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IQVIAAcross 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.
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Jama ConnectJama Connect® is an innovative platform for product development that establishes Living Requirements™. It weaves together disparate activities related to testing and risk management, ensuring comprehensive compliance, mitigating potential risks, enhancing processes, and maintaining adherence to regulations. Organizations involved in developing intricate products, systems, and software can now effectively outline, synchronize, and implement their requirements. This streamlined approach significantly decreases the time and resources needed to demonstrate compliance and minimizes the need for rework. By selecting a user-friendly, adaptable solution accompanied by supportive services focused on fostering adoption, companies can confidently pave the way to their success. The platform’s design emphasizes collaboration, ensuring that all stakeholders are aligned throughout the product development lifecycle.
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InspectivityInspectivity enables the efficient planning, assignment, scheduling, and documentation of inspections for essential assets. Customized digital inspection reports, generated electronically, ensure a consistent inspection methodology while maintaining comprehensive audit trails of all actions taken. The guided process enhances both control and integrity, facilitating automation assessments and informed decision-making. Non-compliant assets can be quickly identified, and users have access to all necessary features for managing issues, implementing corrective measures, and tracking historical data. Additionally, non-compliances can be documented alongside annotated photographs, and users can make modifications to drawings while utilizing RFID and barcode technologies. Asset history and information are readily accessible on the go, allowing for quicker inspections through the collection of field data stored in the cloud for seamless desktop collaboration. Furthermore, the platform presents opportunities for cost savings and robust automation by integrating intelligent asset insights directly into the inspection process, ultimately streamlining operational efficiency. By leveraging these advanced tools, organizations can enhance their asset management strategies significantly.
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MedsenderMedsender offers a comprehensive automation solution for healthcare, featuring HIPAA-compliant faxing, emails, SMS, forms, and signatures, all effortlessly integrated into your electronic medical records (EMR) system. Utilizing cutting-edge artificial intelligence, it streamlines processes by securely managing incoming faxes through a cloud platform that sorts them automatically to the appropriate staff and patient charts. Patients benefit from an easy-to-use interface for filling out forms and sending notes, further enhancing communication and efficiency. With a simple one-click setup, there's no need for traditional fax machines, and Medsender's compatibility with all major EMRs, along with ongoing integration developments, ensures flexibility. Additionally, it can function independently of an EMR, allowing for versatile usage across various healthcare environments. By leveraging the latest AI advancements, we help you minimize repetitive tasks and unnecessary busy work, providing peace of mind. Currently, Medsender successfully handles over 5 million pages of patient data while maintaining an impressive uptime of over 99.9%. This commitment to reliability and efficiency makes Medsender an invaluable asset for healthcare providers seeking to enhance their operational workflows.
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KrakenDDesigned for optimal performance and effective resource management, KrakenD is capable of handling an impressive 70,000 requests per second with just a single instance. Its stateless architecture promotes effortless scalability, eliminating the challenges associated with database maintenance or node synchronization. When it comes to features, KrakenD excels as a versatile solution. It supports a variety of protocols and API specifications, providing detailed access control, data transformation, and caching options. An exceptional aspect of its functionality is the Backend For Frontend pattern, which harmonizes multiple API requests into a unified response, thereby enhancing the client experience. On the security side, KrakenD adheres to OWASP standards and is agnostic to data types, facilitating compliance with various regulations. Its user-friendly nature is bolstered by a declarative configuration and seamless integration with third-party tools. Furthermore, with its community-driven open-source edition and clear pricing structure, KrakenD stands out as the preferred API Gateway for enterprises that prioritize both performance and scalability without compromise, making it a vital asset in today's digital landscape.
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Adaptive Compliance Engine (ACE)The Adaptive Compliance Engine® (ACE®) is a versatile, workflow-driven eQMS/eDMS solution that can seamlessly adjust to various business processes, providing real-time oversight, management, and reporting for compliance, quality, and operational tasks. By utilizing ACE®, organizations can alleviate administrative burdens and enhance ROI through immediate productivity improvements, while maintaining adherence to 21 CFR Part 11 regulations. Our comprehensive software suite features: -Office 365 Integration -Inspection Management -Document Management -Risk Management -Product Lifecycle Management -Learning Management -Audit Management -Quality Events -Paperless Validation -Electronic Signatures (21 CFR Part 11 Compliant) -Endless Workflow Configurations -And numerous additional capabilities! Enable every tier of your organization with user-friendly interfaces, effortlessly locate all documents and records, and convert your data into insightful intelligence through advanced analytics, all within one unified platform. Every essential application is bundled together at a single price with ACE, eliminating the need for separate purchases. Enjoy the convenience of one software solution with countless functionalities, making it a truly invaluable asset for your business.
What is TrialPoint?
TrialPoint™ electronic data capture (EDC) system stands out for its exceptional adaptability and ease of use, earning the trust of coordinators across the board. Our expert data managers are dedicated to converting clinical protocols into user-friendly metadata dictionaries, ensuring that TrialPoint™ is customized to meet your specific needs instead of complicating your workflows. The platform is designed to support any randomization string, media uploads, or coding dictionaries, and it includes features that allow for the concealment of treatment assignments from users. To promote efficient data collection, the system intelligently identifies visit windows and sends out alerts and reminders, which aids in keeping the whole team synchronized and focused. In today’s environment, integrating patient-reported health outcomes and quality of life assessments into clinical trials has become standard, often resulting in challenges with protocol adherence. Discover the ePRO module offered by TrialPoint, which can be tailored to fit any quality of life questionnaire or patient diary, ensuring a smooth experience for participants. This remarkable flexibility not only boosts compliance but also improves the overall integrity and quality of the data gathered in clinical research. By utilizing TrialPoint™, you can streamline your trial processes and enhance participant engagement significantly.
What is Clinical Research IO?
Discover the leading edge of eSource, CTMS, and eRegulatory software tailored for clinical trial sites with CRIO. Our premier electronic source enables you to capture source data in real-time, significantly reducing paper dependency by up to 90% and improving data quality by 80%. Take control of your operations with CRIO’s intuitive Clinical Trial Management System, which streamlines patient scheduling, financial oversight, and recruitment optimization. We proudly offer innovative electronic regulatory binders, featuring the groundbreaking first-ever electronic delegation log, all fully compliant with 21 CFR Part 11 regulations. For sponsors of clinical trials, our secure online portal allows for complete remote monitoring of your sites’ source data and regulatory documents. Join our vast network of over 500 clinical research sites globally, and benefit from our dedication to enhancing your business by simplifying your site operations. This ensures that your studies progress seamlessly, whether you are on-site or working remotely, allowing you to concentrate on what truly matters: propelling your clinical research efforts forward while ensuring efficiency and accuracy throughout the process.
Integrations Supported
Additional information not provided
Integrations Supported
Additional information not provided
API Availability
Has API
API Availability
Has API
Pricing Information
Pricing not provided.
Free Trial Offered?
Free Version
Pricing Information
Pricing not provided.
Free Trial Offered?
Free Version
Supported Platforms
SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux
Supported Platforms
SaaS
Android
iPhone
iPad
Windows
Mac
On-Prem
Chromebook
Linux
Customer Service / Support
Standard Support
24 Hour Support
Web-Based Support
Customer Service / Support
Standard Support
24 Hour Support
Web-Based Support
Training Options
Documentation Hub
Webinars
Online Training
On-Site Training
Training Options
Documentation Hub
Webinars
Online Training
On-Site Training
Company Facts
Organization Name
Databean
Date Founded
2007
Company Location
United States
Company Website
databean.com/trialpoint/
Company Facts
Organization Name
Clinical Research IO
Date Founded
2015
Company Location
United States
Company Website
www.clinicalresearch.io
Categories and Features
Clinical Trial Management
21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning
Categories and Features
Clinical Trial Management
21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning