A COMPREHENSIVE BOOTCAMP TO SITE EXCELLENCE

Our intensive bootcamp provides struggling clinical trial sites a path to excellence through hands-on intervention and ongoing support. Sites grappling with major-to-severe protocol deviations, GCP compliance issues, staffing problems or inadequate infrastructure attend an initial multi-day in-person workshop at the site's location for rapid rehabilitation. An internal audit review of current processes and performance is conducted to identify priority areas for improvement. Targeted training and customized recommendations then enable sites to boost competence, compliance and quality operations.

Areas covered are based on a per site basis but are inclusive of the following:

• Comprehensively build site capabilities spanning from rectifying protocol deviations
• Dramatically improving recruitment and retention metrics
• Transforming disjointed workflows into seamless integrated systems/processes
• To completely revolutionizing accountability regarding stringent investigational product handling per evolving Global trial administration standards.

Sites receive toolkits with actionable strategies which are reinforced through regular remote follow-up guidance to drive change management. The objective is equipping sites to reach and sustain operational best practices for conducting and managing research.

By the program’s conclusion, sites undergo a final assessment confirming they have the disciplined protocols, personnel and performance monitoring needed for long-term clinical trial reliability and regulatory standards alignment.

Hands-On Training

GCP Compliance

Internal Audits

Dedicated Support

OUR RESCUE APPROACH

Sites Battling Protocol Deviations, Recruitment Challenges or Regulatory Non-Adherence: Stop the Struggle - Our Immersive Bootcamp Fortifies Long-Term Clinical Trial Competency Within Weeks