Cisiv_

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/p…

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

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

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

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

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_so…

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

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