The Pharma & Bio Pharma industry is rapidly moving towards end-to-end drug accountability in clinical trials as there is a need to track the receipt of a drug from shipment to dispensing, return and destruction. The IRT continues to gain momentum as a critical component to clinical trial and supply chain strategy, and as the complexity of trials continues to rise, optimizing the IRT is paramount.
Join DDi at IRT 2016 – CBI’s Interactive Response Technologies in Clinical Trials on OCTOBER 25-26, 2016 at HILTON AT PENN’S LANDING in PHILADELPHIA, PA. DDi’s mIRT provides the ideal Lean, Faster, Cost Efficient tool for clinical supply management.
Detailed supply management functionality coupled with both ivrs and iwrs randomization functionality. No bulky workflows and unwanted bells & whistles. Completely LEAN
FASTER Implementation : UI based configuration leading to less startup time and lesser QA times