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Market leading technology, dedicated to late phase and real world research

Offering tailored and flexible solutions that support the rich and diverse late phase landscape

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Intelligent technology for decentralized research, delivered by dedicated late phase experts, designed specifically for the unstructured nature of real world

One single platform, purposefully designed for late phase and real world research:

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    An intuitive platform, enabling study teams to capture, access and manage study data, without the need for multiple systems

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    Simple and clear user interface, which is easy to set up and easy to use

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    Industry-leading functionality, which engages physicians and patients alike, and the data associated with both

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    Delivers rapid study builds, improving operational efficiencies and delivering better data, faster

Building long lasting relationships with the biggest pharmaceutical and CRO's across the globe

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    Collaborating with
    of the top global
    pharmaceutical companies

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    Engaging with
    of the top global CROs

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    OVER 200
    studies delivered in the last 4 years

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    Proven to reduce data management costs by over

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    Delivering studies in more than
    in local languages

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    Supporting studies with less than 50 patients, to studies with over

Working with Cisiv

Our vision is to change the market, modify the way things are done and transform the sorts of results you can get from studies. It’s exciting, and our passion for challenging the way things are done to gain better results from these studies, is what really drives us as an organization.

Dominic Farmer

CEO and Founder, Cisiv

The study design team here at Cisiv play a vital role in ensuring end user engagement. The main role of Cisiv's study design team is to ensure that the design of studies are end-user centric. Ensuring the design is friendly and intuitive, encourages data entry from end users, helping to ensure more data, of better quality.

Megan O’Brien

Real World Study Design Manager

Cisiv is an organization established specifically to meet the needs of the late phase market. It is an ever-evolving organization with technology that is always one step ahead of the needs of this growing market. We pride ourselves in our expertise in helping our partners build their studies as efficiently as possible. Through our deep understanding of this industry, we provide access to skilled people, streamlined processes and tailored technology dedicated to creating the best solutions for late phase research.

Nadia Mahmood

Real World Studies Director

Baseline Plus supports eConsent, ePRO and eDiaries, meaning patients can submit their data either at home or on the go. That’s the unique thing about Baseline Plus – all of these modules are stored in the same platform, meaning that both patients and doctors are entering their data into the same database, making it much easier for review and analysis of data management.

Megan O'Brien

Real World Study Design Manager