Proprietary ISO certificated clinical trial operation tools for efficient and accurate data collection & analysis
Clinical trials involve various technologies to facilitate research, data collection and analysis particularly in decentralized trials.
At VCLS, we have proprietary clinical trial tools and platforms such as CDMS, CTMS, ePRO, eTMF to facilitate the efficiency, accuracy, and safety of clinical trials, ultimately advancing the development of new treatments and therapies.
These solutions include:
- CTMS: Clinical Trial Management System
- CDMS: Clinical Data Management System
- eCRF: electronic Case Report Form
- ePRO: electronic Patient-Reported Outcomes
- eTMF: electronic Trial Master File
- IWRS: Interactive Web Response System
How can technological solutions be adapted to each clinical trial need?
What is the impact of clinical technologies on cost efficiency and data quality?
Streamlined Processes
Our integration of technology streamlines every aspect of the clinical trial process. From patient recruitment to data collection and analysis, our systems optimize efficiency, reducing trial duration and costs.
Data Security and Compliance
We prioritize the security of sensitive trial data. Our systems adhere to the highest data security standards, ensuring compliance with all regulatory requirements, and safeguarding participant privacy.
Customization
We understand that each clinical trial is unique. Our technology solutions are customizable to meet the specific needs of your research, ensuring a tailored approach for optimal results.
Cost-Efficiency
By harnessing the power of technology, we minimize overhead costs and resource allocation, making clinical trials more cost-effective without compromising quality.
Regulatory Expertise
Our team is well-versed in the ever-evolving regulatory landscape. We ensure that your trials not only meet but exceed all regulatory requirements, minimizing compliance-related risks.
Expertise 