Accelerate Ethical Clinical Trials Across Africa

Ka Mma Clinical Research delivers community-trusted, regulator-ready trial operations with quality, speed, and participant safety at the center.

Built for Trust & Impact

Ka Mma Clinical Research supports sponsors, CROs, and investigators with reliable trial delivery grounded in patient dignity and scientific rigor. We combine local site knowledge, disciplined operations, and quality-first documentation to help studies move from start-up to close-out with fewer delays. Our team prioritizes clear communication, ethical conduct, and practical problem-solving—so communities are respected and data are dependable.

Trial Delivery You Can Trust

Site Feasibility & Start-Up

Pragmatic feasibility, site readiness checks, document collection, and activation tracking to reduce cycle time. Ideal for sponsors and CROs needing clear visibility, predictable milestones, and fewer startup bottlenecks.

Clinical Operations Management

Day-to-day coordination from first patient in to close-out—visit planning, vendor coordination, issue escalation, and progress reporting. Built to keep teams aligned, participants supported, and timelines intact.

Quality & Regulatory Support

GCP-aligned documentation, QC checks, CAPA support, and audit readiness for ISF/TMF. Designed to strengthen compliance, reduce findings, and ensure data credibility from the start.

Take a look

KaMma Clinical Research: Where Compassion Meets Science

01

Prioritize Participant Experience

Design visit flow that reduces burden: clear consent language, culturally appropriate materials, reminder calls/SMS, and respectful privacy practices. Track wait times and missed visits to continuously improve retention while protecting dignity and autonomy.

02

Strengthen Data Quality Early

Prevent deviations by standardizing source documentation, training staff on protocol-critical data, and using simple checklists at each visit. Early risk reviews and query trend tracking reduce rework and keep timelines predictable.

03

Align Stakeholders From Day One

Set expectations with a startup playbook: roles, escalation paths, recruitment targets, and reporting cadence. Short weekly updates with action owners help sponsors, sites, and vendors stay aligned and avoid late-stage surprises.

Clinical Research Services in Africa: End-to-End Trial Management & Operations

Site Start-Up That Moves

Accelerate activation through readiness assessments, essential document collection, and proactive IRB/EC coordination. A clear startup tracker and templated packages reduce back-and-forth and keep milestones visible to all stakeholders.

Recruitment With Local Insight

Build recruitment plans that reflect real referral pathways and community dynamics. Use pre-screen tools, outreach scripts, and feasibility-driven targets; monitor screen-fail reasons weekly and adjust messaging and criteria clarification fast.

Monitoring & Close-Out Readiness

Keep TMF/ISF audit-ready with routine QC, documented CAPA, and timely query resolution. Close-out is smoother when IP accountability, archiving plans, and reconciliation tasks are embedded throughout delivery—not left to the end.

Our Approach & Therapeutic Focus: Community-Centered, Ethical, Technology-Enabled Trials

Ethics-First Trial Conduct

We operationalize GCP with practical safeguards: consent comprehension checks, AE/SAE reporting discipline, and privacy-by-design handling of participant information. Decisions are documented, traceable, and respectful of local context.

Technology That Reduces Friction

Use fit-for-purpose tools—EDC hygiene, ePRO where appropriate, and simple dashboards for enrollment and deviations. The goal is fewer manual errors, faster visibility, and smoother collaboration between sponsor, CRO, and site teams.

Therapeutic Areas, Built Responsibly

We support studies that benefit communities, with careful attention to feasibility, referral networks, and follow-up practicality. Our focus is delivering reliable endpoints while ensuring participants understand the study and feel supported throughout.

Trusted by Sponsors & Sites

Contact US

KaMma Clinical Research

 📧 Email: info@kammaclinicalresearch.com 

Let’s build a healthier future together.