In drug development, there is high pressure to increase the number, scope and speed of clinical trials. At the same time, regulatory authorities demand stricter control and reporting.
Outsourcing is a very efficient way of preparing for the changing demands by getting access to the best experts in clinical trial processes and IT applications as well as handling workload peaks. NNIT offers you access to our experts within:
We have special focus on:
- eClinical
- Clinical trial services
- Post-Marketing Study Services
- Clinical Data Warehouse (CDW)
- Trial supplies and IVRS
- eSafety
A solid foundation in the pharmaceutical industry
Established to serve the pharmaceutical industry, we understand the issues pharmaceutical companies face. We have in-depth knowledge of the IT platforms and applications used to support clinical trials.
Our experts can help you optimise processes and implement new IT systems, always complying with the latest regulations. We comply with all guidelines from FDA, EMEA and local ethics committees, as well as 21 CFR part 11.
