TrialKit - eClinical Platform vs eResearch Usage & Stats

Leverage the latest in data collection and study management technology to expedite clinical trials and advance healthcare. TrialKit eliminates the need for costly, outdated data collection tools by embracing the accessibility and efficiency of mobile operating systems. The mobility and versatility of TrialKit allow for seamless regulatory compliant (21 CFR Part 11) data capture from mobile devices anytime, anywhere. Once collected, data can be easily aggregated, analyzed and shared, making collaboration amongst research teams more productive. Best of all, no programming expertise is needed to use TrialKit, so any research professional can create a study using an iOS device. How does it work? 1. Build a study ​An intuitive user interface enables study builders to create electronic case report forms (eCRFs) to collect essential study data in accordance with the study protocol and regulatory requirements. Ensure accurate data collection with easy-to-create edit checks. 2. Collect data TrialKit enables research teams to collect and cleanse clinical data from virtually any location. Export data in a variety of formats for review and submission and capture ePRO data with ease. 3. Manage workflow With TrialKit, clinical research can be expertly managed from start to finish on an iPhone or iPad. Configuring role-based security, form review levels, and risk-based monitoring is simple. The ability to access, monitor, and review data or respond to queries on-the-go is now a reality. 4. Engage study participants The ePRO capabilities built into TrialKit will enhance your clinical trials. Automate the entire notification process and enforce patient survey completion by sending reminders. Study participants’ access has been made simple and flexible, so little or no training is required. Email and/or in-app notifications guide patients directly to their surveys, which can be accessed through the app or through any web browser. 5. Analyze data Robust reporting options enhance the ways research teams view and analyze data gathered in clinical trials. In addition to My Queries, Action Items, Regulatory Audit, and Outcome Summary reports, TrialKit generates a dynamic, visual report to track study progress in real-time. Unique Features and Functionality: Device-targeted eCRF design Image and video capture directly to eCRFs Site and study document support Built-in ePRO, including a patient handoff mode Adjudication for endpoints, outcomes, and inclusion/exclusion criteria Inventory management - Manage both drug and device inventory with a device you carry in your pocket. Barcode scanning eliminates human error and gives you real-time drug and or device disposition Harness the Power of iOS - Imagine uploading a photo, movie or voice narration to eCRF instantly and into the database. Program push notifications. Stamp GPS location to any record and view on a map. Operate in both landscape and portrait mode on any iOS device from an iPhone 5 on up. Sign case report forms with your finger or stylus. Activity Testing - Patients can now truly participate in their own treatments. Activity testing allows research professionals to measure a variety of different types of activity, using Core Motion and HealthKit. Drop range of motion, step motion, or heart rate tests directly into any visit interval within any study To learn more about this technology that allows the future of clinical trials to be possible today, visit https://www.crucialdatasolutions.com/.
  • Apple App Store
  • Free
  • Medical

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Join the eResearch community of clinical research volunteers to help end the addiction to cigarettes. eResearch is the first mobile clinical research platform that helps advance research in smoking cessation and harm reduction. Led by Dr. Jed Rose, co-inventor of the nicotine skin patch, Rose Research Center, LLC (RRC) enables at-home, remote participation in clinical research studies. By using eResearch you can participate in clinical trials which focus on researching nicotine addiction and smoking cessation. Today, the Surgeon General still lists cigarette smoking as the #1 leading preventable cause of death in the United States(1). At RRC we hope to make this statistic a thing of the past. Features Volunteer – We are seeking individuals, 21 years and older, that use nicotine containing products to volunteer by registering with the eResearch app. Simply provide your contact information and answer a few questions regarding your nicotine usage history. This information will help match you to current and future clinical studies. Participation – When matched with a study, eResearch allows you to enroll by providing your consent through our 100% online eConsent process. You can stop, or choose not to participate, at any time. Remember, your participation is always voluntary! Studies vary, and RRC offers new research studies all the time. As new studies launch, you can opt in for alerts to those in which you may be a good match. If I Participate, what does this app do? 1. Payments – Compensation is provided for study participation. eResearch utilizes an electronic payment gateway to pay you for your involvement. 2. Study Assessments – We may ask you to check in with us from time to time to see how you are feeling and progressing with the study. These assessments (also called remote visits) are scheduled in advance with our team of researchers. 3. Communication – Using eResearch, you can stay in touch with our study team. Our clinical research team will schedule appointments with participants throughout your participation in a study. Inside eResearch, Contact Us information includes phone numbers to reach study personnel and medical emergency phone numbers. 4. Telemedicine – Live telemedicine visits may be conducted through eResearch to engage with you just as if your study visit had been conducted in-person. Participants may meet with research or board-certified medical personnel, depending on the type of visit. Participant safety is our highest priority. Additionally, your volunteer information is kept confidential and is not shared with third parties. All research conducted by RRC is reviewed by an independent Institutional Review Board. Additionally, all studies are registered with clinicaltrials.gov and meet the requirements of Good Clinical Practice. (1) US Centers for Disease Control and Prevention. https://www.cdc.gov/tobacco/data_statistics/fact_sheets/fast_facts/index.htm
  • Apple App Store
  • Free
  • Medical

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TrialKit - eClinical Platform VS.
eResearch

December 17, 2024