- Clinical Development Strategies
- Clinical Trial Design
- Protocol Validation
- Customized R&D Capabilities
- Early Clinical Development
- Full Service R&D Capabilities
- Functional Service Provider Capabilities
- Global Laboratories
- Investigator Information
- Patient Recruitment
- Patient Retention
- Phase IIb/III Study Delivery
- R&D Management Consulting
- Site Relationships and Networks
- Therapeutics & Specialty Expertise
- Wearables & Connected Devices
To reach the right outcome, start from the right place
Precision. Clarity. Consistency. When you’re investing millions in developing a new drug, you need to have confidence that your protocol is rock solid. That it will perform as expected in the clinic, where changing standards of care, competition for patients, and costly protocol amendments are all too common.
By working with IQVIA from the start, you can reduce your risk and increase predictability by validating your protocols against real-world data.
- Test for patient and site burden to identify barriers to patient recruitment and retention
- Identify non-core procedures to save money and time
- Understand your competitors to benchmark design and enrollment strategies
- Improve your eligibility criteria for finding eligible patients and predicting screen failure
Before your start your study, pressure test your protocol.