THERAPEUTIC
EXPERTISE
DEVELOPMENT
PLAN
PHASE I
PHASE II-III
REGULATORY SUBMISSION
POST-MARKETING
STUDIES
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.
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.
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.
Clinical Development Strategies
Clinical Trial Design
R&D Management Consulting
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
Development Plan
Phase I
Phase II–III
Phase IIb/III Study Delivery
Protocol Validation
Clinical Monitoring
Global Laboratories
Patient Recruitment
Regulatory Submission
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.
Post-Marketing Studies
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.
LEARN MORE
LEARN MORE
LEARN MORE
LEARN MORE
THERAPEUTIC
EXPERTISE
Explore our Services
Click to learn more
