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A Successful Journey to Cell Therapy Manufacturing: From Research and Development to Lot-Release

A Successful Journey to Cell Therapy Manufacturing: From Research and Development to Lot-Release content piece image

Cell therapy is a transformative cancer treatment that utilizes genetically modified cells from a healthy donor or patient's own immune system to attack cancer cells, but manufacturing these cells represents a major challenge for the industry. Although every therapy and process are different, there are a few key decisions that are critical to the success of any advanced therapy medicinal product (ATMP) and for the success of the company that plans to bring them to the clinic.

In this webinar, we will discuss three main areas to consider when you're preparing to commercialize a cell therapy including starting/raw material, the controlled manufacturing process as well as testing safety and quality.

Watch now to learn about:

  • Regulatory requirements for GMP ancillary materials for cell and gene therapy
  • Closed-system manufacturing and how it can improve overall productivity and product safety
  • Characterization and lot release testing, proper validation for regulatory CMC filing
Speakers
Kasey Kime
Kasey Kime
Senior Manager, Regulatory Affairs
Sean Chang, PhD
Sean Chang, PhD
Manager, Early Innovation Cell and Gene Therapy