CLINICAL RESEARCH ORGANIZATION
RAMBAC is a full-cycle contract research organization supporting clinical trials in Uzbekistan — from protocol development to final regulatory submission.
ABOUT US
RAMBAC is a contract research organization with deep expertise in the Uzbekistan clinical research market.
We provide end-to-end support for pharmaceutical and biotechnology companies — from study design and regulatory submissions to site management and final reporting.
Our team brings direct access to leading investigational sites and Principal Investigators across the country, enabling fast and compliant trial start-up.
AREAS OF THERAPEUTIC EXPERTISE
Our services now explicitly include Phase I studies in oncology patients — with specific competencies in Dose Escalation design and complex oncology protocol management, ensuring rigorous safety oversight at every stage.
OUR SERVICES
RAMBAC provides end-to-end support for Phase I–IV clinical trials in Uzbekistan.
Assessment of study feasibility, patient population, site capabilities, and principal investigator availability.
Dossier submission and approvals from the Ministry of Health and Ethics Committees; regulatory communication.
Protocol preparation and translation, Investigator's Brochure, informed consent forms, and site contracts.
On-site and remote monitoring per ICH-GCP; data quality control and source data verification.
Coordination of all study stages, budget and timeline control, and sponsor reporting.
CRF/eCRF development, EDC setup, data validation and database lock.
SAP development, data analysis, and statistical reports.
Protocols, CSR, publications, and regulatory summaries.
SAE/SUSAR collection, assessment and reporting; PV-system support.
Import, storage, distribution and accountability per GDP/GMP.
Site and investigator identification and qualification; GCP training.
Independent audits of sites, systems and documentation; regulatory inspection support.
Study design, local regulatory requirements, and drug registration advice.
OUR ADVANTAGES
Deep expertise in Uzbekistan's clinical research landscape, regulatory environment, and healthcare system.
Efficient coordination with sites, investigators, ethics committees, and regulatory authorities.
Clinical trial operations aligned with GCP and ICH standards.
Specialists in monitoring, project management, regulatory affairs, data management, quality assurance, and medical writing.
A personalized approach shaped around the sponsor's goals, study design, and operational needs.
Established relationships with leading clinical centers and experienced principal investigators.
Integrated support from feasibility and regulatory submission to monitoring, data management, and final reporting.
GET IN TOUCH
CONTACT US
Rambac LLC
Tashkent, Mirzo-Ulugbek district,
Lashkarbegi MFY, Niyozbek yo'li street,
30, office 204A
