Iuvo BioScience’s expert pharmaceutical consulting team specializes in providing critical input to companies on their preclinical programs to support the development of new pharmaceuticals and their submission to regulatory agencies worldwide. Our collaborative approach and deep understanding of both the science and the regulatory guidelines positions us to provide the best strategies that both accelerate timelines and reduce program risk. We provide a breadth of expertise with our decades of collective years of direct global pharmaceutical Industry experience and treat each project as our own.
Our pharmaceutical consulting services include:
- Preclinical development strategy planning
- Study design development
- Safety assessments
- Position papers
- Preparation of preclinical submission documents
- Manage IND/NDA/MAA preclinical programs
We also serve as representatives on client project teams or at meetings with regulatory agencies.