All Phase I clinics face similar challenges: Lots of data, systems, assessments, changes, paper and spreadsheets. So how to keep focused on volunteer safety and study results?
Learn in one minute what ClinSpark is and how it can help solve your Phase I challenges.
ClinSpark is built from the ground up on the most modern technology standards.
However complex your Phase I unit, all systems and devices connect into ClinSpark, so you can access all study data in one place.
Because everyone is looking at the same data in real time, teams can work more closely together and get to better decisions faster.
ClinSpark is designed with Ease of Use in mind. Your staff will find it to work better and faster than conventional methodologies.
A unique set of features make ClinSpark the ideal platform for running Phase I trials.
Everybody working on a Phase I trial will benefit from using ClinSpark. The Sponsor will have in-depth 24/7 insight into study status. The Scientist will have extensive tools to review study results in real time. The Data Manager will enjoy very clean data to work with. But the biggest benefits occur in the clinic. Learn from these professionals how ClinSpark helps them in their daily tasks.
I enjoy using it for feasibilities and matching subjects to trials quickly. I now have always an up to date recruitment status.
ClinSpark gives me deep insight in volunteer safety. I can quickly review data and sign-off on lab results, eligibility and Adverse Events.
We have no paper sources anymore, fantastic! And staff is saving lots of time as everything they need for data collection is just a barcode scan away.
ClinSpark comes as a Software as a Service offering only. Its pricing is largely based on actual use. There are no long contractual commitments, you can cancel any month. Based on specific needs, there are three packages you can choose from.
If you would like to learn more about ClinSpark, please write us a short message and we will get back to you soon.
For support inquiries, please use our service desk for registered users. Otherwise please contact the study team at the CRO or sponsor organization responsible for the clinical trial.