Governance and qualification
Four standing bodies with defined decision rights, and formal qualification of cancer centers and investigators against one standard, reviewed annually.
Center of Excellence ยท Oncology
A collaborative network of leading cancer centers, investigators, and research institutions supporting Phase I to IV oncology clinical trials, under one quality system and one point of accountability.

The Oncology Center of Excellence
Africa's cancer burden is rising faster than the research infrastructure needed to address it. Capability exists, but it is fragmented, unevenly documented, and difficult for a global sponsor to access at scale. The Center resolves that fragmentation.
Qualified cancer centers, investigators, and laboratories across the continent.
ICH GCP-aligned quality management with central oversight and inspection readiness.
A single commercial and operational relationship from feasibility to close-out.
Why Oncology
Cancer is one of Africa's fastest-growing health challenges, with more than 1.18 million new cases and over 760,000 deaths each year. The continent is projected to see one of the largest increases in cancer incidence worldwide by 2050.
Yet African patients remain substantially under-represented in oncology research. That gap limits the evidence base for populations carrying a rising share of the global burden, and delays access to innovative therapies. The Center addresses both problems at once.
1 Source: GLOBOCAN / IARC. Confirm edition and year before publication.
Therapeutic Focus Areas
Focus areas are reviewed annually by the Oncology Scientific Advisory Group and reflect demonstrable network capability.
Clinical Research Capabilities
The Oncology Research Network
The Center brings together a growing network of carefully qualified oncology institutions, investigators, and laboratories across Africa. Centralized governance, standardized quality systems, and coordinated operational support enable sponsors to run efficient, high-quality trials across multiple countries.
Participation is earned, not permanent. Organizations are admitted through formal qualification and reviewed annually against performance and quality standards.
Network composition is held as a confidential commercial asset. Individual institutions may be identified to a sponsor under confidentiality during feasibility.
What GLS Provides
Coordination is the outcome, not the service. GLS operates the oncology network as a working platform.
Four standing bodies with defined decision rights, and formal qualification of cancer centers and investigators against one standard, reviewed annually.
A single ICH GCP-aligned quality system: SOPs, training, deviations and CAPA, audit, and continuous inspection readiness.
One protocol interpretation, one set of SOPs, one training standard, and one data model across countries and institutions.
Centralized oncology feasibility, one master contract, and budgets negotiated once rather than country by country.
Country-by-country submissions coordinated centrally, with designated medical monitoring and defined safety escalation.
Molecular pathology, genomics, and biobanking coordinated with the protocol; data integrity and privacy standards; and investigator development.
Governance and Quality
Every institution and investigator operates under a common governance framework. Sites are qualified before admission, monitored during delivery, and reviewed annually. Quality management is centralized rather than delegated, so standards do not vary by country or site.
Ultimate decision authority. Owns strategy, risk appetite, network expansion, and escalations.
QuarterlyIndependent scientific counsel: therapeutic strategy, focus areas, feasibility standards, and scientific integrity.
QuarterlyOperational delivery: site qualification decisions, feasibility, and performance management.
MonthlyQuality system ownership, audit program, deviations and CAPA, and inspection readiness.
MonthlyInstitutions and investigators apply through the qualification process.
Structured assessment of expertise, trial history, compliance, and infrastructure.
Site qualification visit, SOP and pharmacy review, and data-integrity check.
Contracting, onboarding, and training completion.
Performance and compliance review, with remediation, suspension, or withdrawal where standards are not met.
Why Sponsors Partner with GLS
One commercial and operational relationship gives sponsors coordinated access to the whole network. Site identification, feasibility, regulatory coordination, quality oversight, contracting, and execution all run through a single partner.
Qualified cancer centers, investigators, and laboratories across the continent.
ICH GCP-aligned quality management with central oversight and inspection readiness.
A single commercial and operational relationship from feasibility to close-out.
Become Part of the Network
The Center expands through partnership with qualified oncology institutions, investigators, laboratories, academic medical centers, and industry collaborators. Interested organizations are invited to enter the GLS qualification process.
Whether you are developing oncology therapeutics, biologics, cell and gene therapies, diagnostics, or medical devices, the Center provides a governed, collaborative platform to accelerate clinical development across Africa.