Project Management–Sponsor relationships are essential to us. For that reason, a single point of contact is assigned to each sponsor to ensure the quality of our communication and the relationships we develop. Principal contacts are professionals with scientific training, experience, and project management skills. They are adept at communicating both technical and management issues with sponsors.

 

Quality Compliance–All of our bioanalytical 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 at each site. Study data and reports are thoroughly reviewed before receiving our quality assurance seal.

 

Scientific Affairs–Our experienced team of scientists integrates innovation, expertise, and new information to optimize the development of a new drug for approval.

 

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.