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.
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.
HealthTech Insights: Final Rounds of Late-Breaking Clinical Trial Results Announced at VIVA24
The Global Clinical Trials Connect 2025 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.
HealthTech Insights: Equitable Breakthroughs in Medicine Development (EQBMED) to work with Inaugural Sponsor Companies to Drive Greater Diversity in Clinical Trials
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.
The summit will facilitate an invaluable networking opportunities with decision makers and focus on real case studies, insightful presentations and round tables.
HealthTech Insights: Paradigm and Altru Health System Expand Patient Access to Clinical Trials for Rural Population
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
HealthTech Insights: FDA Issues Draft Guidance on Conducting Multiregional Clinical Trials in Oncology
Who Should Attend:
This event is designed for senior level attendees from various companies including Pharmaceutical, Bio-Tech, Bio-Pharma, CRO’s, Investigative Sites, Solution provider and Government institutions.
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
HealthTech Insights: New Clinical Trial Industry Survey Reveals Increased Burdens on Sites
Agenda:
Day 1
- 08:00 Registration & Refreshments
- 08:50 Welcome Address & Chairperson’s opening remarks
- ng Efficiency through Streamlined Clinical Trials
- 09:00 Tactical and Strategic Use of AI in Clinical Trials
- 09:30 Integrating Blockchain into clinical research
- 10:00 Innovating with AI: digital transformations for clinical research
- 10:30 Ensuring Compliance and Inspection Readiness Through Effective Risk Management
- 11:00 Business Card Exchange with Morning Coffee/Tea & Discussion
- 11:20 Forging Successful Global Research Partnership in Southeast Asia – Universiti Malaya Medical Centre’s Experience
- 11:50 Advancing Patient Safety Through Inclusive Clinical Trials: Harnessing Real-World Data Directly from Source
- 12:20 Digital Transformation: Developing and deploying a digital authoring platform across the value chain
- 12:45 Luncheon & Networking – Explore, Engage with Your Peers, and Connect at Our Exhibitor Booths
- 13:35 Increasing diversity in clinical trials in the UK: Results from a nationally representative survey
- 14:00 Patient Involvement and Patient Reported Outcomes. Does it make a difference?
- 14:30 End-to-End management of critical quality factors across a vaccine study/program
- 15:00 From EHR to Sponsor – harnessing electronic health records in clinical research
- 15:30 Recharge with Tea or Coffee While Networking
- 15:50 Panel discussion: Critical Success Factors while Planning for Site Selection and Patient Recruitment
- 16:20 The Role of Investigator-Initiated Trials in Leveraging Real-World Evidence
- 16:50 Sponsor centric to Patient centric framework – Improving patient recruitment & enhancing their involvement
- 17:20 Panel Discussion: The Future of Patient-Centricity in Clinical Trials – Embedding a patient-centric approach to clinical trial design
- 17:50 Interactive Breakout Round Table Discussion
- 18:20 Chairperson’s Closing Remark
- 18:30 Networking Drinks Session – Unwind with Evening Drinks and Engaging Conversations
HealthTech Insights: Amgen to Present Data from Multiple Early-Stage Clinical Trials at Esmo 2024
Day 2
- 08:30 Registration & Refreshments
- 08:50 Welcome Address & Chairperson’s opening remarks
- Shaping the Future with Innovative Trials
- 09:00 Personalized Clinical Trials Framework: Considerations for implementation from a patient centricity perspective
- 09:30 Roche Rater Academy: An enterprise wide approach to developing a rater training lifecycle to improve rater data quality, productivity and inclusivity for an improved customer experience enabled through a strategic supplier partnership
- 10:00 New opportunities for patient recruitment and diversity – Conducting clinical trials in the MENA region
- 10:30 Data-Enabled Recruitment to Clinical Trials and How Real-World Data Can Enhance Clinical Trial Outcomes and Safety Monitoring
HealthTech Insights: Research Solutions Unveils AI Platform for Automated Clinical Trial Landscape Reports
- 11:00 Business Card Exchange with Morning Coffee/Tea & Discussion
- 11:20 Empowering Clinical Research with Artificial Intelligence: Unlocking the Value of Real-World Data
- 11:45 Planning and Placement: A recipe for research delivery success
- 12:15 Smart use of GenAI, NLP and ML in Oncology Clinical Trials
- 12:40 Luncheon & Networking – Explore, Engage with Your Peers, and Connect at Our Exhibitor Booths
- 13:30 How clinical trials can utilise predictive ai to simulate a trial to predict its probability of success, and optimise the variables to increase success probability!
- 13:55 Quality considerations for the use of Real World Evidence in clinical development
- 14:25 Weighing and evaluating the outsourcing approach that is right for you
- 14:55 EU PEARL, platform trials
- 15:25 Recharge with Tea or Coffee While Networking
- 15:45 Africa’s role in reducing clinical delays
- 16:15 Interpretation and Impact of Real-World Clinical Data
- 16:45 Panel Discussion: Leveraging Big Data and AI in the Era of Tech-Driven Clinical Trials: Opportunities and Ethical Dilemmas
- 17:15 Partnership & Collaboration – Sponsors, CROs, Sites and External Vendors
- 17:40 Chairperson’s Closing Remark
To participate in our interviews, please write to our HealthTech Media Room at news@intentamplify.com
Source – globenewswire
