Global Clinical Trials Connect 2024

The Global Clinical Trials Connect 2024 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 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 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 invaluable networking opportunities with decision makers and focus on real case studies, insightful presentations and round tables.

It gives us great pleasure in welcoming you to the Global Clinical Trials Connect 2024.

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

Who should attend the conference?
Attendees includes 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