“Bio Elpida is certified by the French Health Authorities (ANSM) as a Pharmaceutical Company to manufacture Active Pharmaceutical Ingredients and Advanced Therapy Medicinal Product. Our team feels proud to support innovative cell therapy development with capacity and expertise for projects from proof-of-concept studies to the clinic. As demand continues to increase for GMP development and manufacturing support, we are looking to take the next step forward by integrating with a leading supplier to deepen our impact on the industry,” CEO of Bio Elpida, Julien Gillet-Daubin, commented. 

“There is an increased demand for higher quality raw materials for Cell & Gene Therapy Manufacturing with increased regulatory scrutiny. Across modalities, we see that using scalable technologies and products to develop reliable processes from the start is most effective way to achieve commercialization success,” said CEO of Polyplus, Mario Philips. “We will continue evolving the Polyplus portfolio of products and services with a scalable foundation, including GMP manufacturing capacity, to optimize upstream process economics for each customers’ unique process.”

Existing cell therapy and fill and finish CDMO services will continue to be offered and developed, while leveraging fill and finish capacity to support Polyplus growth and customer needs for GMP grade transfection reagents. A network of external fill and finish partners will also be maintained for full business continuity.