Post-Approval & Registry Solutions

Solving Real Problems. Getting Real Results.

Clinipace offers an integrated clinical data capture and study management platform to streamline the research process surrounding post-approval research and registries by eliminating the integration headaches associated with multiple platforms, reducing project efforts and costs from startup to conclusion, and empowering project stakeholders to make informed real-time decisions regarding their research.

Many Demands. One Platform.

We know one size does not fit all studies. That’s why we’ve concentrated our focus on making TEMPO the most scalable and flexible combination of clinical data capture and study management tools in the market.

With TEMPO, biopharmaceutical and medical device companies, CROs an AMCs have a fully integrated platform to successfully conduct studes that yield a wealth of information from physicians practicing in real-world settings. The outcomes are many, including:

• Meeting post-approval regulatory requirements
• Meeting safety and effectiveness standards
• Generating product experience data from a real-world setting
• Tracking drug, patient and disease outcomes