Establishing dDgital Forms for Clinical Trial Data Collection that replace traditional paper-CRF.
Clinical Data Management System is a sophisticated software platform designed to collect, manage, and analyze clinical trial data.
A Clinical Data Management System (CDMS) is a sophisticated software platform designed to collect, manage, and analyze clinical trial data with precision and efficiency. It streamlines the entire data lifecycle from patient enrollment and data collection to analysis and reporting. By ensuring data accuracy, consistency, and compliance with regulatory standards, a CDMS enhances the quality and reliability of clinical research.
We are expertise in providing the various IT Services.
We are design and develop various clinical study related custom web application.
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We ECTS-LLP provides a wide range of activities and solutions for Information Technology (IT) services, delivered by technology specialists. These services often entail the administration, support, and deployment of many components of information technology inside a company.
eCRF (electronic Case Report Form) development focuses on establishing digital forms for clinical trial data collection that replace traditional paper-based techniques.
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eTMF (electronic Trial Master File) development entails building digital systems for organizing, managing, and storing clinical trial documents. It simplifies regulatory compliance.
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Developing an eSMF (electronic Site Master File) entails building digital systems for organizing, managing, and storing clinical trial documents. It simplifies regulatory compliance and guarantees easy access.
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Our SEO optimization service enhances online visibility, driving targeted traffic, and staying updated with SEO trends to help businesses achieve sustainable growth.
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IWRS (Interactive Web Response System) development entails establishing web-based systems to manage clinical trial activities such as randomization and drug supply tracking.
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Digital marketing services include a variety of methods and tools for increasing online presence, attracting potential clients, and driving conversions.
Learn MoreWe offer premium IT services that deliver cutting-edge solutions tailored to your business needs, including custom software development, robust cybersecurity, and seamless cloud integration. Our expert team ensures high performance, reliability, and innovation to drive your technology forward.
eCRFs can improve the accuracy and speed of data capture by using digital forms instead of manual entry.
Learn MoreResearchers can respond quickly to questions and anomalies, which can improve data quality and reduce administrative expenses.
Learn MoreeCRFs can allow for complex research project management by providing access to research background and monitoring every stage of the project.
Learn MoreThis eCRF facilitate with buld in audit trail for monitoring the entire activity on eCRF by the respective users, which is mandoatry by the regulatry.
Learn MoreIntroducing Enhanced Data Validation, the most recent feature of eCRF! This robust program automatically detects discrepancies and gives real-time feedback throughout data entering, ensuring data quality and integrity.
Our eCRF now includes robust electronic signature capabilities, transforming the way you handle and verify clinical trial documentation. With secure, compliant e-signature features, users can easily and efficiently sign forms and documents digitally, ensuring authenticity and regulatory adherence.
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We now provide flexible report generating with both soft and hard copy choices on our eCRF platform. For simple sharing and analysis, you may easily produce and export complete digital reports in a variety of formats, such as Excel and PDF.
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