| nTruss is qualified to deal with a variety of client queries: - What are the requirements for FDA Phase I/II/III trials?
- How can my product be adapted to the FDA trial process?
- What is the difference between the clinical trial process for pharmaceuticals and devices?
- How can I run clinical trials in a country outside of the US?
- Is our product scientifically viable in the long run?
- It the efficacy / toxicity presented realistic?
- How can our product be expanded into additional products in the pipeline?
|
|