What is myClin?
myClin enhances document management and collaboration with its innovative eTMF solution, making it a vital tool for research teams. Users can easily upload and distribute research documents via secure, centralized channels, ensuring that vital study updates and training materials are accessible without delay. The integrated oversight feature, "File it," enables tracking of who has reviewed and understood the study documents, serving as a reliable record of study execution while also monitoring training activities such as views and downloads at both the team and individual levels. Additionally, to ensure readiness for inspections, our compliance score provides insights into the engagement of each site or study team member with crucial study information, helping identify areas needing improvement. This proactive method not only enhances risk management practices but also promotes continuous development. Setting up a myClin channel for your team can be completed in just a few hours, ensuring a smooth experience from the outset. Discover how myClin can transform your study management processes and bring unparalleled efficiency to your team today.
Pricing
Free Trial Offered?:
Yes
Integrations
No integrations listed.
Similar Software to myClin
Castor EDC
Castor is an innovative clinical trial platform designed to simplify data management through electronic data capture (EDC), eConsent, and patient-reported outcomes (ePRO). Its flexible and user-friendly interface allows researchers to collect, manage, and analyze clinical data efficiently across multiple sites and remote patients. Castor’s tools are specifically designed to support decentralized clinical trials (DCTs), enabling real-time data monitoring, remote recruitment, and seamless patient engagement. The platform ensures full regulatory compliance, including HIPAA, GDPR, and 21 CFR Part 11, and is certified for ISO standards. With more than 50,000 global users, Castor continues to improve the speed and quality of clinical trials through integrated, scalable solutions that reduce administrative burdens and accelerate research.
Learn more
IQVIA
Across the globe, various organizations turn to IQVIA to expedite the drug development journey, ensuring product safety and quality while improving commercial effectiveness, facilitating appropriate treatment access for patients, and ultimately driving better health outcomes through enhanced healthcare delivery. By adopting a modern approach to clinical development that incorporates data, technology, and analytics, you can streamline your trials effectively. The result? Faster decision-making processes and reduced risks, allowing for the faster introduction of groundbreaking therapies. Leveraging its deep industry expertise, extensive data, and advanced analytics, IQVIA provides customized solutions to a diverse range of clients within the healthcare sector. You can keep up with the latest findings and updates shared by IQVIA's experts, including data scientists, healthcare professionals, and researchers, on significant topics that align with your interests. From trending industry shifts to practical applications of innovative capabilities, a treasure trove of knowledge is available for your exploration. Engaging with this rich content not only keeps you informed but also equips you to navigate successfully in an ever-changing healthcare landscape, ensuring you are always one step ahead.
Learn more
LifeSphere CTMS
Discover unparalleled oversight and seamless management with LifeSphere CTMS, an intuitive solution designed specifically for clinical operations teams aiming to boost productivity, stay organized, and streamline procedures. This contemporary cloud-based application focuses on reducing study timelines by optimizing management and automating crucial tasks throughout the clinical trial life cycle. Navigate the complexities of clinical research effortlessly with this powerful trial management tool, which provides complete visibility into all trial activities, ensuring that study teams remain aligned and on schedule. Transform your clinical operations using this comprehensive platform, which integrates payment processing and monitoring, while also guaranteeing smooth connectivity with LifeSphere eTMF. Furthermore, achieve adherence to the TMF Reference Model Exchange Mechanism Standard, which allows for easy document sharing across multiple platforms, thereby enhancing your clinical workflows even more. With LifeSphere CTMS, you can take your clinical trial management to unprecedented levels of efficiency and teamwork, ultimately driving better outcomes for research initiatives. This solution not only simplifies the management process but also empowers teams to focus more on advancing clinical research objectives.
Learn more
ClinAccess
ClinAccess™ 5.1 marks a significant advancement in our leading Clinical Data Management System, which is entirely constructed on the powerful SAS® 9 framework. This cutting-edge system enhances the efficiency of clinical data management, streamlines the analysis of clinical trials, and simplifies the preparation of electronic submissions. By allowing data entry to be performed directly into SAS® data sets, it eliminates the tedious task of transferring data from Oracle/SQL to SAS, greatly increasing your team's productivity. ClinAccess™ is designed with user-friendly features for study definitions, data entry, and management, including tools that monitor the progress and quality of ongoing clinical trials. Your data remains consistently organized within SAS® for straightforward access, whether it’s for review, analysis, or submission to regulatory bodies like the FDA. The database architecture is finely tuned to enable swift statistical analysis and reporting, ensuring users experience a significant reduction in the time and effort needed for data analysis, which can accelerate the overall time to market. Furthermore, ClinAccess™ is distinguished by its reliability, extensive auditing functionalities, and strong security protocols, making it an exceptional option for managing clinical data. With ClinAccess™, you can adeptly handle the intricacies of clinical trials while upholding data integrity and compliance standards, thereby ensuring the success of your research endeavors. This comprehensive system empowers organizations to achieve milestones with confidence in their data management processes.
Learn more
Screenshots and Video
Company Facts
Company Name:
myClin
Date Founded:
2008
Company Location:
United States
Company Website:
myclin.com
Product Details
Deployment
SaaS
Training Options
Documentation Hub
Online Training
Webinars
On-Site Training
Support
Standard Support
Product Details
Target Company Sizes
Individual
1-10
11-50
51-200
201-500
501-1000
1001-5000
5001-10000
10001+
Target Organization Types
Mid Size Business
Small Business
Enterprise
Freelance
Nonprofit
Government
Startup
Supported Languages
English
myClin Categories and Features
Clinical Trial Management Software
21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning