Site SOPs
Six standard operating procedures for investigator sites, each with dedicated templates. Designed to be implemented, not filed away.
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Clinical Trial Management
Site-level trial management from start-up to close-out, including delegation, readiness and enrolment tracking.
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Informed Consent Process
Procedures for obtaining, documenting and managing informed consent in compliance with GCP requirements.
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Investigational Product Management
Receipt, storage, dispensing and accountability of investigational products, including temperature monitoring.
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Biological Sample Management
Handling, storage and tracking of biological samples from collection through shipment.
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Safety Assessment and Reporting
Identification, assessment and reporting of adverse events and SAEs in line with regulatory requirements.
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Investigator Site File Management
Setup, maintenance, and archiving of the investigator site file, structured for audit readiness.
Expert Implementation Session
Two hours with an EUCRIT expert to go through the SOPs together. The expert explains, clarifies and answers questions, because reading a procedure and understanding how to implement it in your specific context are two different things.
The session is a conversation, not a presentation. You bring your questions, your doubts and the situations your team actually faces. The expert brings the experience to help you work through them.
Explore which EUCRIT plan includes SOP support.
SOP package and expert implementation support are included in the relevant site plan. Review the available plans to choose the level of access that fits your site’s needs.