- Enhancing real-time data visibility and accuracy
- Streamlining compliance and regulatory adherence
- Boosting flexibility and efficiency in clinical supply management
- Highlighting the key changes in ICH E6 (R3) and their practical implications for clinical trial conduct
- Exploring approaches to implementing new guidelines in diverse trial settings
- Analysing challenges, opportunities, and interpretations associated with ICH E6 (R3)
- Sharing actions taken so far to comply with latest updates
- How AI optimizes clinical trial protocols to reduce errors, streamline processes, and enhance data quality
- A Real-world case study of reduced timelines and improved trial outcomes using Biorce’s platform
- Insights into leveraging predictive analytics for trial success
- Sharing issues and feedback collated regarding difficulties of trials in EU
- Discussing potential solutions to improve the appeal of running trials in EU
- Looking at how and when these solutions could be implemented
- Track budgets in sync with timelines using a simple Excel-based model
- Forecast cash flow and spot issues early — no finance degree needed
- Boost transparency between sponsors and vendors, reduce surprises
- Weighing up pros and cons of different outsourcing models: which is best for your trial?
- When is mixing and matching better than fully outsourcing or keeping trials fully in house?
- Developing an outsourcing strategy with limited resources
- Why is FSP becoming a popular choice among sponsor companies and how can this support meeting trial timelines?
- How do strategic alliances impact this decision?
