Regulatory bodies have provided recommendations for in vitro assays and to leverage high throughput screening technologies to increase the likelihood of rapidly moving therapeutic candidates into clinical trials.
This white paper discusses the requirements of regulatory bodies and how a rapid immunogenicity assessment screening can provide invaluable support for your application.
In this white paper you will learn:
For research use only. Not for use in diagnostic procedures.
ImmuSignature™ MLR: Rapid high-throughput assessment of therapeutic immunogenicity