Advances in manufacturing technologies, as well as early development and adoption of industry-wide standards will contribute to a vibrant industry for cell-based therapeutic products (CTP). A critical aspect is manufacturing equipment that can address specific and unique challenges associated with CTP manufacturing. The move towards fully closed and automated systems heightens the need for integrated and standardized strategies to ensure the manufacturing of CTPs with controlled safety and quality profiles. This paper summarizes key points to consider for cell manufacturing equipment and components. In addition to enabling common baseline understanding for equipment requirements, it is meant to stimulate broader discussions for developing best practices and standards for CTP manufacturing equipment.