Newtopivotaltrial Newtoregistration NewtoPhaseI NMEAZD2389anti-fibrotic NME AZD2389 anti-fibroticmechanismmetabolic dysfunction-associatedsteatohepatitis Additionalindication AZD0486-SOUNDTRACK-B CD19/CD3next-generationbispecificT-cellengagerB-cellnon-Hodgkinlymphoma Life-cyclemanagement EnhertuDESTINY-PanTumor03...
The opportunities for decentralizing clinical trials also bring challenges to an industry often characterized by long cycle times and conservativism. Sponsors and service providers seeking to implement decentralized trials must navigate uncertainties in technology and approach while bala...
This initiative aims to advance the drug development process by enabling clinical trial protocol digitalization, helping to move the industry from a document-centric to a data-centric approach. With this change, Digital Data Flow has the potential to reduce cycle times, improve data reliability and ...
reductions in cycle times More than 465,000 sites activated More than 1,500 sponsors/CROs More than 4,600 studies More than 30 therapeutic areas More than 50,000 users Study startup is key to operational success At the outset of clinical trials, study startup is hindered by inefficient ways...
And a very, very similar trial to the EV studies has been designed looking at sacituzumab given on days 1 and days 8 at 10 mg/kg on a 21-day cycle. And this was in patients, same thing, 2 cohorts, 1 of about a hundred patients, in those patients who had prior platinum therapy...
IQVIA Technologies Clinical Trial Payments is a tech-enabled service offering, independent of IQVIA CRO services, that takes the burden of making payments to sites around the world.
Enhance Your Experience Greenphire Clinical Trial Budgeting Accelerate Study Timelines Remove barriers to timely study startup. Standardizing on Greenphire’s platform simplifies the budget build and negotiation workflow, eliminating unnecessary timeline adjustments and delays, for reduced cycle times. Achieve...
IQVIA Technologies Clinical Trial Payments is a tech-enabled service offering, independent of IQVIA CRO services, that takes the burden of making payments to sites around the world.
Eliminate inefficiencies and reduce contract cycle times by up to 80% Deliver legal and regulatory compliance and transparency reporting requirements Ensure on-time trial execution through proactive tracking of milestones and obligations Reduce cost overruns through proactive monitoring of budget consumption at...
A randomized clinical trial comparing cycle control in a 21-day vs. a 24-day oral contraceptive (OC)By Ronald Burkman MD, Published on 05/01/09Burkman MD, RonaldOb/gyn