Key Agenda Highlights
The Clinical Trial Supply Southern California event will give a well-rounded view to address the key challenges in regards to navigating the clinical trial supply landscape to ensure timely trials.
Clinical trial supply can be complex and is critical in the overall success of your study. The content covered in our agenda will help create robust clinical trial supply strategies to tackle the full spectrum of associated challenges.
Some key agenda highlights are:
Establishing how the industry is forecasting to help balance drug supply and demand to ensure timely clinical trials:
- Our keynote speaker Pratik Ahuja from Amgen is going to shine a spotlight on how to forecast effectively to help adhere to timelines
The Small Pharma / Biotech commercialization dilemma – go at it alone, partner, or divest via acquisition:
- Join our debate on the key question for the San Diego biotech hub, we have both small and larger pharmaceutical companies represented to give the full view point
Addressing the falsified medication legislation in the EU and how it impacts comparator sourcing for your trial:
- Hear the updates in the falsified medication legislation to ensure you avoid the common pitfalls and noncompliance delays
Addressing the critical factors during your study which impact your clinical trial supplies:
- Our panelists will be creating an interactive environment to compare clinical trial implications and how to modify trial supplies accordingly
Evaluating the outcome of Brexit and the impact of clinical trial supply both in the UK and the EU to avoid increased cost or delays:
- Brexit has potential to disrupt your clinical trial supply, however we will come together to discuss the best plan of action to mitigate impact to your clinical trial supply
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