DDi

DDi is a Prominent Partner to provide #Clinical Informatics and IT Solutions to the #LifeSciences Industry.

[DDi @DDiSmart]

🎉 Big News! DDi wins the “Best Global Regulatory & Clinical Development Partner 2025” award by GHP! 🌍🏆
Proud moment for our team and partners worldwide. Here’s to setting new standards in regulatory & clinical excellence! 💼💡

https://t.co/1VYWX0d9oi

#GHP2025 #GlobalHealth

[DDi @DDiSmart]

🚀 Still managing regulatory data in spreadsheets? DDi’s RIM solutions centralize submissions, compliance tracking & regulatory operations in one connected platform.
🔗 https://t.co/KS7kfnEMdP
#RIM #MedicalDevices

[DDi @DDiSmart]

🔍 Simplify global medical device registrations with MakroCare—country-specific dossiers, technical documentation & compliance-focused submission support for faster approvals.
🔗 https://t.co/8itjYhtYsX
#MedicalDevices #RegulatoryAffairs

[DDi @DDiSmart]

📘 Streamline electronic labeling with Visu eIFU by DDi compliant eIFU management, multilingual IFUs & audit-ready support for Medical Device and IVD companies.
🔗 https://t.co/LV99oHu5jI
#eIFU #MedicalDevices

[DDi @DDiSmart]

UDI compliance isn’t just regulatory—it’s operational risk.

DDi automates UDI validation + EUDAMED submissions to reduce errors and avoid costly rework.
🔗 https://t.co/R6vPGk7JM1
#UDICompliance #MedicalDevices

[DDi @DDiSmart]

RTSM / IRT Clinical Supply
Optimize clinical trials with DDi’s RTSM/IRT accurate randomization, better supply forecasting & faster study setup for efficient execution.

🔗 https://t.co/Y4bChnkPXs
#ClinicalTrials #IRT

[DDi @DDiSmart]

Regulatory Impact Assessment (RIA)
Stay ahead of regulatory changes with DDi’s RIA tool cut assessment time, reduce errors & gain a centralized view of global compliance.
🔗 https://t.co/anZgaB6AgC

#RegulatoryImpact #MedTech

[DDi @DDiSmart]

Regulatory Publishing Automation
Regulatory publishing is evolving with automation. Learn how agent-driven workflows reduce errors, improve QC & accelerate submissions.
🔗 https://t.co/yZgx4xktXm
#RegulatoryPublishing #Automation

[DDi @DDiSmart]

UDI Blog
Still think UDI is optional? It’s now key for traceability, recalls & compliance. Learn what it takes to get it right.
https://t.co/mbrA5a1RcE
#UDI #Compliance

[DDi @DDiSmart]

Medical Writing & Formatting Automation
Tired of fixing document formatting? DDi automates medical writing & formatting ensuring consistent, submission-ready outputs with less rework and faster timelines.
🔗 https://t.co/80pZ11c03x
#MedicalWriting #Automation

[DDi @DDiSmart]

RIMS Solution
Regulatory delays cost opportunities. DDi’s RIMS accelerates submissions, delivers real-time insights & simplifies global compliance with less manual effort.
🔗 https://t.co/KS7kfnEMdP

#RIMS #Compliance

[DDi @DDiSmart]

Visu eIFU
Medical device labeling is going digital. Visu eIFU by DDi enables secure, compliant electronic IFUs with version control and global MDR/FDA alignment.
Discover more: https://t.co/LV99oHu5jI

#eIFU #MedicalDevices

[DDi @DDiSmart]

EUDAMED UDI Lessons (Blog)
Avoid common EUDAMED UDI mistakes. This DDi blog shares key lessons from GUDID implementations, data pitfalls & governance insights for accurate submissions.
Read more: https://t.co/pzjsDu26Du
#EUDAMED #UDI

[DDi @DDiSmart]

Legacy Devices in EUDAMED (Blog)
Managing legacy devices under EU MDR? This DDi blog explains EUDAMED setup, obligations, exemptions & key compliance risks.
Read more: https://t.co/BlyrT7LQMe
#EUDAMED #MedicalDevices

[DDi @DDiSmart]

EUDAMED compliance under EU MDR requires structured data, accuracy, and ongoing updates.

DDi combines the EUDAMED software
Manage EUDAMED with confidence and clarity.
Learn more: https://t.co/LaV2LEaEk9

#DDi #EUDAMED #EUMDR #RegulatoryCompliance #UDI #DeviceRegistration

[DDi @DDiSmart]

UDI Compliance

Accurate UDI compliance supports device traceability & global approvals. DDi delivers end-to-end UDI governance, validation & GUDID/EUDAMED submissions with automation.

👉 https://t.co/R6vPGk7JM1
#UDICompliance #MedicalDevices

[DDi @DDiSmart]

Global UDI compliance starts with the right strategy. DDi helps define and execute UDI plans aligned with FDA, EU MDR, GUDID & EUDAMED requirements.
https://t.co/0jUNjF3jeK
#UDICompliance #MedicalDevices

[DDi @DDiSmart]

EUDAMED Compliance
EUDAMED compliance under EU MDR made simpler. DDi provides integrated software + consulting for Actor, Device & UDI data with audit-ready submissions.
👉 https://t.co/48eAzAgP5g
#EUDAMED #EUMDR

[DDi @DDiSmart]

Accurate UDI compliance is essential for traceability & patient safety. DDi offers end-to-end UDI management with automated GUDID & EUDAMED submissions across global markets.
🔗 https://t.co/ISp5rcQgKI

#UDI #MedicalDevices #EUDAMED #GUDID #MDR #RegulatoryCompliance

[DDi @DDiSmart]

🎆 Happy New Year 2026!

DDi steps into the year driving AI-powered automation, smarter regulatory intelligence, and faster global compliance for life sciences 🌍🤖

Here’s to innovation, efficiency & impact in 2026✨

#HappyNewYear2026 #DDi #LifeSciences #AI #Automation #RegTech

[DDi @DDiSmart]

🎄✨ Merry Christmas from DDi!

Thank you to our partners and teams for driving innovation in regulatory & clinical technology. Wishing you joy, good health & success in the year ahead 🎁🌟

#MerryChristmas #DDi #LifeSciences #RegulatoryTech #AIinHealthcare