Locations and dates:

  • Monday 16th September, San Francisco, Hilton San Fran Airport Bayfront.
  • Tuesday 17th September, San Diego, Marriot La Jolla.
  • Thursday 19th September, Seattle, Pan Pacific.

Launching your valuable drug product can be a daunting process, especially if you are not familiar with the key milestone requirements that should be met at various time points in the MA submission process.

During these knowledge sharing workshops, our subject matter experts will guide you through the product launch timeline. Taking you from Phase 3 to commercial launch, we will share with you the key requirements and considerations to ensure your commercial launch is successful.

View agenda

Key objectives

  • Learn about the European regulatory framework and how this determines all your launch milestones.
  • Understand the importance of the Qualified Person (QP) and QP declarations.
  • Discover key EU packaging considerations.
  • Gain insights into managing a complex supply chain.
  • Learn about the key Serialisation readiness requirements when partnering with a CMO.
  • Identify the top operational considerations as you progress to commercialisation.

EU product launch timeline

Not only will our experts share their product launch knowledge and experience but they will be hosting specialist roundtable discussions to address your specific product launch queries.

These roundtable discussions will give you the opportunity to speak with our subject matter experts and ask them more specific questions relevant to your particular project.

Round table session 1

Regulatory & Quality
Operational & Packaging

Round table session 2

Supply Chain & Serialisation
Operational & Packaging

Please complete the form to register for an upcoming workshop, choosing one option from each round table session.