About Clinipace Worldwide
As a digital CRO (dCRO), Clinipace pioneered an innovative service model to transform drug and medical device development by delivering technology-amplified services to improve performance, collaboration, and visibility across all stakeholders. While similar in many ways to a traditional CRO, Clinipace is uniquely built to deliver:
- An innovative methodology that reduces clinical development cost and budget volatility
- A streamlined, efficient operational approach that delivers the right infrastructure and resources
- An expert global regulatory team to set you on the right path
- Experienced, therapeutically-focused clinical development staff organized specifically for emerging and mid-tier firms
- A user-friendly trial and data management platform that delivers real-time visibility and project control built on an affordable and highly available infrastructure
Powered by TEMPO™ – our proprietary eClinical technology – our teams ensure your success and bring unsurpassed efficiency and quality to your development programs. It’s the integrated approach combining technology and study execution that improves performance, visibility, and coordination for all stakeholders, and it’s a vital part of the culture at Clinipace Worldwide.
As an innovative dCRO, we improve the way contract research is performed. To achieve this, we deploy proprietary technology that enables our project teams to conduct our clients’ regulatory and clinical development programs to the highest levels of quality and efficiency.
Clinipace Worldwide values transparency, integrity and a performance-oriented culture. These core values drive service quality and delivery, resulting in profitability and sustainability for the benefit of our employees, customers, and shareholders.