Global Clinical Trials Connect Conference 2023: A Platform to Discuss Futuristic Advancements in Clinical Trials and Clinical Research (London, United Kingdom - May 10-11, 2023)

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Apr 13, 2023, 06:45 ET

DUBLIN, April 13, 2023 /PRNewswire/ -- The "Global Clinical Trials Connect 2023" conference has been added to ResearchAndMarkets.com's offering.

The Global Clinical Trials Connect 2023 will provide a platform to discuss on futuristic advancements in clinical trials and clinical research.

This multidisciplinary program involves the broad participation of people from the 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 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 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 healthcare 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.

Who Should Attend:

This event is designed for senior-level attendees from various companies including Pharmaceutical, Bio-Tech, Bio-Pharma, CROs, Investigative Sites, Solution providers and Government institutions.

Key Highlights

Patient Recruitment and Site Selection
Innovative trial designs
Partnership & Collaboration - Sponsors, CROs, Sites and External Vendors
Patient-centric clinical trials
Making Patient Engagement a Reality
New innovations in Patient Recruitment planning and execution on a clinical trial
Outsourcing strategies and models
Electronic Clinical Outcome Assessment and Electronic Patient Reported Outcome
Streamlined IRT development process
Pharmacovigilance & Clinical Trials
Post-Clinical Trial closed communities
How to future proof your clinical operations
Diversity and Inclusion in Clinical Trials
Implementing Risk-Based Monitoring
Streamlining R&D and lower costs in clinical Trials
Adaptive Trial Model
Clinical Trial Auditing
Real-World Clinical Trial Strategies
Data Quality & Technology
Clinical Data Strategy & Analytics
Electronic Data Capture (EDC) Systems
Decentralised Clinical Trials
Clinical Technology and Driving Innovation
M-Health, Wearable and Consumer Technology
Big Data, IoT and Artificial Intelligence in Clinical Trials
Blockchain technology for improving clinical research quality

Attendees include VPs, GMs, Directors, Heads and Managers of

Clinical Trials
Clinical Study Management
Clinical Operations
Clinical Research
Patient Organizations
Patient Recruitment
Outsourcing
Vendor Management
Site Management
Site Monitoring
Clinical Pharmacology
Clinical Data Management
Risk Monitoring
EDC
Clinical/Digital Innovation
Clinical Design/Protocol design/ Strategy makers
Clinical Research Sites
CROs and CMOs
Hospitals/ Associations
Regulatory affairs

Agenda:

Wednesday - 10th May 2023

08:00 - Registration & Refreshments

08:50 - Chairperson's opening remarks

09:00 - Strategies for globalization in clinical trials

09:30 - Stepping up the decentralization of clinical trials

10:00 - Innovative trial designs to save time and cost without compromising on the efficiency

10:30 - Morning Coffee/Tea & Networking

10:50 - Medical Affairs and Clinical Operations collaborating on Clinical Trial Optimization

Patient Recruitment & Site Selection

11:20 - The National Institute for Health Research (NIHR) Patient Recruitment Centres: Optimising patient recruitment to ensure trial success

11:40 - Innovative analytic technologies for predictive modelling, forecasting and optimal designing patient recruitment in clinical trials

12:00 - Monitoring and Quality Assurance in site selection and patient recruitment to optimize clinical trials

12:20 - Networking luncheons

13:10 - The Impact of Diversity Plans on Increasing Overall Enrollment in Clinical Trials

13:40 - Enrolment and retention in clinical studies before and during the Covid-19 pandemic: clinical challenges and new opportunities. A case report from a phase 3 clinical program in fibromyalgia

14:10 - Panel discussion: Critical Success Factors while Planning for Site Selection and Patient Recruitment

14:40 - How Can African Sites be routinely included? Addressing diversity at its core

15:10 - Afternoon Tea/Coffee

Patient Centricity & Patient Engagement

15:30 - Patient Engagement in Clinical Development - A look at what the UK are doing to bring patients to the forefront of study design

16:00 - EU-PEARL: An EU patient-centric clinical trial platform

16:30 - Panel Discussion: Putting the patient first - Embedding a patient-centric approach to clinical trial design

17:00 - Interactive Breakout Discussions

17:50 - Chairperson's closing remarks

18:00 - Networking Drinks Session

Thursday - 11th May 2023

08:30 - Registration & Refreshments

08:50 - Chairperson's opening remarks

09:00 - EHR Case Study: NHS health records in pandemic vaccination programs

09:30 - Global Clinical Development - Complex Generics

09:50 - Setting up Your Decentralised Trial for Success

Clinical Data & Tech-Driven Clinical Trials

10:10 - How Real-World Evidence and Real World Data Can Help Regulatory Agencies Make More Informed Decisions

10:30 - Morning Coffee/Tea & Discussion

10:50 - Improving clinical data management (CDM) and statistics to meet new regulatory requirements

11:10 - Interpretation and Impact of Real-World Clinical Data

11:30 - Trusting Digital Health Technologies: Why Global Standards Are A Must

12:00 - Panel Discussion: The Evolution Of Tech- Enabled Clinical Trials and What to expect from the next decade of drug development

12:30 - Networking luncheon

13:10 - Achieving a streamlined IRT development process

Outsourcing & Clinical Trials

13:30 - Non-enrolling sites: How to early detect them and what to do?

14:00 - Key Considerations for Effective Clinical Trial Vendor Selection

14:20 - How Industry Collaboration is Transforming Clinical Trials

14:50 - A key factor in vendor Selection - The role of the CRO in advancing patient centric clinical trial approaches

15:20 - Afternoon Tea/Coffee

Quality, Compliance & Risk Management

15:40 - Implementing risk proportionate approaches in clinical trials -moving towards risk-based monitoring

16:00 - Are we obsessed with Quality Tolerance Limits?

16:30 - Implementation of Quality by Design (QbD) Principles

17:00 - Panel Discussion - Partnering for progress - How Collaborative partnerships are transforming clinical trials?

17:40 - Chairperson's closing remarks

Speakers

Sarah Tremethick
Global Consortia Program Lead - TransCelerate BioPharma Inc
Roche

Michael Zaiac
Head of Medical Affairs Oncology Region Europe
Novartis

Faidra Van Der Wal
Associate Director Global Development Operations Trial Lead
Janssen Pharmaceutical

Francis Crawley
Executive Director
Good Clinical Practice Alliance - Europe (GCPA)

Maria Palombini
Leader, Healthcare Life Sciences Practice
IEEE Standards Association

Nancy Meyerson-Hess
Chief Compliance and Regulatory Officer
eMQT

Mohamed Sharaf
EMEA Senior Medical Advisor
Janssen Europe, Middle East & Africa

Diane Driver
Head Program Delivery
UCB

Siddharth Chachad
Founder & Chief Strategist
Reguclin Consulting

Richard Evans
Head Of Business Development and Innovation
Leeds Teaching Hospitals NHS Trust

Kate Chapman
Director
Clinical Technology Consultants Ltd

Joanne Stevens
Global Head of R&D Operations
GE Healthcare

Domenico Merante
Clinical Research Lead TA Orphan-Nephrology
CSL Vifor

Gayna B. Whitaker
President and Founder
Genesis Medical Research Group

Nadir Ammour
Global Lead, Clinical Innovation & External Partnership
Sanofi

Alpana Gandhi
Senior Process & Vendor Manager
Boehringer Ingelheim

Viraj Rajadhyaksha
Area Medical Director
AstraZeneca

Tina Barton
Chief Operating Officer
eMQT

Shalom Lloyd
Co-Founder & Chief Strategy Officer
eMQT

Vladimir Anisimov
Principal Data Scientist, Center for Design & Analysis
Amgen

Rebecca Jackson
Sr. Mgr. Clinical R&D Innovation & Novel Modalities IT
The Janssen Pharmaceutical Companies of Johnson & Johnson

Andrew Gray
Global Regulatory and R&D Policy
Amgen

Anthony Mikulaschek
Vice President, eCOA
IQVIA

Natalie Wilson
Business Development Manager
NIHR Clinical Research Network

For more information about this conference visit https://www.researchandmarkets.com/r/mvtzk7

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