Regulated Content Management Services
- Clinical Development Strategies
- Clinical Trial Design
- 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
- Patient Centered Endpoints
- Regulated Content Management Services
- Site Relationships and Networks
- Therapeutics & Specialty Expertise
- Wearables & Connected Devices
Improved productivity and better collaboration. Compliantly.
IQVIA’s Wingspan Content Management solutions help make your users more efficient by automating processes and reducing steps—while at the same time complying with the requirements of Health Authorities worldwide.
Whether you are a small CRO, a biotech at pre-commercialization, or a Top 10 pharma our experienced resources can support your content management needs. And, with an affordable pricing model that includes installation, validation, a User Acceptance Test package, training and all upgrades there’s no surprises. Our approach provides you with:
- Superb performance delivered across the globe, monitored constantly by our team
- Client-driven, first-to-market feature enhancements –activated on your schedule
- Expert advice and assistance –ongoing support, even after you go into production
So even when budgets are tight, IQVIA can offer an easier way to improve productivity, compliance, and collaboration.
Find out more about how IQVIA’s Wingspan Content Management solutions can help you succeed.