Starwriter - CLINICAL RESEARCH STUDIES
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Starwriter - The leader in Remote Clinical Research Studies
Enjoy confidence in:
End-to-end, fully Remote Clinical Research Studies
Real-time streaming access to data results- No waiting or delays
100% complete, structured data- no concerns with missing or poor quality data
Starwriter can assist in every component of Clinical Research studies and work in close coordinated effort with your company/ teams and PI ( Principle Investigator) or Starwriter can completely manage your Clinical Research Studies, depending on your team's/ company's preference and comfort level.
Starwriter assists with and manages:
Patient Recruitment
Patient Qualification
Patient Enrollment
Patient Approval
Maintaining Enrollment
All Physician-patient encounter data. With Starwriter, our EMR is the EDC
Real-time Streaming all data to your company, PI and teams
Synthetic Control Arms
Adjustment to criteria- if necessary
Real-time Alerts of adverse events
Automated required forms, tabulations and documentation
Analytics and reviews can be performed by your internal teams, or Starwriter can manage analytics and review for you company - depending on your preference.
* New - mHealth/Personal Device data. Starwriter's offer extends beyond/ outside of EHR data- Starwriter can now track vitals, Blood sugar, ECG and sleep data with the assistance of our new strategic partner.
Tracking data from personal data devices/ wearables provides deeper insights and gives a
3D view of how products are effecting patients.
*New -Pill dispense. Starwriter now can more accurately track patient compliance with medication dosing regimens, with the assistance of our new strategic partner.
With Starwriter, quality and completeness are never an issue, as it is with most CROs/ other data sources. ( graph above/left)
Consequently, we eliminate all of the most common issues and challenges for clinical research study data listed in the graph shown above/right.
Complete Control of Study Design
Starwriter puts the researchers, trial teams and PIs ( Principle Investigators) in control of the study design/ determining desired parameters.
Issue of primary vs secondary data – with all other data collection companies – you get secondary data, however, with Starwriter, the researcher selects all desired parameters - it is getting primary data, which is more reliable and desirable.
With All other sources - you are getting secondary data and using secondary data for your analyses. With other sources, they may have some details/ variables you wish to evaluate, however some data details that might be most beneficial to your study will be absent/ missing – this ultimately weakens your study/ clinical trial. With the Starwriter patented system – you can select your desired design parameters, even after the fact and Starwriter will provide all the data elements you wish to include.
More Cost Effective- Using all of the automation that the Starwriter Patented process provides- we can bring your teams/ company much more efficient, higher quality clinical trials and we are consequently far more cost effective.
Doesn't it make sense to run far more efficient trials ? And, since we offer far more cost effective DCTs than the CROs you are probably currently using - with Starwriter, you can perform More trials on your extremely promising new drugs .
Contact us today for a demo and to discuss how Starwriter remote Clinical Research Studies can help your company with clinical research studies at lowest cost and risk to your company and sponsors.
Enjoy confidence in:
End-to-end, fully Remote Clinical Research Studies
Real-time streaming access to data results- No waiting or delays
100% complete, structured data- no concerns with missing or poor quality data
Starwriter can assist in every component of Clinical Research studies and work in close coordinated effort with your company/ teams and PI ( Principle Investigator) or Starwriter can completely manage your Clinical Research Studies, depending on your team's/ company's preference and comfort level.
Starwriter assists with and manages:
Patient Recruitment
Patient Qualification
Patient Enrollment
Patient Approval
Maintaining Enrollment
All Physician-patient encounter data. With Starwriter, our EMR is the EDC
Real-time Streaming all data to your company, PI and teams
Synthetic Control Arms
Adjustment to criteria- if necessary
Real-time Alerts of adverse events
Automated required forms, tabulations and documentation
Analytics and reviews can be performed by your internal teams, or Starwriter can manage analytics and review for you company - depending on your preference.
* New - mHealth/Personal Device data. Starwriter's offer extends beyond/ outside of EHR data- Starwriter can now track vitals, Blood sugar, ECG and sleep data with the assistance of our new strategic partner.
Tracking data from personal data devices/ wearables provides deeper insights and gives a
3D view of how products are effecting patients.
*New -Pill dispense. Starwriter now can more accurately track patient compliance with medication dosing regimens, with the assistance of our new strategic partner.
With Starwriter, quality and completeness are never an issue, as it is with most CROs/ other data sources. ( graph above/left)
Consequently, we eliminate all of the most common issues and challenges for clinical research study data listed in the graph shown above/right.
Complete Control of Study Design
Starwriter puts the researchers, trial teams and PIs ( Principle Investigators) in control of the study design/ determining desired parameters.
Issue of primary vs secondary data – with all other data collection companies – you get secondary data, however, with Starwriter, the researcher selects all desired parameters - it is getting primary data, which is more reliable and desirable.
With All other sources - you are getting secondary data and using secondary data for your analyses. With other sources, they may have some details/ variables you wish to evaluate, however some data details that might be most beneficial to your study will be absent/ missing – this ultimately weakens your study/ clinical trial. With the Starwriter patented system – you can select your desired design parameters, even after the fact and Starwriter will provide all the data elements you wish to include.
More Cost Effective- Using all of the automation that the Starwriter Patented process provides- we can bring your teams/ company much more efficient, higher quality clinical trials and we are consequently far more cost effective.
Doesn't it make sense to run far more efficient trials ? And, since we offer far more cost effective DCTs than the CROs you are probably currently using - with Starwriter, you can perform More trials on your extremely promising new drugs .
Contact us today for a demo and to discuss how Starwriter remote Clinical Research Studies can help your company with clinical research studies at lowest cost and risk to your company and sponsors.
OR, if more convenient- go directly to our calendar and book an appointment time that works for you