Learn more
TM
TM
Through the interconnected capabilities of the IQVIA CORE, our scientific and operational teams can bring your clinical development program into the next generation. Real world insights are integrated throughout design and delivery to achieve new levels of precision, efficiency, and predictability.
Powered by the IQVIA CORE
Learn more
Regulatory authorities are now increasing opportunities for you to provide real-world evidence of your products’ safety and effectiveness. This changing environment can make your products more available to patients.
Post-marketing Studies
Learn more
Tap into IQVIA’s extensive regulatory expertise to confidently interact with regulatory authorities around the world. Our team of medical writers, biostatisticians, regulatory specialists and subject matter experts work together to deliver faster, more efficient submissions with the quality you need.
REGULATORY SUBMISSION
Patient Recruitment
Global Laboratories
Clinical Monitoring
Protocol Validation
Phase IIb/III Study Delivery
You can trust IQVIA to deliver your Phase II-III trials with quality, speed and efficiency. With experts across a complete range of clinical trial services and trial experience in 100+ countries, we can help you achieve your study’s goals.
Phase II-III
Learn more
IQVIA is with you from the start, with expertise in complex early clinical studies, a global network of highly qualified Phase I units, and innovative data-driven approaches to accelerate proof of concept.
PHASE I
R&D Management Consulting
Clinical Trial Design
Clinical Development Strategies
Bring real-world and commercial insights into your clinical development planning. Discover alternative paths and study designs that shorten timelines, decrease costs, and maximize your asset value.
DEVELOPMENT PLAN
Learn more
Looking for shared passion and a team that’s been there before? IQVIA delivers, through a deep bench of therapeutic experts who also deliver valuable insights on the clinical and commercial landscape for your disease area. Our experienced study teams know what to expect and how to help you reach success.
THERAPEUTIC EXPERTISE
Explore our services
Roll over each section to learn more.
Development
Plan
Phase I
Phase II-III
Regulatory
Submission
Post-marketing
Studies
Therapeutic Expertise
Powered by
The IQVIA CORE
TM
Therapeutic Expertise
Development
Plan
Phase I
Phase II-III
Regulatory
Submission
Post-marketing
Studies
Powered by
The IQVIA CORE
TM