AI-Powered Innovation in
Drug Development
At C-Search Clinical Trials LTD, we harness the power of Artificial Intelligence (AI) to revolutionize the drug development process, ensuring faster, more efficient results.
From drug discovery to patient recruitment for clinical trials, our AI solutions streamline and optimize each step, providing pharmaceutical companies with unmatched insights and precision. We are the leading experts in AI-driven tools that transform how companies develop and test life-saving treatments.
Contact us today for personalized guidance on integrating AI tools to enhance your drug development processes and accelerate clinical trials.
About C-search
C-Search Clinical Trials LTD, established in 2016 by Sima Reuven, who has been working in the field since 2000.
C-Search is a registered enterprise in Israel specializing in providing regulatory consultancy services to pharmaceutical and biotechnology companies worldwide.
As an overseas representative, our company is crucial in assisting international firms with navigating the intricate local regulations in Israel.
We guide companies through the complex landscape of regulatory compliance.
our services
C-Search specializes in the start-up phase of clinical trials in Israel,
offering tailored services for a successful trial initiation.
Thorough feasibility studies and site evaluation: In-depth assessments of patient demographics, site capabilities, and enrollment potential using sophisticated AI tools.
Essential Documents Development and regulatory submissions: Creating compliant documentation, including the Informed Consent Form, adhering to Israeli standards, and regulatory submissions to local Ethics Committees and the Ministry of Health.
Budget and Contract Negotiations: Transparent financial negotiations with local trial sites and legal authorities.
In-house and outsourcing Senior CRAs.
Efficiency Comparison
Streamlined Start-Up Phase in C-Search Clinical Trials Ltd vs. Large CROs
Our comparison underscores the efficiency of C-Search in the start-up phase of clinical trials. It typically achieves timelines that are approximately half of those of larger CROs.
Why C-Search?
Complementing large CROs, we provide two collaboration models:
- Directly collaborate with your CRO for integrated and efficient start-up
- Manage all start-up activities before transitioning the project to your CRO.
Our effective communication guarantees a streamlined and successful project, regardless of the collaboration method.
Expertise and Focus
Our precision in regulatory matters ensures efficiency in all processes.
Customization and Flexibility
We offer the advantage of tailored solutions that are not limited by standardized processes and cater specifically to your unique needs.
Cost Efficiency
Direct engagement with our specialized team often proves more cost-effective than working with larger, less specialized organizations.
Speed and Ability
Our team can swiftly navigate complex regulatory landscapes, ensuring your project timelines are effectively and efficiently met.
Focused Relationships
We prioritize close collaboration and clear communication, fostering smoother processes and successful outcomes.
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