Pioneering Excellence in Africa with AfriLeadTech
Our Services
We provide comprehensive and end-to-end support to pharmaceutical,biotechnology, and medical device companies throughout the entire lifecycle of clinical trials. We cover all activities and support functions required from planning, executing, and managing clinical trials.
Project Management
Strategic planning and oversight of trial set-up and conduct, ensuring adherence to Good Clinical Practice (GCP) guidelines and regulatory requirements while delivering projects within timelines and budgets.
Site Selection and study set-up
Identifying and qualifying suitable investigational sites and managing relationships with these sites throughout the study.
Regulatory Affairs & IRB/IEC Authorizations
Obtaining all necessary regulatory & Ethical approvals from relevant health authorities, ethics committees and other relevant local bodies.
Site Management and Monitoring
We provide on-site and remote monitoring resources to ensure data integrity, ethical conduct and compliance with study protocols and regulations.
Data Management & Document Management
Collection, validation, and management of study data and documents using electronic systems.
Patient Recruitment and Retention
Strategies to identify and retain suitable study participants.
Medical Writing
Protocol writing, clinical study reports, and other essential study documents.
Pharmacovigilance and Safety Monitoring
Development of safety management plans and coordination with safety and medical monitoring vendors. Provide Post-Marketing Surveillance
Vendor coordination services
Sourcing local vendors and Coordination of all vendors required for the delivery of clinical trials data testing and sample analysis. 
CONTACT US
Free consultation with us now
For comprehensive details regarding the
execution of clinical trials in various
African countries, please don’t hesitate
to contact us at info@afrileadtech.co.za.
We are here to assist you with valuable
insights and guidance.