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Archives: Agenda

Chairperson’s closing remarks

END OF CONFERENCE

Clinical trial supply in 2025: opportunities and threats

• Contract manufacturing trends: players, clients and latest contracts
• Catalyst calendar: opportunities for vendors in 2025
• Supply chain disruption and resilience
• Digital or die

Start-up pharma & biotech’s; Establishing a relationship, engaging with your supply chain and selecting the right partners for you

  • Identify key supply chain stages, from raw material sourcing to final product distribution
  • Conduct due diligence to assess supplier capabilities, reliability, and compliance with regulatory standards
  • Evaluate potential partners based on their expertise

Sharing strategies for effectively managing (Investigational Products) during the clinical trial

• Overcoming common events during clinical trial
• Exploring efficient strategies for risk management
• Partnering with specialized vendors experienced in handling Investigational products supply

Morning refreshments and networking

Streamlining the End-to-End pharmaceutical supply Chain: Enhancing efficiency and quality

  • Understanding the complexities and challenges of the end-to-end pharmaceutical supply chain, from manufacturing to patient delivery
  • Addressing regulatory requirements and compliance
  • How did we implement effective strategies to enhance the end-to-end pharmaceutical supply chain

Chairperson’s closing remarks

Registration and refreshments

Chairperson’s opening remarks

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