Our expertise
CERC provides end-to-end management of clinical trials or targeted support for specific project phases.
From study design to clinical report production, our teams ensure operational excellence, scientific rigor, and full regulatory compliance at every step of the process.
Our integrated structure allows us to manage the full life cycle of a clinical trial, including study design, investigator and site selection, study documentation, monitoring, data analysis, and reporting.
Who we support
Organizations seeking a trusted partner to run their clinical studies globally or regionally, with scalable support ranging from full-service management to selected operational tasks.
CERC supports industry sponsors, academic institutions, and investigators with tailor-made project models adapted to each study’s needs.
Engagement options
- Full-service management: complete oversight from planning to publication.
- Modular collaboration: CERC manages one or more aspects such as monitoring, data management, or reporting.
- Study rescue and audit: intervention at any project stage to optimize timelines and data quality.
What we deliver
- Study planning and protocol development
- Investigator and site selection leveraging CERC’s global network
- Study documentation and monitoring in compliance with GCP and ISO 14155
- Data management and statistical analysis
- Central imaging and core laboratory coordination
- Safety management and regulatory alignment
- Clinical study reports and publication support
Our process
- Design: define objectives, endpoints, and study design aligned with regulatory expectations.
- Activate: select and train investigators, initiate sites, and oversee enrolment.
- Monitor: ensure protocol adherence and data integrity through centralized and on-site monitoring.
- Analyze: manage data cleaning, validation, and statistical analysis.
- Report: deliver high-quality reports and ensure dissemination through publication support.
Why CERC?
- Proven track record across all trial phases from post-market registries to double-blind randomized studies.
- Multilingual and multicultural team speaking over 20 languages, enabling smooth communication in multinational trials.
- Global reach through CERC Asia and US partnerships for worldwide project execution.
- Strong operational culture built on transparency, quality, and responsiveness to sponsor needs.
Typical deliverables
Project plan, protocol and Case Report Forms (CRF) package, monitoring plan, data management plan, safety management report, study progress reports, final Clinical investigation reports (CIRs), and publication summary.
Sample outcomes
- Accelerated patient enrolment through optimized site engagement.
- Improved data integrity and reduced query rates via proactive risk-based monitoring.
- Seamless collaboration with sponsors and CRO partners through flexible governance models.
From planning to publication, CERC ensures your study runs smoothly and efficiently.
Contact us to discuss how we can support your next clinical trial.
