• +260 211 242 257/58/59
  • croservices@cidrz.org
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Our Services

We can partner with you to fully manage your clinical trial from beginning to end or we can tailor a suite of services to meet your specific trial needs.

Regulatory affairs

  • Perform local and international ethics and regulatory submissions according to national requirements.

Project management

  • Manage all activities necessary to maintain the project within timelines, quality and budget.

Site Operations management

  • Manage all site operational activities.

Clinical Monitoring

  • Conduct monitoring visit to ensure quality.

Institutional Biosafety Committee (IBC) Services

  • Oversee and evaluate research undertaking rDNA activities.

Site preparation for inspections and audits

  • Provide support to sites for study start up, inspections and audits.

Archiving Services

  • Management and storage of Data.

Translations

  • Translation of documents in local languages.