Clinical
PharPoint Research Clinical Operations is able to provide comprehensive clinical services in support of your clinical research project needs. Clinical activities are tailored to the individual sponsor’s requirements and staffed with highly qualified clinical research professionals. Our clinical operations staff focus on ensuring sites carefully follow the investigational plan and provide our sponsors with greater confidence about human research subject protection throughout the research. Throughout the project, our clinical research professionals use effective interactions with investigational site staff to increase efficiency and provide for accurate and reliable data from which to build your clinical program. By use of this model, our teams can take your program from Phase I through NDA.
Our clinical operations services include the following:
- Project Management
- Clinical Monitoring
- Site Feasibility Assessments
- Investigator Meeting Preparation and Presentations
- Study Start Up Support / Essential Document Review and Processing
- Site Management and Communication Production
- Vendor Management (Laboratories, Clinical Trial Material Supplies and Packaging)
- IVRS Vendor Selection and Oversight
- Clinical Trials Management System (CTMS)
- Functional Outsourcing
- Investigator Grant and Research Budget Preparation and Administration
Clinical Force
The Clinical Force provides PharPoint Clinical Services with the perfect clinical trial management system. Clinical Force CTMS has a secure and stable structure to the complex and changing clinical trial process. Clinical Force combines ease of use, extensive functionality and an inventive set of features to allow PharPoint to better manage, track and report on our sponsor’s clinical trial. With the system’s web-based project portal, PharPoint clients can get up-to-date information on their project’s status, allowing for informed decisions as to the conduct of their clinical trials.
