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REAL LIFE IS NOT A TRIAL

REAL LIFE IS NOT A TRIAL

Cisiv is a pioneer in technology for collating and curating real world data. We understand the sources of real world data and the best use of technology to collect data efficiently without adding to the burden of patients and healthcare practitioners.

Real world data is crucial to all phases of clinical development for both medicinal products and medical devices. Real world data provides effectiveness and safety information of an intervention in the real world. It can also help understand prevalence, incidence, natural history and disease patterns.

Get in touch to find out more about our platform and expertise

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

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

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

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

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

Cisiv provides the core technology for late phase research, which covers every aspect of data collection and analysis, and can be tailored to meet the needs of any real world, late phase study. Our Baseline Plus is a fully integrated platform with high flexibility, specifically built for the collection of real world data. It comprises of a single platform, with a complete set of tools and workflows that can be configured and customised.

Real world electronic data capture

At Cisiv our Baseline Plus technology is the only software that has been designed from the ground up for real world studies.

Patient centric solutions

Patient data can be used to demonstrate burden and understand treatment performance and safety, and so patient centric solutions are key.

eConsent

Informed consent is a pivotal aspect of late phase studies. Remote eConsent allows for the equivalent confirmation of paper consent to be achieved through the surrounding workflow a patient must go through.

Surveys

A survey is commonly used as a one-off cross sectional patient or physician survey. It can be utilised in market research to gain insight into the patient or physician experience during a study.

Expanded and managed access programmes

Real world data collection can be used alongside an expanded access programme to fill data gaps between clinical development and market access data requirements.

Latest Insights

Cisiv has completed projects for 40+ companies

abbvie
akebia
albireo
alexion
allergan
amicus
angelini
astrazeneca
alnylam
amgen
bayer
beigene
biohaven
biophytis
clovis
csl
deciphera
dompe
ferring
genentech
grail
gsk
hbharmony
immunocore
innova
janssen
jazz
lilly
mirum
msd
nrx
oncopeptides
orphazyme
rallybio
regeneron
rhythm
sanofi
sdbiosensor
servier
sobi
takeda
viela
viforpharma
stelmline
To learn more about our technology and how we can help you with your study, get in touch.
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  • 12th Floor CI Tower, St George’s Square, New Malden, KT3 4HG
  • +44 (0)20 8939 8470
  • info@cisiv.com
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