Brochure | March 21, 2024

Testing At WuXi Advanced Therapies

GettyImages-1214763114 Medical Research Scientist Working In Laboratory

The field of cell and gene therapies holds immense promise for treating a wide range of devastating diseases. However, ensuring the safety and efficacy of these novel therapies requires robust testing throughout the entire development process, from initial discovery to commercialization. WuXi Advanced Therapies emerges as a key partner in this endeavor, offering a comprehensive suite of integrated testing services designed to streamline development timelines and navigate the complexities inherent in cell and gene therapies.

Understanding the unique challenges associated with these therapies is paramount. The inherent variability of biological materials, coupled with the need for meticulous safety testing on small sample sizes, necessitates a highly specialized testing environment. WuXi Advanced Therapies addresses these challenges head-on with a distinguished track record, supporting over 1700 customers with biosafety testing that meets global regulatory requirements.

Their expertise extends far beyond biosafety testing. WuXi Advanced Therapies boasts a team of highly qualified scientists with extensive experience in assay development, viral clearance, and lot release testing. This ensures not only the safety of the final product but also the efficiency of the development process. Their newly constructed, state-of-the-art testing facility boasts a significant increase in capacity, allowing them to tackle even the most demanding testing programs with exceptional speed and accuracy.

For researchers embarking on the development of cell and gene therapies, WuXi Advanced Therapies offers a compelling value proposition. Their integrated testing solutions provide the expertise, capacity, and efficiency needed to navigate the complexities of this burgeoning field. Partnering with WuXi Advanced Therapies can significantly accelerate the development timeline, ultimately bringing the promise of cell and gene therapies to patients faster.

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