Clinical and Regulatory Development Services
Scalable Consulting Services for Clinical R&D Program Planning and Management
Clients rely on ProSciento’s experience and expertise to optimize their clinical programs from strategy and study designs to conduct and analysis.
Our clinical and regulatory development services are tailored to the specific needs of our clients and typically begin with a well-defined target product profile and clinical development plan. Clients work with our team of seasoned professionals, comprised of PhD and MD level scientists, that have long-standing track records in metabolic drug development.
Examples of ProSciento’s Clinical Development and Regulatory Services:
- Target Product Profiles (TPPs)
- Clinical development planning
- Clinical study design and protocols
- Regulatory strategy and operations
- Medical writing and publishing, including scientific publications and presentations for clinical trial and NASH PASS programs