Intelligent technology for late phase and real world research.
Joined September 2021
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Technology enablement is critical for effective #EAPs to deliver ethical, compliant, and controlled mechanisms.
Learn how we delivered an effective workflow for one #CRO, whilst equipping them with the tools to roll out the #tech to similar programs ➡️ cisiv.com/case-studies/post-…
Just one day till #DIA2022. We can't wait to see you!
The agenda is jam-packed with inspiring sessions. Which are you most looking forward to?
➡️ diaglobal.org/en/flagship/di…
@DrugInfoAssn #RealWorld #LatePhase #ClinicalTrials #EDC #DIA2022 #ClinicalDevelopment #eCOA #ePRO
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Just five days to go till #DIA2022.
Who else will be there? Let us know!
Cassandra Adams & Pamela Vizanko hope to see you there – find them on booth 1013.
@DIA #RealWorld #LatePhase #ClinicalTrials #EDC #DIA2022 #ClinicalDevelopment #eCOA #ePRO
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Will we see you in Chicago for #DIA2022?
Visit @Cassandra at booth 1013, to see how Baseline Plus can support #RealWorld #LatePhase data capture in #ClinicalTrials. ➡️ calendly.com/cisiv-cadams
Let's shape the future of health together.
#eCOA #ePRO @DrugInfoAssn
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Will you be at the @DrugInfoAssn Global Annual Meeting in Chicago?
> Visit Cassandra & Pamela on booth 1013 and discover how a tech partnership with Cisiv can improve your #LatePhase #ClinicalTrials. ➡️calendly.com/cisiv-cadams
#DIA2022 #ClinicalDevelopment #RealWorld #eCOA #ePRO
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Cassandra Adams and Pamela Vizanko, will be attending the @DIA 2022 Global Annual Meeting and discussing global and local challenges in #realworld #latephase research.
> Register now and come and see us at booth 1013.
diaglobal.org/Flagship/DIA-2…
#DIA2022 #ClinicalDevelopment
In less than 10 DAYS our Vice President of Sales and Marketing Adam Martin will be attending the @eClinical_Sol #OCTEU 2022 event.
Contact Adam today by emailing him at info@cisiv.com. Click here to register for the event➡️ cisiv.com/events/?utm_source…
Meet Nadia, Director of Real World Studies.
Nadia has expertly designed and delivered systems for a wide range of studies. Skillfully helping clients, #CRO’s and #sponsors to design eCRF’s through our versatile Baseline Plus platform.
Learn about Nadia➡️ bit.ly/37KU22M
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Does your #datacapture system accommodate regional language variations?
We recognise delayed #data collection is inefficient for #CROs and #pharma companies - we've delivered studies in more than 25 COUNTRIES in local languages.
Learn more ➡️ bit.ly/2WReb1Q
1 DAY TO GO!
#SCOPEEurope we're coming for you!
Cisiv's team of late phase experts will be on-hand to show how our simple, user-friendly interface can overcome challenges in any #clinicalstudy.
Find out how our #technology can digitise your study➡️ bit.ly/3sq5XLv
Cisiv’s Real World Studies Director, Dr Nadia Mahmood, explains what drives her passion for education, technology, and research.
Our late phase expert, Nadia, shares the impact of Cisiv’s #technology on targeting patient needs.
Learn about Nadia➡️ bit.ly/37KU22M
Would you like to meet our late phase experts at @ScopeEurope?
Join us on 20-21 April to find out how our #latephase technology drives operational efficiencies.
Click here to register to meet us➡️ bit.ly/3D8Qva0
Or to book a meeting, email us at: info@cisiv.com
#CROs and #sponsors - do you require technology that can function remotely?
Our Baseline Plus platform is delivered by dedicated #latephase experts and has enhanced capabilities for #decentralized research.
Learn how we can support your study➡️ bit.ly/2WReb1Q
#pharma
Are you planning to run an expanded access programme or compassionate use programme?
As experts in late phase, we recognise how crucial it is to have a system that supports the fast set-up of #ExpandedAccessPrograms.
Read our #WhitePaper➡️ bit.ly/3q9KT9Z
Baseline Plus covers every aspect of data capture and analysis to allow our customers to deliver new and existing studies.
Request a proposal ➡️ bit.ly/3BqJFuD
Or email: info@cisiv.com
#latephase #clinicalstudies #realworldevidence #realworlddata
Congratulations to all the 2021 #CitelineAwards winners!
As 2021 #finalists in two categories, we recognise the importance of these awards in celebrating the great work done in this industry.
Thank you to @Citeline for putting on the #awards and we look forward to 2023!
Join us at #SCOPEEurope's 4th Annual Summit.
Our VP of Sales & Marketing, Adam Martin, and Business Development Manager, Belinda Wilson, will attend this event to share how Baseline Plus powers #DCTs in the late phase, real world landscape.
Register ➡️ bit.ly/3D8Qva0
We pride ourselves on our late phase expertise in helping our partners build studies efficiently.
Our passion for challenging the status-quo to gain better results from studies is what really drives us as an organisation.
Request a proposal ➡️ bit.ly/3BqJFuD
#CROs
#CROs and #sponsors - are you tired of having to use multiple systems for #datacapture, remote consent and analysis?
Do you wish there was a more cost-effective and time-efficient solution?
Get in touch to learn about Baseline Plus➡️ bit.ly/3H8kE9Y
#pharma #biotech
Do you require a pregnancy registry for your study?
We worked with a leading #CRO to provide them with our expertise in #realworld, #latephase studies.
Click here to find out how Baseline Plus accommodated a hybrid consent approach➡️ bit.ly/3sq5XLv
#pregnancyregistry