is a choice if you need advice on what kind of study planning and running for a given product of your portfolio. We are specialised in delivering support when it comes to designing a clinical trial whether observational or randomised starting from identifying scientific data gaps in the fields and for the product.

is aimed at rendering CRO services to biotech and pharmaceutical companies using our knowledge and experience in clinical development.

advice on the best regulatory strategy to implement to get approvals and minimise timelines of start-up period.

provides clinical development services across all clinical trial phases and therapeutic areas including feasibility assessments, ethics committee and regulatory submissions, data management, statistical analysis, medical monitoring, safety solutions, central lab services, report write-up to ICH requirements, project and vendor management.

has established strong clinical teams in Europe and Russia with deep local knowledge to deliver quality CRO services. We are partnered with key specialist hospital and research facilities giving NEA Clinical clients direct access to the most active and reputable KOLs, PIs and sites to facilitate study start-up and patient recruitment to deliver on clinical timelines.