Manage and standardize all the visit activities

Manage and standardize all the visit activities and requirements, such as drafting agendas, completing visit logs, and providing a checklist of all activities that need to be accomplished during the visit.
Visit - Monitor and audit sites with ease. Provide checklist during clinical trial visit. Draft agendas, generate visit logs. Built-in travel policies.


Visit templates

Create visit templates that structure the way you want to execute a visit. add timeline, meeting, checklist, forms and make sure everything is up to date

Built-in travel policies

Create a policy that everyone follows by building it into visit duties. Watch as your compliance rates soar.

Monitor and audit sites with ease

Reduce the complexity of running site visits including Pre-study qualification visit,m initiation visit, monitoring visit and close-out visit.

Supercharge your team

An SIV or Site Initiation Visit is a monitoring visit that takes place after the Site Selection Visit. It is a visit that happens after the study sponsor has already selected the site for participating in a clinical trial.

Organize every detail of the visit

Make sure you have check all the dots before you get there.

Enforce compliance and regulation

Enforce industry best practices in every visit to improve outcomes. See critical information ( history, equipment, and more) during the visit.

Peace of mind

From ICH/GCP and 21 CFR to GDPR and HIPAA, we provide you the tools to focus on the trial with complete.

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Part of the Zapclinica platform

Zapclinica helps you managing your clinical trial, reduces the time to market, the cost, and the burden to run a successful clinical trial by operationally streamlining every task in an all-in-one platform.

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