Cisiv_

Intelligent technology for late phase and real world research.

[Cisiv_ @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 ➡️ https://t.co/d7njxKYrRN

[Cisiv_ @Cisiv_]

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?

➡️ https://t.co/O4FzGjCKMZ

@DrugInfoAssn #RealWorld #LatePhase #ClinicalTrials #EDC #DIA2022 #ClinicalDevelopment #eCOA #ePRO

[Cisiv_ @Cisiv_]

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

[Cisiv_ @Cisiv_]

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. ➡️ https://t.co/83KwoTfuLV

Let's shape the future of health together.

#eCOA #ePRO @DrugInfoAssn

[Cisiv_ @Cisiv_]

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. ➡️https://t.co/83KwoTfuLV

#DIA2022 #ClinicalDevelopment #RealWorld #eCOA #ePRO

[Cisiv_ @Cisiv_]

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.
https://t.co/zdg7FzYalB

#DIA2022 #ClinicalDevelopment

[Cisiv_ @Cisiv_]

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 [email protected]. Click here to register for the event➡️ https://t.co/32elPPbFhV

[Cisiv_ @Cisiv_]

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➡️ https://t.co/5qkJ8mGuv7

[Cisiv_ @Cisiv_]

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 ➡️ https://t.co/wOBVyAFsJG

[Cisiv_ @Cisiv_]

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➡️ https://t.co/MHpQ2o1WTO

[Cisiv_ @Cisiv_]

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➡️ https://t.co/5qkJ8moTDz

[Cisiv_ @Cisiv_]

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➡️ https://t.co/jfhvi9U1AV

Or to book a meeting, email us at: [email protected]

[Cisiv_ @Cisiv_]

#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➡️ https://t.co/wOBVyAFsJG

#pharma

[Cisiv_ @Cisiv_]

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➡️ https://t.co/DlYLaSSor5

[Cisiv_ @Cisiv_]

Baseline Plus covers every aspect of data capture and analysis to allow our customers to deliver new and existing studies.

Request a proposal ➡️ https://t.co/pp060CMAzH

Or email: [email protected]

#latephase #clinicalstudies #realworldevidence #realworlddata

[Cisiv_ @Cisiv_]

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!

[Cisiv_ @Cisiv_]

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 ➡️ https://t.co/jfhvi9U1AV

[Cisiv_ @Cisiv_]

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 ➡️ https://t.co/pp060CMAzH

#CROs

[Cisiv_ @Cisiv_]

#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➡️ https://t.co/4K9hw0CR3p

#pharma #biotech

[Cisiv_ @Cisiv_]

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➡️ https://t.co/MHpQ2o1WTO

#pregnancyregistry