TrialKit vs eResearch

TrialKit is a unified eClinical platform that connects sponsors, CROs, clinical sites, and study participants in a single secure environment. Whether you're completing study activities as a participant or managing clinical operations as a research professional, TrialKit delivers the tools needed to support modern clinical research from virtually anywhere. Participants can use TrialKit to complete electronic questionnaires, report symptoms, record diaries, attend scheduled virtual visits, receive study notifications, submit data from supported wearable devices, and stay connected with their research team using an intuitive mobile experience. Site staff and study teams can securely capture and review study data, manage participant activities, perform source documentation, monitor study progress, and support decentralized, hybrid, and site-based clinical trials through the same platform. Built on a unified cloud-based architecture, TrialKit brings together study design, participant engagement, data capture, analytics, and AI-assisted workflows without requiring disconnected systems. TrialKit supports: • Electronic data capture (EDC) • ePRO and eCOA • eConsent • eSource • eTMF • RTSM • Medical coding • Medical imaging (PACS) • Virtual visits and scheduling • Wearable device integrations via Apple Health • AI-assisted study design, build, validation, simulation, and analytics Researchers benefit from configurable workflows, role-based permissions, comprehensive audit trails, and real-time visibility throughout the study lifecycle. Participants benefit from a simple user experience that makes study participation more convenient while maintaining the privacy and security expected in regulated clinical research. TrialKit is trusted by sponsors, CROs, research institutions, and sites worldwide to support studies across a wide range of therapeutic areas and phases. Features available within the app may vary depending on your role in a clinical study and your organization's TrialKit configuration.

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