Cell and Gene Therapy

Online
Cell and gene therapy represents a cutting-edge frontier in modern medicine, offering groundbreaking possibilities to treat and potentially cure a wide range of diseases. As the field continues to evolve and expand, the need for a well-trained and adaptable workforce remains critical to ensuring the successful development and delivery of these transformative therapies. This comprehensive course equips you with the scientific knowledge and hands-on skills essential for contributing to the manufacturing and development of cell and gene therapy products in both research and industrial settings.

Designed for individuals seeking to launch or advance careers in biomanufacturing, as well as professionals supporting clinical trials and research, the online course is self-paced and consists of four modules, providing a robust foundation in the principles, practices, and regulations that underpin cell and gene therapy production.

Here's what you'll cover:

Module 1: Introduction to Cell and Gene Therapy


Begin your journey with a broad overview of cell and gene therapies-what they are, how they are developed, and their transformative impact on healthcare. Explore real-world applications and gain insight into the perspectives of industry professionals currently working in the field.

Module 2: Cell Biology and Culture Techniques

Delve into the molecular workings of cells and the essential biological methods used to culture, maintain, and manipulate them in laboratory environments. Learn how these techniques are used to model biological systems and how cultured mammalian cells form the foundation for therapeutic development.

Module 3: Gene Therapy Concepts and Manufacturing Platforms

Examine the science and engineering behind gene therapy production, with a focus on AAV (Adeno-Associated Virus) platforms. Topics include therapeutic design, manufacturing workflows, quality control, regulatory pathways, and current industry challenges shaping the future of gene therapy.

Module 4: Stem Cells, GMP, and Regulatory Compliance

Explore the biology of human stem cells-including adult, embryonic, and induced pluripotent stem cells-and their use in regenerative therapies. Learn about CAR-T cell applications and gain a solid understanding of Good Manufacturing Practice (GMP) standards and the regulatory landscape governing the production of clinical-grade therapies.
Academic Units
0
Section Number
252CGT250
Instruction Method
Online class

Section Notes

Access to your course in Canvas will be available 7 days before the course start date.

Enrollment Policies

Refunds for this course must be requested within two weeks after the start date. The refund processing fee is $30. View complete enrollment policy information including details on withdrawals and transfers.

Refund Deadline: 10/6/25. Refunds and/or enrollment transfers will not be approved after this date.

Technical Requirements

Please review the technical requirements for participating in an online class: https://cpe.ucdavis.edu/areas-study/online-programs/technical-requirements