Operational resilience
Facilities are planned around uptime, utilities, staffing realities and dependable isotope supply.
We plan, equip and operationalize cyclotron and radiopharmaceutical facilities for real-world African conditions — resilient, compliant and ready for clinical impact.
The delivery model is intentionally streamlined: make the facility resilient, make compliance practical and make the operating team self-sufficient.
Facilities are planned around uptime, utilities, staffing realities and dependable isotope supply.
Quality systems, documentation and validation are built into the project rather than added later.
Recruitment, training and SOPs help teams operate confidently after commissioning and handover.
From cyclotron operations to GMP quality control, radiopharmacy, PET-CT and SPECT-CT imaging and theranostics delivery, each workstream is coordinated as one practical delivery system.
Cleanroom design, shielding, equipment specification, procurement and construction oversight.
Cyclotron setup, isotope production optimization, reliability planning and contingency preparation.
Synthesis modules and robust production workflows for FDG and advanced radiotracers such as PSMA.
Radiopharmacy hot lab delivery — lead-shielded hot cells with leaded-glass laminar airflow hoods, kit-based radiotracer preparation, dose calibration and dispensing workflows for daily clinical supply.
QC laboratory establishment and validated analytical methods across HPLC, GC, MCA, TLC and supporting instrumentation.
End-to-end PET-CT suite planning — from scanner room design and shielding to oncology imaging workflows that bring cancer detection to the clinic.
SPECT-CT suite delivery — gamma camera rooms, radiotracer imaging protocols and whole-body scintigraphy for bone, cardiac and oncology studies.
Theranostics capability and delivery — pairing diagnostic imaging agents with therapeutic isotopes so the same molecular target can be seen, staged and treated.
A clear sequence keeps stakeholders aligned while the facility moves from planning through commissioning and clinical readiness.
Define the clinical, operational and regulatory brief.
Plan workflow, cleanrooms, shielding and utilities.
Specify and source equipment against performance requirements.
Oversee installation, qualification and validation.
Train people, document SOPs and transition into production.
Led by Founder & Managing Director Dr. George Afari, delivery spans operations, tracer development, manufacturing, quality systems and workforce development.
Share your site, timeline and clinical objective. We will help shape the practical route to production.
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