Over the past 18 years, Pharmatech has worked and continues to work as a traditional CRO and SMO within the pharmaceutical and biotechnological industries. Pharmatech’s unique network approach, flexible service package, and updated document collection, all position Pharmatech as unparalleled in the industry.

As a benefit of working with Pharmatech, sponsors gain access to our biggest asset: Research Networks.
Network focused research allows for access to over 1 million patients annually, experienced community-based physicians, and centralized research development and management services.  Pharmatech offers industry sponsors a variety of research management services.  Traditional contract research and site management services are deployed through the organized research networks:

Site Management Organization (SMO)

• Project and Site Feasibility
• Site Identification, Selection, and Management
• Management of Regulatory Documents
• Grant Management
• Centralized Contracting
• Enrollment Support

Clinical Research Organization (CRO)

• Protocol Development
• CRF Design
• Data Collection/Statistical Analysis
• Monitoring
• Medical Publication and Reporting
• Communication Tools

Pharmatech is uniquely positioned in the field of oncology research with a strong focus on community-based oncologists participating in Phase III and Phase IV trials where the pharmaceutical companies need support to reach large patient numbers.  Pharmatech values the relationships we build with each sponsor and we strive to manage our objectives through key performance metrics:

• Project Starts – We strive to have patient enrollment begin within six weeks from signing a contract with a Sponsor company.
• Patient Enrollment – We strive to have 120% of our patient enrollment reached in 80% of the time allotted for the project.
• Patient Safety – The patients’ safety is paramount; it is the most important aspect in clinical research.
• Data Quality

• Proper Informed Consent must be obtained for each patient
• Inclusion and Exclusion criteria must be met for each study patient
• Primary endpoints of the study must be obtained
• All dispensed drugs are recorded to assure proper drug accountability
• Safety data must be accurately recorded to meet the objectives of the trial

Click here to view a detailed list of sponsor services.

To obtain more information about our services, please contact us.