Why C-Search?
At C-Search Clinical Trials Ltd., we provide senior-level clinical research support tailored to the needs of global pharmaceutical, biotechnology, and medical device companies conducting clinical trials in Israel.
Our strength lies in combining regulatory expertise, clinical operations, and quality management within a single experienced team, enabling sponsors to work with a single trusted local partner throughout the study lifecycle.
Why sponsors choose C-Search
- More than 25 years of clinical research experience.
- Comprehensive Regulatory Affairs and Clinical Trial Start-Up services in Israel.
- Senior CRA Monitoring Services, including Site Qualification, Site Initiation, Interim Monitoring, Remote Monitoring, and Close-Out Visits.
- Experience across Phase I-IV clinical trials and a broad range of therapeutic areas, including oncology, neurology, rare diseases, pediatrics, ophthalmology, dermatology, rheumatology, endocrinology, respiratory diseases, infectious diseases, and medical devices.
- Strong working relationships with leading Israeli medical centers and investigators.
- Flexible, senior-level support with direct communication and rapid response.
- A documented Quality Management System (QMS) developed in alignment with the principles of ICH-GCP and ISO 9001, ensuring consistent, inspection-ready, and quality-driven processes.
- Proven experience supporting international sponsors, CROs, and emerging biotechnology companies.
- Access to a long-standing professional network of independent boutique CROs and senior clinical research professionals across selected countries in Western and Eastern Europe.
Our commitment is to deliver high-quality, reliable, and efficient clinical trial services while maintaining the highest standards of regulatory compliance, scientific integrity, and operational excellence.
Whether you require regulatory support, study start-up, clinical monitoring, or quality-focused project support, C-Search provides the expertise and local knowledge needed to successfully conduct clinical trials in Israel.
Our team swiftly navigates complex regulatory landscapes to ensure your project timelines are met with efficiency and precision
We offer the advantage of tailored solutions that are not limited by standardized processes and cater specifically to your unique needs
We prioritize close collaboration and clear communication, fostering smoother processes and successful outcomes
Direct engagement with our specialized team often proves more cost-effective than working with larger, less specialized organizations
Local Expertise Across Israel and Europe
Sponsors planning multinational studies can work with C-Search for the Israeli scope while gaining access to trusted independent clinical research professionals in selected European countries.
Where appropriate, C-Search can coordinate a combined operational proposal and help align the participating teams, responsibilities, timelines, and communication, while preserving the local expertise required in each country.
Real-World Data Collaboration
Through our collaboration with IOMED, a leading data-space platform that structures and standardizes real-world healthcare data using the OMOP Common Data Model, C-Search helps sponsors, CROs, and hospitals generate real-world evidence and improve the time-to-market and precision of clinical trials.
Learn more at iomed.health.
Clinical Trial Oversight Technology
Through its collaboration with Mayet Solutions Ltd., C-Search connects sponsors and CROs with purpose-built technology designed to strengthen clinical trial oversight, traceability, and inspection readiness.
Mayet Solutions
Mayet builds software for the people who run clinical trials. The company was founded in 2023 by Tom Lazenby, following more than a decade in clinical research and clinical quality assurance. Mayet's solutions are designed to replace fragmented spreadsheets and manual oversight processes with structured, traceable systems developed specifically for regulated clinical development.
Visit MayetVendorVigilance
VendorVigilance provides sponsors and CROs with systematic oversight of the vendors supporting their clinical programs, covering vendor selection, qualification, risk, performance, contracts, deliverables, and a continuous audit trail. The platform is designed to support the strengthened vendor-oversight and risk-management expectations of ICH E6(R3).
Explore VendorVigilanceTrialTrack
TrialTrack provides study-level control across studies, tasks, milestones, sites, vendors, and participants within a single clinical project-management platform. Its built-in audit trail and access controls support data traceability, GxP requirements, and inspection readiness without the cost and complexity of a traditional enterprise CTMS.
Explore TrialTrack