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Delta Pharma Monitoring
provides professional oversight services to the
pharmaceutical, medical device, and biotechnology
industries. At Delta 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 Delta Pharma 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.
Delta Pharma 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 Delta Pharma
can help you reach a successful conclusion.
• 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
• Study Rescue
Download
a printable One Page Marketing Brochure
about Delta’s Clinical Monitoring Practice.
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