Sites

Enrolment application

Sites

You are welcome to be part of this key role of competent and reliable asset if you are not already. Sites are major key players in clinical trials as they provide the location, structures, equipment and materials, and all professionals that are needed for a successful clinical trial successfully process. Our sites include health centres, hospitals, and research institutes.

benefits of clinical trials

Access to research funding

As a site, we will have access to resources through the period of trials. Allocation of funds is usually granted per project as it is vital in ensuring sustainability of the trials.

Training and development

Staff are trained and exposed to studies and practices that enhance their competences and development through the research period. Gaining of adequate knowledge, attaining practical skills and developing the right attitude are imperative and are acquired for clinical trials.

Collation and harnessing clinical data

Our sites are responsible for study documents and record protection and retention as well as efficient data management. This can be used subsequently in implementing hospital documentation planning.

Exposure to global clinical conduct

Through our experiences and network relationships, our sponsors and partners are global, hence, exposing every staff on international conducts such as ICH, GLP, SOP, GCP among others’

Is your site positioned to partner with us? Fill out the form below and let us reach out to you!
Name(Required)
Address(Required)

Staff Qualification

(Please note not all site staff has to have experience, at least the investigator should have conducted other studies as a sub-investigator).
(protocol, CRF, lab manuals etc.)

Facilities and Equipment and Calibration records

Documentation Procedures

Patient Population

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