Clinwatch Research Services

As a CROs we support foundations, research institutions, and universities, in addition to governmental organizations. We have expertise in site management, clinical research, clinical trials management, and pharmacovigilance.

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Our clinical trial solutions span the following:

Site selection & assesent
Our site selection and assessment services include:
  • Rapid identification and assessment of study sites using our established relationships with clinical research sites in Africa
  • Customized questionnaires to meet your requirements
  • On-site assessments via a thorough checklist
Site development & managment
Our site selection and assessment services include:
  • Identification of personnel who can be deployed from health response teams
  • Full-time site support to assist research-naïve site staff
  • Pre-deployment training for roles, study procedures and processes
  • When possible, web-based re-training as issues arise
  • Therapeutic and protocol-specific training for each study by in-house subject matter experts
  • ICH GCP and protocol-specific training tailored to the sites’ needs
  • Informed consent training
Project managment
Our project management services include:
  • Pre-deployment training for roles, study procedures and processes
  • Site development plans based on prior site assessments
  • Mentoring to build the capacity of site staff
  • Clinical operations support
  • Definition of study risks and identification of critical risk indicators, in collaboration with the sponsor
  • Documentation of timelines and deliverables
  • Implementation of financial platforms for strict financial scrutiny and to serve diverse systems and local requirement
  • Clinical monitoring
    Our clinical monitoring services include:
  • Development of a study-specific monitoring plan in collaboration with the sponsor
  • Customizing a recruitment and retention plan for each site
  • Therapeutic and protocol-specific training for each study with continuous support by in-house subject matter experts
  • Highly skilled field activities including assessment, initiation, interim monitoring and closeout visits
  • Site management via a combination of on-site and remote monitoring to minimize risk and ensure compliance with ICH-GCP guidelines
  • Regulatory support
    Our regulatory services include:
  • Registration of a study’s progress in clinicaltrials.gov
  • Quality oversight and regulatory operations management
  • Site support to meet local and central ethics/IRB requirements
  • Support for regulatory strategy and operations
  • Review of study product labeling, drug shipment authorization, protocol, trial master files and other essential documents