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.
Days for of clinical trial authorizations
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