expertXchange Webinar: Pre-IND and Distribution Strategies – Ensuring Efficient Clinical Studies

Navigating the complexities of early-phase clinical trials requires strategic foresight and regulatory expertise.

PCI Pharma Services, with over 50 years of experience in delivering life changing therapies, invites you to an exclusive webinar focused on optimizing Pre-IND strategies and distribution planning to accelerate clinical trial timelines.

Date: May 6th, 2025 
Time: 8am PT | 11am EDT | 4pm GMT | 5pm CEST 

Join our industry experts, Sharlett Burgess and Zach Rupert, as they share invaluable
insights on:

• Pre-IND Strategy & Regulatory Considerations – How proactive planning can reduce First Patient-In (FPI) timelines by 6-8 weeks and streamline the IND submission process.
• Leveraging a Canadian CDMO – Understanding the benefits of importing, labeling, and packaging clinical trial materials in Canada to enable immediate shipment post-IND approval.
• Global Depot & Distribution Strategies – Overcoming supply chain complexities with a tailored approach for different regulatory environments worldwide.
• Risk Mitigation & Compliance – Addressing potential challenges in Pre-IND packaging, import/export logistics, and evolving global trade & tariff regulations.

This webinar will help you enhance your clinical supply strategy, reduce regulatory bottlenecks, and ensure seamless distribution of investigational medicinal products.

Register now to gain expert guidance on accelerating your path to clinical success