Global Clinical Trials Connect Conference 2022: Futuristic Advancements in Clinical Trials and Clinical Research - September 21-22, 2022
11 Jul 2022
Generic DrugAcquisitionCollaborate
DUBLIN, July 11, 2022 /PRNewswire/ -- The 'Global Clinical Trials Connect 2022' conference has been added to
ResearchAndMarkets.com's offering.
The Global Clinical Trials Connect 2022 will provide a platform to discuss on the futuristic advancements in clinical trials and clinical research.
This multidisciplinary program involves broad participation of people from clinical trials community from around the globe who are focused on learning more about clinical research, clinical trials planning and management.
The Pharma and Bio-Tech companies are consistently evolving and new clinical studies, technologies and advancements in care and treatments have augmented the efficiency and at the same time, the complexity of clinical trials has increased, with tests being carried out in a highly structured and closely coordinated manner. It is high time that we look into innovative strategies, new technologies, effective and quality collaborations to address these issues, which can cater to the needs of the patient and the industry.
This conference intends to focus on the global health and clinical trials around the world. Bioethics, regulations, patient recruitment, site selection, real-world data, data integration & Strategy, outsourcing, vendor management, quality (QbD) in Trial Conduct, risk-based monitoring, clinical auditing & financial planning and other significant topics that play a key role in clinical trials will be addressed along with innovative sessions on new technologies, effective and quality collaborations.
This program will certainly educate health care scientists on trial design, operations, organizing trials, research computing, regulatory aspects, report on clinical trials and gain a better knowledge of the implications of clinical trials in prevention, diagnosis, clinical trial-related ethics and disease treatments.
The summit will facilitate an invaluable networking opportunities with decision makers and focus on real case studies, insightful presentations and round tables.
Agenda:
Day 1 - Wednesday - 21st September 2022 (Time Zone - BST)
09:30 - Welcome Address & Platform Orientation - Orientation will focus on how to access and navigate the virtual conference platform for Live Sessions & Interactive Networking
09:40 - Chairperson's opening remarks
Nancy Meyerson-Hess Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
eMQT
09:50 - Transforming the Way We Do Clinical Trials: Pragmatic Trials Combined with EHR Enabled Services
Mats Sundgren Mats Sundgren Director Health Informatics
10:15 - Novel approaches in Clinical Trial Design to Improve Efficiency of Research
Strategies & Methods for flexible design trials
The Adoption and Impact of Adaptive Trial Designs
Preclinical environment and trial designs Opportunities and Limitations
10:40 - Learnings from a Fully Decentralized Trial in Oncology and a Hybrid Decentralized in Autism
Connecting the developed and the developing nations
Dealing with differences owing to culture and ethnicity
Role of CROs and third party stakeholders
Thomas Wiese Thomas Wiese Principal Medical Director, Clinical Expert Team Leader
11:05 - How the World Health Organization's International Clinical Trials Registry Platform (ICTRP) is improving research transparency globally.
Ghassan Karam Ghassan Karam Project Manager
World Health Organization
Patient Recruitment & Site Selection
11:30 - How Digital recruitment is changing the face of clinical trials
Livia Dixon Livia Dixon Director Digital Recruitment Strategist
11:55 - Innovative technologies for data-driven predictive modelling, forecasting and optimizing patient recruitment in clinical trials
Advanced technologies to maximize patient recruitment predictability at different stages
Forecasting recruitment under different restrictions
Optimal time-cost efficient recruitment design, sites / countries selection
Centralized statistical monitoring and detecting unusual data patterns
Forecasting future recruitment performance
Vladimir Anisimov Vladimir Anisimov Principal Data Scientist, Data Science, Center for Design & Analysis
12:20 - Virtual Luncheon & Networking - Visit Exhibitor Booths & Network with your peers in our Lounge (Face to Face Video Chats)
13:00 - Monitoring and Quality Assurance in site selection and patient recruitment to optimize clinical trials
Site pre-assessment and selection
Ensure patient protection and to deliver high quality data
Quality assurance can at times be difficult as regulatory requirements, standards and access to care differ globally - How are we going to handle this?
13:25 - Feasibility in clinical trials
Importance of conducting feasibility
The stages of clinical trial feasibility
Feasibility challenges
Dex Bilkic Dex Bilkic Manager, Study Start-up, Patient Recruitment and Outsourced Studies
13:50 - How can clinical research be truly patient centric?
The Journey of Bringing the Voice of Patients and Sites into End-to-End Clinical Development
Bert Santy Bert Santy Patient and Site Engagement Lead
14:15 - Panel discussion: Effective patient recruitment and retention in clinical trials to boost trial success
What will persuade and impact the patient?
Is there anything pharma can provide for a trial member that will increase the value of participation?
The aim of patient-driven clinical trials is to diminish the burden of participation by making the participant journey as convenient and pleasant as possible
Utilize fitting procedures and techniques to limit dropouts without, in any capacity, constraining a patient to remain in the study
Dex Bilkic Dex Bilkic Manager, Study Start-up, Patient Recruitment and Outsourced Studies
Nancy Meyerson-Hess Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
eMQT
14:40 - Harnessing the power of Deep Site Data and AI to advance clinical trials - Gain insights that would not be possible with traditional approaches
Patient Centricity & Patient Engagement
15:05 - Bringing the patient voice in the design of clinical trials and how patient engagement/inclusiveness must be planned and implemented throughout the lifecycle of clinical development
Lea-Isabelle Proulx Lea-Isabelle Proulx Patient Voice Partner
15:30 - Visit Virtual Exhibitor Booths/Speed Networking at our Exclusive Lounge (Face to Face Video chat with Exhibitors and other attendees)
15:50 - Patient partnering strategies in clinical research
Patient partnership models to assist researchers assess which method of engagement could work best
Active role in setting research priorities
Patient associations leading research projects
16:15 - Multistakeholder approach from the patient perspective
A session on the multistakeholder contributor network that is the basis behind 'Patient Focused Medicines Development' initiatives
Carole Scrafton Carole Scrafton Patient & Health Advocate
FibroFlutters
16:40 - Global Clinical Development - Complex Generics
Siddharth Chachad Siddharth Chachad Executive Vice President & Head - Global Clinical Management
Dr. Reddy's Laboratories
17:05 - The patient's perspective: why their voice is so important in clinical research
Nancy Meyerson-Hess Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
eMQT
Mary Lynne Van Poelgeest-Pomfret Mary Lynne Van Poelgeest-Pomfret International patient advocate
World Federation for Incontinent Patients - WFIP
17:30 - Interactive Breakout Discussions:
All the participants will have a great opportunity to discuss and explore a selection of most interesting topics discussed during the conference in small groups with their industry colleagues in an informal setting.
Round Table 1: Innovation in Clinical Trials - Digital Approaches
Round Table 2: Patient Centricity
Round Table 3: Globalization and Country Specifics
Round Table 4: Recruitment Challenges - Patients and Sites
Round Table 5: Changing Clinical Trials - What needs to be addressed
Round Table 6: Patient Retention
18:00 - Chairperson's closing remarks
Nancy Meyerson-Hess Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
eMQT
18:10 - Networking Drinks Session
Day 2 -
Thursday - 22nd September 2022 (Time Zone - BST)
09:30 - Welcome Address & Platform Orientation - Orientation will focus on how to access and navigate the virtual conference platform for Live Sessions & Interactive Networking
09:40 - Chairperson's opening remarks
Nancy Meyerson-Hess Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
eMQT
09:50 - Topic TBC
Rebecca Jackson Rebecca Jackson Sr. Mgr. Clinical R&D Innovation & Novel Modalities IT
10:15 - Enrolment and retention in clinical studies before and during Covid-19 pandemic: clinical challenges and new opportunities. A case report from a phase 3 clinical program in fibromyalgia
Domenico Merante Domenico Merante Global Clinical Development TA Lead Nephrology and Orphan Disease Area
Decentralized Clinical Trials
10:40 - Exploring Decentralised and Virtual trials, with pilot studies and challenges encountered
Michael Zaiac Michael Zaiac Head of Medical Affairs Oncology Region Europe
11:05 - Optimizing your Decentralized Clinical Trials with Real-World Data
11:30 - Setting up Your Decentralised Trial for Success
New business model based on the Technological advances and research activities integrated seamlessly into clinical trials
Developing custom made contracts by third-party vendors, CROs and sponsors for modern clinical trials
Angel Soubhie Angel Soubhie Head clinical trial scientists - Medical Director
Outsourcing & Clinical Trials
11:55 - A key factor in vendor Selection - The role of the CRO in advancing patientcentric clinical trial approaches
Jan Schmejkal Jan Schmejkal Associate Director, Clinical Project Lead
12:20 - Virtual Luncheon & Networking - Visit Exhibitor Booths & Network with your peers in our Lounge (Face to Face Video Chats)
13:00 - Panel Discussion - A collaborative clinical ecosystem: How to effectively manage partnerships with all Stakeholders including Patients, Sites, CROs, Sponsors and Regulators.
Nancy Meyerson-Hess Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
eMQT
Sonia Houston Pichardo Sonia Houston Pichardo Business Lead of MyStudyWindow
Quality, Compliance & Risk Management
13:30 - The effectiveness of new generation analytics models in RBM
Centralized monitoring can characterize key risk classifications and pointers from all clinical and operational source data available.
To evaluate risks to site performance, subject safety and data quality using Data and Analytics
Differentiating the relative risks between sites and subjects using the new age analytics models.
Shawntel Swannack Shawntel Swannack Director, Central Monitoring and Data Analytics
13:55 - Implementing risk based approaches within clinical trial
Laura Galuchie Laura Galuchie Senior Director & TransCelerate Program Lead
Merck
14:20 - Are we obsessed with Quality Tolerance Limits?
Choosing QTL Parameters wisely
Are you asking the right questions when considering the application of Quality Tolerance Limits (QTL)?
Controlling risk within diagnostic clinical studies
Mireille (Zerola) Lovejoy Mireille (Zerola) Lovejoy Director of Clinical Risk Management
Clinical Data & Tech Driven Clinical Trials
14:55 - FDA draft guidance on 'Digital Health Technologies for Remote Data Acquisition in Clinical Investigations
Benoit Marchal Benoit Marchal Senior IT Project Manager (PMP)
F. Hoffmann-La Roche AG
15:20 - Visit Virtual Exhibitor Booths/Speed Networking at our Exclusive Lounge (Face to Face Video chat with Exhibitors and other attendees)
15:40 - Interpretation and Impact of Real-World Clinical Data
Strategies for better decision-making
High-level models and simulations compelled by data will allow elimination of risky trials
The potential of real world data in clinical research goes past patient identification and patient recruitment
Mohamed Sharaf Mohamed Sharaf EMEA Medical Program Lead (Immunology)
Janssen Europe, Middle East & Africa (EMEA)
16:05 - Clinical trials in the era of digitization - the impact of smart innovations in clinical research
Rethinking the R&D Clinical Process
Patient-Centred Innovation in Clinical Trials
New trial designs and analysis methods
Discovering and validating sequential, personalized decision-making strategies
An Integrated Business Model - Using technology to streamline processes
Maria Palombini Maria Palombini Leader, Healthcare Life Sciences Practice
IEEE Standards Association
16:30 - Leverage AI to create value in Clinical Trials
16:55 - Panel Discussion: The Future of Clinical Trials - The Role of Advanced Analytics and Artificial Intelligence
Mohamed Sharaf Mohamed Sharaf EMEA Medical Program Lead (Immunology)
Janssen Europe, Middle East & Africa (EMEA)
Bhupathy Alagiriswamy Bhupathy Alagiriswamy Director
Credence Clinical Solutions Ltd
Nancy Meyerson-Hess Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
eMQT
17:25 - Novel techniques- Tech-driven clinical trials
Effectively using Technology is enabling patient centricity
How to implement mobile technology and make it work in clinical trials
Does consumer technology devices used in clinical trials?
IoT in digital transformation of clinical trials
17:50 - Integrating Blockchain into clinical research
Uses & challenges for Blockchain in Clinical Trials
Storing all types of data safely and securely
Better Clinical Trials Quality
18:15 - Chairperson's closing remarks
Nancy Meyerson-Hess Nancy Meyerson-Hess Chief Compliance and Regulatory Officer
eMQT
For more information about this conference visit https://www.researchandmarkets.com/r/dan7e2
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