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mClinical Products
With extensive experience in providing full clinical services, DDi leverages its domain, functional and technical expertise in developing some of the dynamic and innovative e-clinical solutions for the Life Sciences industry.
In today’s challenging environment, our mClinical product portfolio serves the technology needs during the drug development and clinical trial phases— from Phase I through regulatory submission, post-approval trials and pharmacovigilance. Our products are comlpetely validated and have been designed to support the requirements of internationally recognised ICH- GCP, FDA 21 CFR Part 11 and other regulatory standards.
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mClinical Product Suite |
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A web-based Electronic Data Capture tool for managing single or multi-site clinical research studies with complete audit trail. mEDC is a comprehensive, yet highly configurable electronic data capture application.
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A web-based automated coding system that supports multiple dictionaries minimizing the manual efforts required to code verbatim terms.
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A simple and robust web-based application for centralized patient randomization. It supports open label, single blind and double blind randomizations in multi-arm studies.
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A web-based Electronic Document Management system designed for global life sciences organizations to manage all clinical, IRB/EC, regulatory, SOPs, QMS documents directed by regulatory authorities including FDA, EMEA, PMDA and others.
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A thin client web based technology taking the most advanced features of internet, including xml support to facilitate the sharing of information and documents in a workflow environment.
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A secured web-based solution that helps site members, trail managers, monitors, clinicians and other clinical team members to communicate, collaborate and contribute effectively on a single and simple medium.
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