Archives: Agenda
KEYNOTE PRESENTATION: Establishing a Center of Excellence for gene therapy and vaccines
PANEL: Navigating the outsourcing landscape for emerging therapy areas
- An overview of emerging therapy areas including women’s health, cell and gene therapy and rare diseases
- Designing a successful patient recruitment strategy: common challenges and how to overcome these
- Vendor sourcing: key considerations in vendor selection
- How important is therapeutic area knowledge when choosing CROs and partners?
The state of the biopharmaceutical industry in 2025: emerging technologies and opportunities
- Emerging themes and technology advancements in biopharma
- Leveraging data to predict the outlook for 2025 clinical trials
- Trends, key players, opportunities, and threats in clinical trial outsourcing
- Latest biopharma investor activity: venturing financing, IPOs, and grants
PROBLEM-SOLVING ROUNDTABLE DISCUSSIONS
During the roundtable discussion session, the conference hall will be divided into four ‘zones’. Delegates can choose which zone they would like to join. Each zone will focus on a different challenge within clinical operations.
ROUNDTABLE 1: Developing a successful Diversity Action Plan for your clinical trial
ROUNDTABLE 2: Creating an AI strategy to support clinical research
ROUNDTABLE 3: Key considerations when selecting a CRO
ROUNDTABLE 4: Working with advocacy groups to keep the patient voice at the heart of your trial
Health literacy in clinical trials: ensuring information is clear and accessible to patients
- Technology and innovation for addressing health literacy and how information is presented to patients
- Integrating health literacy principles into all phases of clinical research
- How low health literacy can
End of conference
NETWORKING DRINKS RECEPTION SPONSORED BY GLOBALDATA
CASE STUDY: Getting a new site up and running: challenges, opportunities and lessons learned
- Top tips for working with and supporting naïve physicians in order to ensure their success
- The importance of new study sites as a way of meeting FDA diversity requirements
- Lessons learned for the future: what should you consider when working with naïve doctors?
Carrie Lewis, Executive Director, Clinical Program
Optimization, Endo
Suzy Montanye, Site Relationship Manager, Endo
Achieving submission excellence with Certara’s regulatory operations solutions
- Defining the full lifecycle of clinical and regulatory documents
- Identifying practical actions authors can take to facilitate compliance with electronic regulatory submission requirements
- Describing how technology tools are used to ensure efficient workflows and regulatory compliance