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Edmonton, T6T1V4, Canada
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Contract Research Organization

Contract Research Organization

Conduct Research can work as your CRO, and help with the effective planning, execution, and management of the trials. Tracking the progress, and supervising changes in the study, and effective database management are important clinical trial processes that must be accomplished carefully. Conduct Research has expertise in all these areas.

It is important to note that clinical compliance with regulatory agency guidelines is crucial, and adhering to Good Clinical Practice (GCP) standards is part of our role as it acts as the trial’s central hub, connecting the sponsor with other stakeholders such as regulatory agencies, ethics committees, vendors, hospitals, etc.

Conduct Research can handle several types of research projects. From literature reviews to first-in-human trials, and to phase escalation of biopharmaceutical and device clinical research projects, we have the expertise to meet your requirements. We leverage our expert leadership to design and implement your research and can efficiently inform clinical decisions and practices.

Functional Capabilities

Some of our major service areas as a CRO are:

Project Management
Study planning and oversight
Clinical Monitoring
Medical and Safety Monitoring
Safety Monitoring Boards
Regulatory Affairs
Database Creation and Management (TMF)
Case Report Forms (CRFs)
SOPs and Working Practice Development