IDDI Newsletter – July 2023

IDDI Newsletter July 2023

NEWSLETTER – JULY 2023

ALL THE TEAMS AT IDDI WISH YOU A WONDERFUL SUMMER!

Take a break and enjoy some insightful content we are happy to share with you.


IDDI Achieves Accreditation in Medidata Rave EDC

NEWS & EVENTS

IDDI ACHIEVES ACCREDITATION IN MEDIDATA RAVE EDC 
“Achieving the Medidata Rave EDC accreditation demonstrates IDDI’s dedication to offering our customers an optimal EDC solution. We are confident that in aligning with industry leaders like Medidata, we can deliver the highest level of quality and trusted data for our customers across all trial phases, complexity and therapeutic areas”, says Serge Bodart, CCO IDDI.
Read the full Press Release

eBook: The Ultimate Guide to Clinical Data Management

eBOOK

eBOOK: THE ULTIMATE GUIDE TO CLINICAL DATA MANAGEMENT 
This eBook is a must-read that will enable clinical professionals to better understand the Clinical Data Management (CDM) processes involved in a clinical trial to ensure clinical data is ready for submission.
Download Here

LEARN MORE ON OUR CLINICAL DATA MANAGEMENT SERVICES


On-Demand Webinars

ON-DEMAND WEBINARS

WHY DO SO MANY PHASE III TRIALS FAIL? 

Learn about statistical explanations for a large proportion of Phase III clinical trials failures, and how to address both the overestimation of treatment effects, and the misinterpretation of P-values via Bayesian methods.

Listen to the recorded webinar
THE ADDED VALUE OF BIOSTATISTICS-DRIVEN RANDOMIZATION & TRIAL SUPPLY MANAGEMENT SYSTEM

In this joint IDDI/CLARIO case study-focused webinar, the  speakers demonstrated  how biostatistics is crucial at multiple stages of clinical trials such as study design, randomization implementation, rerandomization needs, randomization and drug supply checks, unblinding and final analysis.

Listen to the recorded webinar
GPC – A NOVEL STATISTICAL METHOD FOR OUTCOME ANALYSIS AND REPORTING OF PRIORITIZED COMPOSITE ENDPOINTS

Learn how the Generalized Pairwise Comparisons – GPC method can be used to design clinical trials with multiple endpoints. You will also understand the differences between the GPC treatment effect measures: the net treatment benefit, success odds and win ratio.

Listen to the recorded webinar

ALL THE RECORDINGS AND PRESENTATIONS OF OUR WEBINARS ARE AVAILABLE ON OUR IDDI WEBINAR WEBPAGE.


GPC Podcast - A Novel Statistical Method for Outcome Analysis and Reporting of Prioritized Composite Endpoints

PODCAST

GPC – A NOVEL STATISTICAL METHOD FOR OUTCOME ANALYSIS AND REPORTING OF PRIORITIZED COMPOSITE ENDPOINTS

Learn how the Generalized Pairwise Comparisons – GPC method can be used to design clinical trials with multiple endpoints. You will also understand the differences between the GPC treatment effect measures: the net treatment benefit, success odds and win ratio.

Listen to the Podcast

Optimizing Your Clinical Development Strategy

OPTIMIZING YOUR CLINICAL DEVELOPMENT STRATEGY 

  • Aiming at optimizing your clinical development strategy, IDDI consultants provide expert advice in clinical trial, regulatory statistics and innovative approaches to design optimal development programs with the greatest potential for commercial success and improved patient outcomes.

  • Our Consultant Team provides support at the Regulatory Authorities (FDA/EMA): statistical input is often critical for regulatory interactions, either to discuss specific statistical analyses or to assess statistical implications of clinical trial designs or clinical development programs. 

Discover our Clinical Development & Regulatory Statistical Services

Welcome to Our New Consultant, Vincent Staggs, PhD

SPOTLIGHT ON THE STATISTICAL CONSULTING AND RESEARCH TEAM 

WELCOME TO VINCENT STAGGS, PhD 

We are happy to welcome Vince in the Statistical Consulting & Research team as Senior Scientist and excited to see the team grow and expand to the US.

Vince has a M.S. in Mathematics from Missouri State University and a PhD in Quantitative Psychology from the University of Kansas. He previously served as the Director of the Biostatistics & Epidemiology Core at Children’s Mercy Research Institute and as a faculty member of the School of Medicine at the University of Missouri-Kansas City. Some areas of his expertise include Bayesian hierarchical modeling, clinical trial design, and psychometrics. 


Conferences & Meetings

CONFERENCES & MEETINGS

We look forward to meeting you at conferences to discuss your needs for your upcoming trials.  We combine advanced biostatistics, regulatory and medical expertise, and innovative integrated eClinical solutions to increase efficiency and mitigate risks throughout the drug development process. 

  • 11- 12 JULY  ARENA: Clinical Operations in Oncology Trials East Coast – Boston   Booth # 15Meet Shruti Jituri and Kalyn Dozier 
  • 3-7 SEPT: CEN (Central Europan Network Conference) –  Basel, Switzerland  | Meet Erik Falvey 
  • 26-27 SEPT: ARENA: Outsourcing in Clinical Trials Southern California, La Jolla  Meet Shruti Jituri 
  • 26 SEPT: Bioforward – Oxford, UK | Meet Erik Falvey

 


HR News

HR NEWS

WE KEEP ON GROWING – WE KEEP ON HIRING!
 
We are looking for talents to join our growing team in Belgium and the USA! Are  you ready for new challenges in helping biotech and pharma companies develop new drugs and treatments? Apply today!
 
JOIN OUR INNOVATIVE AND GROWING TEAM – WE ARE HIRING!
Check out our open positions

Well-Being & Fun at IDDI

“Well-being is the experience of health, happiness, and prosperity. It includes having good mental health, high life satisfaction, a sense of meaning or purpose, and the ability to manage stress. More generally, well-being is just feeling well”. Definition from Berkeley Well-being Institute.

IDDI strives to promote a healthy work-life balance and  encourages self-care, self-compassion and self-advocacy.  

Yoga Sessions in the IDDI Gardens
YOGA SESSIONS IN THE IDDI GARDENS 
Beach Volley
BEACH VOLLEY 
Barbecue in the IDDI Gardens
BARBECUE IN THE IDDI GARDENS

ABOUT IDDI :  BIOSTATISTICS & CLINICAL DATA SCIENCE EXPERTS 

Founded in 1991, IDDI is an expert clinical data services and high-level strategic  consulting contract research organization offering Trial Design – Randomization – Data Management and Biostatistics services for Pharmaceutical,  Biotech & medical device/diagnostic  companies.  

ANY UPCOMING RFP/RFI? 
CONTACT US