The start-up of a clinical trial is one of the most complex and regulated parts. Usually, during this initial period a high number of interested parts are involved, such as: Regulatory agencies, ethics committees, suppliers and sponsors.
This is why it is very important to have all the optimized resources and processes at our disposal, as well as an effective planning to be able to adhere strictly to the client’s deadlines.
In Experior, we offer personalized Start-up services to meet your needs and our flexibility allows us to provide them in any region of the world according to the established specifications. Our qualified staff with extensive experience in the submission of documentation to committees and agencies in Europe and our vast knowledge of the particularities of each site allow us to facilitate the start-up process smoothly and efficiently.
Studies
Contracts signed
Days for of clinical trial authorizations
Different countries
Do you want more information
about our services?
Experior continues evolving!
We completed the integration process in the NEUCA Capital Group.
From this moment…
• Experior CRO becomes
• Experior SMO becomes
We grow and consolidate without losing our essence.
We put at your service a new agile structure, a global coverage, an organizational
network and a parent company that gives us stability and strength to meet the
needs of commercial and non-commercial studies.
Welcome to a new era!
Because "the best way to predict the future is to build it," and that is where we are.