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ClinSite360

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About ClinSite360

ClinSite360 is a clinical trial management software platform from Prescriber360 that supports the management and oversight of clinical trials. It includes features such as site selection, patient recruitment, and data management so that researchers can efficiently run their clinical studies. The platform is designed to help simplify communication between stakeholders, ensuring that all parties are informed throughout the trial process. Additionally, ClinSite360 provides tools for regulatory compliance and monitoring, which are essential for maintaining industry standards. Key capabilities: site selection patient recruitment data management regulatory compliance monitoring Best for: clinical research organizations and pharmaceutical companies that need to manage and conduct clinical trials effectively.

ClinSite360 Details

Vendor
Prescriber360
Year Launched
Location
350 N. Innovation Drive, Suite 200, North Chicago, IL 60064
Deployment
Training Options
demo, account manager, community
Countries Served
All Countries
Languages
English, Spanish, French, German, Italian, Japanese, Chinese
Users
Principal Investigators, Clinical Research Coordinators, Data Managers, Site Monitors
Industries Served
Healthcare, pharmaceutical, biotechnology, contract research, medical device
Tags
Clinical Trial Management, ClinSite360, PHT, Clinical Research, Site Management, Electronic Data Capture, Data Management, Regulatory Compliance

ClinSite360's In-App Market Place

Does ClinSite360 have an in-app market place?

Yes

How many Mini-Apps in the marketplace?

14

Mini Apps

1. ePRO (electronic Patient-Reported Outcomes): Allows patients to submit their responses to questionnaire and surveys electronically

providing real-time data collection and analysis.

2. IRT (Interactive Response Technology): Enables randomization of patients

drug allocation

and dispensation based on pre-defined criteria

ensuring efficient and accurate management of clinical trials.

3. eConsent: Facilitates the electronic signing and documenting of informed consent forms by patients participating in clinical trials

streamlining the consent process and ensuring compliance with regulatory requirements.

4. Site Monitoring: Provides real-time monitoring of clinical trial sites

allowing study coordinators and monitors to track progress

submit reports

and ensure adherence to protocols.

5. eSource: Digitizes source data collection by allowing investigators to directly input data into the system

reducing the risk of transcription errors and enhancing data quality and integrity.

Pricing Options

Free trial
Free version
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Accepted Payment Currencies

USD ($), EUR (€), GBP (£), JPY (¥), CAD ($), AUD ($), CHF (CHF), CNY (¥), SEK (kr), NZD ($), KRW (₩), INR (₹), RUB (₽), ZAR (R), BRL (R$), SGD ($), HKD ($), NOK (kr), MXN ($), DKK (kr), PLN (zł), TRY (₺), ILS (₪), PHP (Php), MYR (RM), THB (฿), AED (د.إ), COP ($), CLP ($), IDR (Rp), SAR (﷼), TWD (NT$), ARS ($), KES (KSh)

Pros & Cons

  • Streamlines the management of clinical trials, making the process more efficient and organized
  • Provides real-time access to data and insights, helping researchers make informed decisions quickly
  • Improves collaboration among research team members by facilitating communication and sharing of information
  • Enhances compliance with regulatory requirements by automating documentation and tracking processes
  • Increases overall productivity and reduces the likelihood of errors through automation and centralized data management
  • Limited customization options for study protocols
  • Steep learning curve for new users
  • Lack of integration with other clinical trial management systems
  • Inconsistent customer support
  • Problems with data synchronization between multiple users
  • Slow loading times for large data sets

ClinSite360's Support Options

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