CPP Inc

Our results-driven service offerings help sponsors and CROs:

• Predict, manage and accelerate clinical trial timelines
• Develop more "implementation friendly" protocols
• Make informed site selection decisions
• Validate enrollment potential
• Create, diagnose, troubleshoot and rejuvenate recruitment and retention plans
• Collect, manage, use and interpret practical study and site performance metrics
• Manage sponsor-site relationships more effectively
• Train their staff and sites in more effective means to manage protocol implementation challenges and enhance subject participation in clinical trials

With over 25 years of healthcare and clinical research experience, our key strengths include:

• Unparalleled ability to efficiently and thoroughly dissect a protocol to understand and map out the barriers and opportunities impacting study enrollment
• Creative thinking skills combined with evidence-based methodology that enables the development of innovative yet practical solutions to accelerate recruitment
• Thorough understanding of effective recruitment and retention strategies and tactics that can be applied across multiple therapeutic areas, countries, cultures and various site operating models
• Expert analytical skills to understand and interpret the effectiveness of various approaches to accelerating the clinical trials process
• Extensive hands-on experience implementing clinical trials and interacting with investigators, study coordinators and research personnel, with an in-depth understanding of the characteristics that predict successful site performance
• Skilled trainer with a passion for sharing successful practices and unique ability to enhance knowledge transfer through practical and interactive learning activities with multi-cultural audiences