Clinical Research

To ensure accuracy and efficiency we provide high quality trial logistics in: 

  • Site initiation to trial close-out operations

  • Patient recruitment

  • Standard operating procedures development

  • Maintenance and archival of trial-related documents

  • Information Technology solutions

  • Data management 

  • Quality assurance

  • Protocol Monitoring 

  • Ethics Submissions


In addition to site management services we offer:

  • ICH-GCP training

  • Clinical Research Associate training

  • Clinical Research Coordinator training

Clinical Trial Site Management:
We offer comprehensive services in clinical trial development, data management and regulatory affairs. Our team is well versed in FDA CFR 21, Health Canada, and  EMEA regulations as well as those of other regions and countries.

Current studies:
Client: Womens' Health Association of Kenya
Study: Women's Knowledge on Menopause in an Urban Setting: Nairobi, Kenya
Description: Cross-sectional descriptive study on the current state of knowledge of menopause by  40 - 60 year old women.
Solutions: Protocol development, regulatory affairs, patient recruitment, data management, quality control, data analysis