Neuroscios has over 30 years of experience in drug development and 15 years of experience in the conduct of clinical trials with a strong focus on neurodegenerative diseases. This experience might make the difference between success and failure of your clinical trial.

Starting with the protocol, Neuroscios team will provide you with the necessary ingredients to prevent failure due to wrong planning, the wrong choice of clinical sites and bad study management.

A strong team of specialist in regulatory affairs throughout Europe will submit your study to IRBs or competent authorities in the countries of your choice. Neuroscios offers experienced project managers, senior CRAs, CRAs and CTAs. All CRAs have a scientific background or are nurses.

Throughout the study the Neuroscios team will support your trial trough overtaking all necessary tasks like site management, drug management, monitoring, and vendor management and will help with patient recruitment.