Clinical Trial Services
At Curaclin Research, we specialize in end-to-end Clinical Trials Management to help sponsors and CROs bring innovative treatments to market efficiently and ethically. Our services are designed to ensure seamless execution, compliance, and quality across all phases of clinical trials.
Our Clinical Trial Management Services
- Trial Planning and Design: Comprehensive trial design to meet specific objectives and regulatory requirements.
- Regulatory Submissions and Approvals: Ensuring compliance with local and global regulations for smooth approval processes.
- Site Management: Effective coordination and oversight of trial sites for optimal performance.
- Patient Recruitment and Retention: Strategies to recruit and retain participants, minimizing dropout rates.
- Data Management and Monitoring: Accurate data collection, monitoring, and analysis for high-quality outcomes.
- Safety and Risk Management: Proactive identification and mitigation of risks to ensure participant safety.
- Project Management: Expert management to ensure trials are completed on time and within budget.
- Close-Out and Reporting: Detailed close-out procedures and comprehensive reporting for regulatory submissions.
Why Choose Curaclin Research for Clinical Trial Management?
- Experienced Team: Our team comprises seasoned professionals with extensive expertise in clinical trial management, regulatory affairs, and therapeutic research.
- Customized Solutions: We tailor our services to the specific needs of each study, ensuring efficient execution and high-quality results.
- Global Reach: With a network of trial sites and investigators worldwide, we manage trials across diverse geographic regions and patient populations.
- Focus on Quality and Compliance: We adhere strictly to ICH-GCP guidelines, regulatory standards, and ethical principles, ensuring the highest levels of compliance.
- Technology-Driven Processes: Utilizing state-of-the-art tools and platforms, we enhance data accuracy, streamline processes, and improve decision-making.
At Curaclin Research, we are committed to helping sponsors and CROs achieve clinical trial success by delivering innovative solutions, operational excellence, and unwavering focus on patient safety. Whether you're planning a Phase I trial or preparing for market approval, our expertise ensures every aspect of your trial is managed with precision and care.
Contact us today to discover how Curaclin Research can advance your clinical research goals.
Choosing a definite site allows to avoid problems that will impede the progress of a trial. Curaclin Research has varied and vast know-how of therapeutic areas and regional sites across India which are managed by specific local site-heads and teams.
Trained staff possess expertise in the submission, monitoring, and approval processes related to both national and international standards and regulations. At Curaclin Research, we recognize that the success of any clinical trial begins with effective site selection and a smooth trial start-up process. Our comprehensive services ensure that the right sites are chosen and trials are initiated efficiently, enabling sponsors to achieve their goals within timelines and regulatory requirements.
Curaclin Research takes pride in having a well-structured Pan india Network of trained CRCs with experience in ICH GCP R2 consultancy work who can carry out various tasks across India. All professionals possess a competent command of the English and Regional Language. Different monitoring strategies are implemented, which are a combination of both study monitoring visits and remote monitoring as well as features that are embedded in the specific study design. A risk-based adaptive approach to the monitoring of study management activities is applied in order to provide effective supervision at optimal costs.
It is also ensured that the communication of all relevant issues is handled effectively with respect to detail and time, due to the fact that there are detailed procedures in place and a communication plan for each study. Protocol violations are followed through further by a combination of our EDC and Study portal systems which enable this crucial study activity to be managed electronically, real-time and with no paper. In the same way, the electronic solution is a major element for the success of questions being raised and answered within the timeframes set for data base lock and data base freeze.
A CuraclinResearch expert team provides assistance targeting regulatory issues concerning clinical phase study (I-IV Including observational & BA/BE Studies) and the registration of a medical device and nutraceutical products. The staff has the necessary regulatory support across the regions within which local and international regulations and guidelines are included.
These regulatory services include:
a. Assessing the completeness and correctness of the regulatory submission documents
b. The submission package is prepared
c. Maintenance of electronic submissions in line with the applicable requirements
d. Maintenance and support of ClinicalTrial.gov and EudraCT
e. Finalization of regulatory approvals
Curaclin Research is equipped with a comprehensive range of advanced instruments, ensuring the highest standards in research and clinical diagnostics.
Our offerings include-
1. Ultra Low Deep Freezer (-86°C) – For long-term storage of biological samples at extremely low temperatures.
2. -20°C Deep Freezers – Ideal for storing reagents and samples at moderate sub-zero temperatures.
3. Refrigerated & Normal Centrifuge – Essential for sample separation and processing.
4. Laminar Airflow – To maintain a sterile working environment for sensitive procedures.
5. 2 to 8°C Scientific Refrigerator – For precise temperature control to store temperature-sensitive materials.
6. Infusion Pump – Accurate and reliable device for the continuous infusion of fluids.
7. BOB Incubator – For controlled incubation of biological samples.
8. Multipara Instrument for Continuous Vitals Monitoring – Real-time monitoring of multiple vital signs in clinical settings.
9. Vascular Doppler – A diagnostic tool for measuring blood flow and detecting vascular conditions.
10. Data Logger (Up to -80°C) – To monitor and record temperature data for ultra-low storage environments.