PharmaNet’s global resources comprise a network of more than 2,500 professionals
in 40 locations around the world. Included in these locations are 3 clinical facilities
available through Anapharm, our Canadian-based subsidiary. Anapharm’s modern,
well designed and spacious clinics offer a capacity of more than 500 beds divided into
12 independent units, 40+ physicians, and 400+ support staff.

 

We apply a superior methodology to ensure the efficiency, integrity, and value in every program we conduct. Key elements of our methodology include:

 

Sponsor Relationships–We engage in a unique program of continual assessment and improvement that builds cooperative relationships among project teams, including members representing both PharmaNet and our sponsors.

 

Senior-Level Management Oversight–We provide senior-level managers who are actively engaged and directly accessible throughout projects to help avoid and immediately address any issues that may arise.

 

Project Management–We consider our core competency to be project management. We set industry standards for the quality of our professionals, the tools they use, and the strategies and efficiencies they bring to managing their projects. For early phase programs, a project manager (PM) is assigned to each sponsor to ensure the quality of our communication and the relationships we develop. Our PMs are expert clinicians who work in close cooperation with a select medical/scientific team to keep sponsors informed on the progress of their program.

 

Quality Compliance–All of our early phase departments, including data processing and report writing, comply with current standards for Good Clinical Practices and Good Laboratory Practices. An independent quality-assurance unit is an integral component in every project team. Study data and reports are completely validated before receiving our quality assurance seal.

 

Scientific Affairs–Our experienced team of scientists integrates innovation, expertise, and the most-current information to optimize both the development of new drugs and the bioequivalence-testing of generic drugs.

 

Regulatory Affairs–Our in-house team of experienced professionals can list the requirements and chart a timeline to help you navigate the intricate path of global regulation.

 

Regulatory Audit–Our procedures, facilities, and projects are routinely audited by international agencies.