Regulatory & IRB Approvals
We help our clients obtain the necessary regulatory permissions and ethical clearances for conducting research involving human subjects prior to study start-up.
Training
Clinical Research Training equips individuals with the knowledge and skills needed to effectively and ethically carry out clinical research and contribute to the advancement of medical knowledge.
Study Start-Up Activities
We handle all the administrative and logistical preparations prior to study commencement to ensure compliance with applicable regulations and guidelines.
IP Management
Effective IP management is essential for maintaining the integrity of the trial, ensuring participant safety, and complying with regulatory requirements.
Study Initiation
Study Initiation refers to when a clinical trial is officially launched and all the necessary components are put in place to ensure its successful execution.
Patient Recruitment, Engagement & Retention
We are experienced in identifying and enrolling eligible participants, maintaining their active involvement throughout the study, and minimizing participant dropout.
Study Monitoring
At AFRICRO, we perform ongoing oversight and evaluation of a study to ensure that it is conducted according to the protocol, applicable regulations, and Good Clinical Practice (GCP) guidelines to protect the rights and welfare of study participants and to ensure the integrity of the data collected.
Safety Monitoring & Reporting
We perform the systematic and ongoing assessment of participant safety throughout the duration of a clinical trial in order to identify, evaluate, and manage any adverse events or safety concerns that may arise during the study.
Data Capture, Management & Analysis
Data capture, management, and analysis play a crucial role in clinical research to ensure the collection, organization, and analysis of high-quality data. These processes contribute to the generation of reliable and meaningful results.
Biostatistics
We provide the statistical expertise necessary for study design, data collection, analysis, interpretation, and reporting.
Study Reporting
At AFRICRO, we comprehensively communicate study findings and results to disseminate research outcomes, contribute to the scientific knowledge base, and facilitate evidence-based decision-making in healthcare.
Data Archival
We are experienced in the systematic organization, indexing, and long-term preservation of research data, ensuring its integrity, accessibility, and traceability for future reference and regulatory compliance.
Biospecimen Collection
Biospecimens, such as blood, urine, tissue samples, and other biological materials, provide valuable information about disease biomarkers, genetic factors and treatment responses.
Patient Interviews, Questionnaires & Surveys
Patient interviews and surveys are valuable approaches that provide insights into patients’ experiences, perceptions, and outcomes related to a specific disease, treatment, or intervention.
Study Management
From project planning & timeline development to study team formation, we manage the overall coordination, oversight and execution of a clinical trial from start to finish.
Flexible,
Customised Service
These services are designed to provide flexibility in terms of features, options, and delivery methods, allowing researchers or sponsors to select and customize the services according to their unique requirements and study objectives. We combine our passion for scientific research, knowledge of the African terrain and world-class experience to implement studies quickly and efficiently, without compromising on patient safety or data quality.
