Developing and supporting your nonclinical strategy

Across the life cycle of your development program, the right nonclinical studies at the right time are key to enabling your clinical development program and move it forward through each phase of development. We have the experts and the experience to design your nonclinical strategy and efficiently execute your nonclinical plan to keep your overall development on track.

Working with our network of strategic partners and service providers, Rho’s Regulatory and Product Development experts have supported many nonclinical development programs, including development of nonclinical program strategies and management of nonclinical testing programs, for pharmaceutical and biotechnology products.

We provide the following nonclinical services:

• Gap analysis and nonclinical strategy development
• Project management and support for CRO selection and management
• Study design and execution, including protocol and report development
• Regulatory authoring of nonclinical components of dossiers