Research Management

CiPharma provide management  and support of research sites both domestic and offshore. With a strong focus on compliance requirements and site knowledge, we ensure studies are conducted to the highest standards of quality and compliance.

Research Expertise and Reach

Our services footprint encompasses domestic core markets and extends to the Indian sub-continent and Africa. We draw on, train and support highly skilled country specific resources providing local expertise to execute clinical projects of any size.

Our processes include site qualification on a 186 point inspection survey. CiPharma manage and support specialists including investigators with expertise across all therapeutic areas the majority of whom have successfully completed trials with retention rates of between 90 to 95{4d872c21a69961dfdde9c12c1b4f1b14a75ed06c709f453dbea861529fa2e0cc}.

Trial Management

Sponsor companies and research organizations receive assistance with all aspects of planning, placing and conducting clinical trials. Solutions are customized to fit the specific needs of each client’s study. CiPharma train and support your organization across all key areas including:

  • Study feasibility analysis
  • Principal investigator and site selection
  • Document collection and management
  • Placement of highly trained, dedicated coordinators
  • Investigator and coordinator training programs
  • Pro-active patient recruitment and retention programs
  • Strong track record of data quality and integrity

Regulatory Support

The management team has in-depth regulatory experience that assures correct submission and rapid regulatory approval:

  • Submissions to the IRBs, ethics committees and national regulatory agencies.
  • Regulatory approval in 6-8 weeks and start-up within 12-16 weeks