Industry events

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

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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

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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"

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Speaker: Arjen Akkerman, Senior Director, Research Services

Session: CMC for ADC

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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

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Speaker: Lucas Miller, Director, Project Management

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

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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.

 

Speaker: Patricia Koochaki, Senior Principal, Patient Centred Outcomes

Friday, 20 October

Session: Clinical Care Applications

Title: Development of an observer reported outcome measure for obstructive sleep apnea

Time: 13:25pm

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Speaker: Martine Dehlinger Kremer, Vice President, Scientific Affairs

Session: DCTs in pediatric trials

 

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Speaker: Martine Dehlinger Kremer, Vice President, Scientific Affairs

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

 

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Speaker: Nina Holst, Executive Director, Alliance Management

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

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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?

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For further information, please visit the conference website.

 

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Speaker: Martine Dehlinger Kremer, Vice President, Scientific Affairs

Session: EMA guidance perspectives on DCTs  

Time: 12:15 - 13:00
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

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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.