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  • PROGRAM, PROJECT MANAGEMENt

  • Pre-Approval Inspection  Preparation

  • Budget Projections and   Oversight

  • Resource Planning

  • Study Document              Development

  • MONITORING

  • data management

  • TRIAL MASTER FILE 

  • CODING

  • BIOSTATISTICS

  • SAFETY

  • Clinical Data Review and Cleaning

  • Quality and Risk Assessments

  • Technical Writing

  • Regulatory Submissions

  • ....& more

SUPPORTING CLINICAL TRIAL PERSONNEL

 

Haversac partners with clinical trial research professionals to provide study role services to the trial industry at greater combined quality and proficiency levels.  Our research partners remain independent while Haversac's administrative staff support and enhance the team's performance using Haversac Ticket™ : A secure online item-issue repository, communication, and management application.

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Our study role teams assume responsibility for capturing, time-stamping, tracking, documenting, measuring, and closing its related item-issues. Haversac Ticket administrators remain knowledgeable while keeping item-issues current so substitution of our research partners is efficient if needed. In addition, our clients access Haversac Ticket to monitor performance and download its content for master record keeping.

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