Jumar Masterclass: Clinical Trials Manufacturing Considerations

Manufacturing clinical trial material is one of the most complex and high-stakes stages of product development. This Masterclass explores how to plan, partner, and execute manufacturing for clinical trials — balancing cost, safety, and regulatory compliance.

Participants will gain practical insights into:

• Phase-appropriate GMP and what’s truly required at each stage.

• Choosing between in-house production or outsourcing to CDMOs 

• Managing risk, cost, quality, and legal obligations.

• Understanding key regulatory and supply chain considerations.

Masterclass Facilitator:

Rachel Jensen, Director at Centre for Biopharmaceutical Excellence

Speakers:

• Steve Williams, Director at Centre for Biopharmaceutical Excellence

• Justine Mann, CEO at CBE Pure Solutions
  

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The masterclass will be followed by an optional tour of Jumar Bioincubator. Let us know in the registration form if you're interested in participating.

NOTE: You may be photographed or videod while attending this event for marketing purposes: please approach the organiser if you have questions, concerns, or do not wish this to happen.

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About 

Jumar Bioincubator serves as a ‘first home’ for 30+ biotech ventures in Australia, providing affordable lab and office space alongside practical support to advance early scientific discoveries. Residents gain access to world-class facilities, a dedicated support team, and curated entrepreneurial training and events.

Established by CSL, WEHI and the University of Melbourne, and backed by Breakthrough Victoria with Cicada Innovations as operator, Jumar’s mission is to connect early-stage and scaling biotech ventures with the support needed to translate discoveries into real-world therapies and build a community of scientists equipped to lead successful biomedical ventures.