Industry events

Session: Chair’s Opening Remarks;

Speaker: Emily Mitchell

Time & date: 13 September - 9:30am

Session: Turning Clinical Research to Virtual Capacity

Speaker: Madelaine MacKay 

Time & date: 13 September - 11:40 am

Session: Develop and Action: What Can We Learn About the Gold Standard for DCT Planning & How Can We Mirror This?

Speaker: Madelaine MacKay 

Time & date: 13 September - 12:20pm

For further information, please visit the conference website.

 

For further information, please visit the summit website.

 

Speaker: Brian Greene, VP, Business Development

Panel: Temperature Check: How are Mobile and Digital Technologies Enabling Traditionally Underrepresented Communities to Participate in Clinical Trials?

For further information, please visit the conference website.

 

Speakers: Adam Halbridge, Executive Director, Medical Safety Services *with client - Lucinda Orsini, Compass Pathways

Session: Collaborating to transform the shape of clinical development - Clinical Trial Tokenisation

For further information, please visit the conference website.

 

Panelist & Session: Tanja Obradovic, Vice President, Scientific Affairs, ICON

Session title: Optimising early development to maximize success probability in the late stage development

Panel: What we as an industry need to do to promote trust

Time & date: 11:30am on Day one of Stream B (Clinical Trial Technology & Innovation)

For further information, please visit the conference website.

 

Speaker: Rebecca Rozich, PhD, ISMPP, CMPP Director, Client Engagement & Medical Strategy ICON Global Medical Communications

Session: Beyond the Traditional Publication Plan

For further information, please visit the conference website.

 

Speaker: Melissa Gottschlich, Director, Clinical Operations Accellacare

Panel: Regulatory & FDA Guidance on Diversity, Equity & Inclusion: What Sites & Industry Need to Know

Speaker: April Coburn

Session: Understanding Different Site Operation Models: Balancing Relationships & Success for Growth

Time & date: Saturday, October 7 at 4:15 pm - 5:15 pm

For further information, please visit the conference website.

 

Speakers: Stephen Cameron & Alejandra Calcagno

Session: "Getting the "science of clinical trials" into the data scientist role."

Speaker: Kimberly Dley

Session: "Improving Patient-Centricity & Choice with Digitally Connected Trials: The true DCT" and "Getting the "science of clinical trials" into the data scientist role."

Speaker: Tanya Sun

Session: "Project Management Superheroes behind Study Build"

Speaker: Kenneth Stoltzfus

Session: "Workshop: Data Requirements for an FDA Submission"

Speaker: Emily Mitchell

Session: "Community Collaboration: Leveraging Existing Networks to Increase DCT Access for Rural Populations"

Speaker: Stephen Cameron

Session: "Leadership Mash Up" and "SCDM Awards & Closing keynote"

For further information, please visit the conference website.

 

For further information, please visit the conference website.

Speaker: Arjen Akkerman, Senior Director, Research Services

Session: CMC for ADC

For further information, please visit the conference website.

 

Speaker Session 1: Dimitar Karzhin, Director Clinical Trial Management & Dinah Knotts, Vice President, Project Management, Vaccines and Infectious Diseases

Session: Interactive Roundtable: Engaging with sites to increase diversity in clinical tirals

For further information, please visit the conference website.

 

Speaker: Lucas Miller, Director, Project Management

Interactive session: Should Temperature Excursions (TE) be Captured in the IRT?

For further information, please visit the conference website.

 

Speakers: Kirsten Sherman Cervati, Senior Director, Therapeutic Area and Martine Dehlinger-Kremer, Vice President, Scientific Affairs

Tuesday, 17 October

Session: Opening of the conference and Introduction

Time: 10:30am

Speaker: Martine Dehlinger-Kremer, EFGCP, EUCROF

 

Wednesday, 18 October

Session: Welcome and Debrief from Day 1

Time: 08:30am

Speaker: Martine Dehlinger-Kremer, EFGCP, EUCROF

Session: The Enpr-EMA Initiative on Site Quality Criteria/ Standards for Paediatric Trials

Time: 08:45am

Speaker: Kirsten Sherman Cervati

Session: Paediatric formulation development between patients’ needs, methodology and regulatory requirements

Time: 11:30am

Speaker: Martine Dehlinger-Kremer, EFGCP, EUCROF

Session: End of Day 2 - Conclusion and Farewell

Time: 16:15pm

Speaker: Martine Dehlinger-Kremer, EFGCP, EUCROF

 

For further information, please visit the conference website.

 

For further information, please visit the conference website.

 

Speaker: Martine Dehlinger Kremer, Vice President, Scientific Affairs

Session: DCTs in pediatric trials

 

For further information, please visit the conference website.

 

Speaker: Martine Dehlinger Kremer, Vice President, Scientific Affairs

Session: Presentation at the seventh session of the Human Medicines Symposium, HM7: Paediatric Investigational Plans

 

For further information, please visit the conference website.

 

Speaker: Nina Holst, Executive Director, Alliance Management

Join presentation with LEO Pharma:  "Building a flexible and efficient clinical operation organisation through a strategic partnership"

For further information, please visit the conference website.

 

For further information, please visit the conference website.

 

For further information, please visit the conference website.

 

For further information, please visit the conference website.

 

Speaker: Missy Hansen, Associate Director             

Session: Assessing risk in your clinical trial using the Pediatric Risk Assessment Map (PRAM)

Panel discussion: Is DCT old news?

For further information, please visit the conference website.

 

For further information, please visit the conference website.

 

For further information, please visit the conference website.

 

For further information, please visit the conference website.

 

Speaker: Martine Dehlinger Kremer, Vice President, Scientific Affairs

Session: EMA Guidance Perspectives On DCTs

 

For further information, please visit the conference website.

 

For further information, please visit the conference website.

 

For further information, please visit the conference website.

 

For further information, please visit the conference website.

 

Speaker: Alexandre Malouvier, Senior Director, Therapeutic Area

Session: AI is already transforming clinical research and not everyone is prepared

For further information, please visit the conference website.

 

For further information, please visit the conference website.

 

Speaker: Martine Dehlinger Kremer, Vice President, Scientific Affairs

Session: 24 November: BVMA symposium, moderation of session CTR/ CTIS

 

For further information, please visit the conference website.

 

For further information, please visit the conference website.

 

For further information, please visit the conference website.