability, and efficacy of LTI-03, a novel Caveolin-1-related peptide treatment.
The study is designed as a multi-center, randomized, double-blind, placebo-controlled trial that aims to enroll 120 patients across 50 global sites. Participants must have been diagnosed with IPF within 5 years of screening. The trial's primary endpoint focuses on treatment-emergent adverse events through Week 24, while secondary endpoints measure efficacy through FVC, ppFVC, and HRCT metrics. Rein is collaborating with IQVIA for enrollment, and topline interim data is expected in H1 2026.
IQVIA (NYSE:IQV) has announced a strategic collaboration with SCRI Development Innovations, the contract research organization arm of Sarah Cannon Research Institute, to enhance global oncology trials. The partnership combines IQVIA's global reach and expertise in managing one-fifth of U.S. oncology trials with SCRI's community oncology experience and Accelero operational model.
The collaboration aims to streamline clinical trial processes, reduce operational barriers, speed up data delivery, and accelerate the development of new cancer therapies. SCRI's Accelero model facilitates faster trial activation, improved recruitment, and seamless integration of electronic health records with data capture systems for U.S. clinical trials.