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

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.
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.
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.
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.
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.
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.
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.
KaMma Clinical Research
📧 Email: info@kammaclinicalresearch.com
Let’s build a healthier future together.