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What we do
What we do

Cisiv develops an integrated platform specifically designed for real-world late phase research.
Technical solutions

Real world electronic data capture

Patient centric solutions

eConsent

Surveys

Expanded and managed access programmes
Study types

Observational studies

Post approval safety studies (PASS)

Registries

Retrospective chart reviews
Who we work with
Who we work with

At Cisiv we work with a range of different research organisations and life science companies across the globe.

Biotech and pharma

Contract research organisations (CROs)

MedTech

Patient advocacy groups

Academia
About
About Cisiv

Cisiv is a pioneer in technology for collating and curating real world data.

Our team

Our values

Our history

Why Cisiv?
Learning Centre
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Author: scottp

Blogs

When should I speak to a Cisiv expert regarding RWD vs acquiring a retrospective dataset?

February 20, 2024

Blogs

How does Cisiv’s platform scale if I want to run a study in one country and then add more countries?

February 20, 2024

Blogs

How does Cisiv’s technology reduce the burden on site for healthcare professionals?

February 20, 2024

Blogs

How is Cisiv’s platform Baseline Plus different from other e-Clinical systems?

February 20, 2024

Blogs

What is Baseline Plus?

February 20, 2024

Blogs

How to choose the right vendor?

February 20, 2024

Case Studies

Case study: an ambispective study featuring retrospective chart review and prospective cross-sectional surveys

February 20, 2024

Blogs

How can Baseline Plus address your post marketing needs?

February 20, 2024

News

Cisiv secures investment to accelerate growth

We are thrilled to announce a joint investment from Abbey International Finance and Ryan Group Holdings. The investment will accelerate

February 19, 2024

Webinars

RWD and HTA – from guidelines to real-world impact

Recorded: December 11 2023 In recent years, we have witnessed the emergence of frameworks in support of the use of

January 12, 2024

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