Bootstrap Main Menu
DDi - eClinical Tools & Solution provider for data management in clinical trial
For Labeling Teams, What Does 10 Minutes Saving Per Day Means?
Most Common and Avoidable Mistakes While Adopting ISO 13485
Regulatory Data and Info management for Med Device success
Effectiveness and Flexibility of Adaptive Designs in Clinical Trials
Labeling of Pharmaceutical Products
Effective Regulatory Change Management with Reg Intel Equipped RIM Tech
Top Trends of Enterprise Labeling in 2019
Reg Information/Data for Devices, very important going forward!
Integration & Reconciliation IRT Guidelines
Technology Towards An Efficient Monitoring Of Clinical Trials
Bulk/Non-Uniquely Number Kits in a Study
We are Direct to Subject Ready
Clinical Trial Supplies Accountability
Digitize Instructions for Use (IFU) to Comply with EU MDR
Clinical projects (you or your vendors/CROs) are putting them at Risk by 80%...
Why Combining Performance, Oversight, Risk and Compliance are very important for your Clinical Development?
Why sponsors should opt Configurable IRT system, before opting any custom version?
Are You Aware of Other Countrie's Regulatory Requirements?
Start small and smart with Labeling Automation
How are you managing your medical devices Regulatory Information?
Data Integrity in Clinical Trials & IRT
Labeling Digitization Manage Data, not Documents
Clinical Supply Strategies to Avoid Overages & Stock Outs
5 Ways Regulatory Data Can Drive Performance
Labeling findings from FDA and other Agencies audits summary
Why RIM is Important for Medical Device Companies
FDA UDI Vs EU UDI
CDISC Standards For BA/BE Studies
Clinical Governance & Oversight: what is the challenge?
Risk Assessment in Clinical Trials
Risk Assessment In Clinical Trials - Well Begun Is Half Done
Constraints in Clinical Trial Supply Chain Management
Handling Missing Data in Clinical Trials
eCRF design best practices
Risk Based Monitoring Path Forward
BIG DATA Pharmaceutical Industry
Reconciling EDC & Safety Systems
Electronic Drug Accountability through IRT Systems
Medical Device Regulatory systems
NEWS & EVENTS
2 of Global TOP 10 Biopharma companies selected REGai for Regulatory Automation
DDi Opened new Data center in Frankfurt, Germany
A fast-growing Mid-Level (public stock listed USA) company selected mIRT XPRESS
TULA recognized as “The 10 Most Trusted Risk and Compliance Solution Providers”
DDi’s Patent-pending LABELai has New Version for Cloud to Address Labeling Challenges Effectively
Global TOP 5 Pharma Company Awarded Regulatory Automation to DDi
TOP 100 Global Pharma company selected mIRT
Mahesh Malneedi from DDi speaking on tools and technology in clinical data analysis at ITCT2017 Congress
DDi winner of Global Excellence in Life Science Technology by Corporate LiveWire
DDi recognized as eclinical global leader by Silicon Review Magazine USA
DDi released next version of TULA with oversight features
Asia Pharma major selected TULA & CM for Oversight and RBM
Role of Integrated systems in Clinical Research, at ACDM conf by Mahesh Malneedi
DDi among the Top 10 Clinical Data Management Solution Providers
A Fast Growing US Pharma Client selected DDi for CDM Solutions & eClinical tools
Princeton inviting DDi
DDi the Finalist in 2015 Clinical Informatics Award
DDi recognised as Finalist in "the 2015 Clinical Informatics News Best Practices Award "
Visit DDi at 27th Annual EuroMeeting & 8th Annual Clinical Forum, DIA Europe on April 13-15 in Paris
Mahesh Malneedi speaking at D2D (Data to Drugs and Diagnostics) Edison, NJ on June 11, 2014
mEDC wins multi-year contract with a Top 20 Pharmaceutical company
CDM & Big Data Leaders Forum 2013, Basel, Switzerland
USA based Biomedical company selected mEDC and mIRT in Q3, 2013
mEDC and mCODER newer versions at SCDM in Chicago
MakroCare Exhibiting at Clinical Outsourcing World Europe 2013 in London
Company Name :
E-mail Id :
Phone No :
Recaptcha Word Verification:
NEWS & EVENTS
4 Independence Way
Princeton, NJ 08540
Tel: (877) 877-1519
Copyright Ⓒ 2020 DDi. All rights reserved.