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ViSU is a Cloud based Centralized Regulatory Information Management (RIM) solution to efficiently manage your regulatory data, activities, processes, submissions and commitments.
mEDC is a web based electronic data capture system that offers faster study setup, flexible configuration, detailed reporting, improved query management, all leading to enhanced user experience.
A single centralized system across the study/project portfolio will enable companies to have a single source of truth to utilize for systematic monitoring of portfolio, project and studies performance, risk and compliance policies across.
LABELai is a patent-pending tool that enables companies achieve their End-to-End labeling goals. With option of using the system for either Content Management or Label Operations or both, companies can pick the part of the tool that enhances their productivity and compliance.
In an era of improved Regulations to guarantee patient safety, Clinical Supply chain managers don't need to be warned of the things that can go wrong in their efforts to deliver supplies to many remote sites Globally in a Clinical Trial. DDi has 2 versions of IRT systems for Clinical Supplies. Both are Modular and Parameter based systems where each module is plug and play.
Vistaar is a Regulatory Intelligence and Compliance platform. For over 8 years, we are helping companies get up-to-date global Requirements, Guidance, and Regulations. Verify Applicability & perform Cross- functionality Assessment (with built-in task & workflow management). Get compliance overview at all times by country, regulation and functions. an All within single platform. Vistaar is a DDi product.
DDismart Reviews
Verified User in Information Technology and Services
Manage your clinical data with efficiency
MD DILSHAD A.
Student at Rajiv Gandhi Prodyogiki VishwavidyalayaViSU a centralized RIM
About
What is DDismart?
DDi is a regulatory, quality, and clinical technology platform built exclusively for Pharma, Biotech, Medical Device/IVD, and Consumer Health companies, combining AI-driven automation with expert human review. DDi replaces fragmented spreadsheets and siloed tools with a single system spanning regulatory intelligence, RIM (products, registrations, submissions), eCTD and regulatory submission publishing, labeling/CMC and technical regulatory writing, UDI/EUDAMED/EU MDR/IVDR compliance, eIFU management, and clinical supply (IRT/RTSM). DDi serves life sciences companies of all sizes — from emerging biotechs to global top-100 firms — helping regulatory and clinical teams move faster without sacrificing the accuracy a health authority audit demands.