Mindlance Clinical Monitoring provides professional oversight services to the pharmaceutical, medical device, and biotechnology industries. At Mindlance Clinical our focus is always on the needs of our customers.

We have developed a truly regional approach to the regional monitoring function. This considerably reduces travel expense, burnout, and training costs and allows for a more experienced staff due to lower turnover. The Mindlance Clinical Monitoring model is streamlined, professional, and cost-effective.We have enlisted experts in a broad range of therapeutic areas and all clinical phases to provide complete coverage by experienced professionals throughout your entire drug development process.

Mindlance Clinical Monitoring allows you the flexibility to keep control over the monitoring process while providing you greater value for your investment. The clinical trials process is an integral part of bringing a compound to market and Mindlance Clinical can help you reach a successful conclusion.

Monitoring offerings:

• Pre-Study Visits
• Site Initiation Visits
  
• Routine Monitoring Visits
• Close-Out Visits
• Clinical Supply Management
• Essential Document Management
  
• Trip Report Review Tracking
• Co-Monitoring
  
• Data Management
• Query/Addenda Resolution
• CRF Review
• Project Management