Harness the power to transform clinical development
Reimagine clinical development by intelligently connecting data, technology, and analytics to optimize your trials. The result? Faster decision making and reduced risk so you can deliver life-changing therapies faster.
Real World Evidence. Real Confidence. Real Results.
Generate and disseminate evidence that answers crucial clinical, regulatory and commercial questions, enabling you to drive smarter decisions and meet your stakeholder needs with confidence.
Service driven. Tech-enabled. Integrated compliance.
Orchestrate your success across the complete compliance lifecycle with best-in-class services and solutions for safety, regulatory, quality and medical information.
By making intelligent connections between your needs, our capabilities, and the healthcare ecosystem, we can help you be more agile, accelerate results, and improve patient outcomes.
Building on a rich history of developing AI for healthcare, IQVIA AI connects the right data, technology, and expertise to address the unique needs of healthcare. It's what we call Healthcare-grade AI.
Your new expert analyst is here. Be at the forefront of data-driven decision-making with a new generative AI tool that enables you to interact with our products and solutions like never before. Get results you can trust, faster.
Your healthcare data deserves more than just a cloud.
The IQVIA Human Data Science Cloud is our unique capability designed to enable healthcare-grade analytics, tools, and data management solutions to deliver fit-for-purpose global data at scale.
Innovations make an impact when bold ideas meet powerful partnerships
The IQVIA Innovation Hub connects start-ups with the extensive IQVIA network of assets, resources, clients, and partners. Together, we can help lead the future of healthcare with the extensive IQVIA network of assets, resources, clients, and partners.
IQVIA Decentralized Trials deliver purpose-built clinical services and technologies that engage the right patients wherever they are. Our hybrid and fully virtual solutions have been used more than any others.
In the pre-clinical phase, accurate documentation is vital for regulatory submissions and study approvals. Our team can assist with:
Protocol Translations: Ensuring study protocols meet regulatory requirements across regions.
Investigator Brochures: Providing precise translations for investigators.
Ethics Committee Correspondence: Facilitating clear communication to obtain approvals and address concerns.
Accurate and consistent translations for multinational studies.
Clear translations to ensure patient understanding.
Effective translations to engage diverse populations.
Precise translations to comply with local and international regulations.
Timely translations to maintain compliance and patient safety.
Easy-to-understand summaries of study results for participants.
Validating translations to ensure cultural and linguistic appropriateness of Clinical Outcomes Assessments (COA).
IQVIA Language Solutions
Execute your global clinical trials with precision
While providing reliable language accuracy and the highest level of security and compliance, our life sciences solutions to are designed to help you overcome language, cultural, and accessibility barriers in clinical trials while accelerating patients access to innovative medicines.
25%
Reducing cost of clinical translation Project delivered for a top pharma client
300%
more stringent quality indices compared to legacy language models
14,000
Informed Consent Forms and Protocols Translated in 2024
Learn more on the importance of linguistic validation, a critical step in the development and execution of clinical trials, particularly those that involve multinational and multicultural patient populations.