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Ratings and Reviews 0 Ratings
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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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Castor EDCCastor 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.
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RegDeskRegDesk stands out as the leading RIMS platform enhanced by AI, tailored specifically for Medical Device, Pharmaceutical, and IVD companies. • Our unique Regulatory Intelligence encompasses data from over 120 countries, all presented in a uniform format, and includes timely alerts regarding regulatory updates. • With our AI-driven Application Builder, regulatory affairs teams can efficiently create and submit global applications in a fraction of the usual time. • The Change Assessment feature enables RA teams to evaluate the implications of changes on current products and determine the necessary actions. • Our Distributor Collaboration tool facilitates smooth workflows for communication and document sharing with external partners. • The Standards Management function simplifies the process for RA teams to locate and oversee both international and country-specific standards. • Additionally, our Tracking & Reporting capability empowers teams to monitor regulatory initiatives worldwide, receive notifications for renewals, and quickly compile reports on key performance indicators. To learn more about our offerings, please explore our website.
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FrameworkLTCFrameworkLTC offers a comprehensive and adaptable platform that streamlines all manual processes, enabling LTC pharmacies to concentrate on their primary goal: enhancing patient well-being. By transitioning from manual operations to automation, businesses can grow while optimizing their profit margins. Tailoring services to meet the unique requirements of each facility can also enhance partnerships. Our software, designed with a facility-focused approach, empowers you to deliver exceptional service to every patient, section, and establishment. Facilities can easily manage billing, track order statuses, and handle returns based on your established protocols. Your facilities will find great value in the insightful reports you provide. Additionally, automate the prescription refill and reorder process to ensure nothing is overlooked during production. By leveraging this technology, you can significantly improve operational efficiency and patient satisfaction.
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LLuminLLumin's CMMS+ offers a robust software solution tailored for the effective management of assets, facilities, and maintenance tasks. This platform boasts an array of features that empower organizations to optimize their maintenance procedures, minimize downtime, and enhance overall productivity, all while achieving substantial savings in both time and expenditures. The advantages of using LLumin's CMMS+ are extensive. By refining maintenance processes, organizations can achieve lower downtime and heightened efficiency. Additionally, proactive asset maintenance helps avert expensive failures and prolongs the life of equipment. Automation of inventory control ensures that essential parts and supplies are readily available, further decreasing delays in maintenance work orders. Moreover, the provision of real-time data and analytics equips organizations with the insights necessary to make strategic decisions and enhance their maintenance strategies. Ultimately, the return on investment (ROI) associated with LLumin's CMMS+ is considerable; organizations can enjoy notable financial benefits through reduced downtime and improved operational efficiency. By focusing on asset longevity and preventive care, they can also dodge costly repairs, leading to lower overall maintenance expenditures. This software not only transforms maintenance practices but also promotes a culture of proactive asset management within organizations.
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OpenClinicaOpenClinica stands out as a prominent provider of software solutions for managing clinical data. Their robust tools are designed to enhance the compliance and efficiency of clinical trials. The main offerings from OpenClinica include OpenClinica Enterprise, OpenClinica Participate, and OpenClinica Randomize, which together facilitate a comprehensive approach to clinical data management. Each product addresses specific needs within the clinical research landscape, making them essential for successful trial execution. OpenClinica is an industry-leading platform that enables more efficient and effective clinical trials by providing a comprehensive range of tools for managing data, patient engagement, and recruitment. Key features include electronic data capture (EDC), patient-reported outcomes (ePRO), and fully automated eConsent, all designed to improve accuracy and streamline study workflows. The platform supports EHR-to-EDC integration, reducing manual errors and accelerating data collection. OpenClinica also offers robust reporting and data analysis tools, ensuring real-time insights into trial progress. With over 15,000 studies powered and more than three million patients involved, OpenClinica is trusted by life sciences organizations worldwide, from pharmaceutical companies to academic researchers and government bodies. Its seamless integration, user-friendly design, and comprehensive features make it an essential tool for advancing clinical research.
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SDS ManagerSDS Manager stands out as a leading provider of Safety Data Sheet (SDS) Management solutions, boasting one of the most extensive SDS databases globally, which contains over 14 million Safety Data Sheets available in 25 different languages. With SDS Manager, employees can conveniently retrieve crucial SDS information directly on their mobile devices by scanning QR code posters placed in areas where chemicals are handled, thereby enhancing both safety measures and adherence to regulatory standards. This intuitive mobile access not only facilitates immediate information retrieval but also fosters a culture of safety within the workplace. Additionally, our automated data extraction capabilities allow for the effortless integration of SDS files into your library without the need for manual data entry, which greatly enhances accuracy and optimizes the process of SDS management. Your SDS library remains consistently updated, well-organized, and readily accessible, all within a secure cloud environment, ensuring that you are always prepared for audits or emergencies.
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EldermarkEnhancing workflow processes, optimizing revenue, advancing business development and marketing, along with improving clinical outcomes, can be achieved effectively. By seamlessly connecting your entire community, you can empower your staff to enhance their performance while gaining a comprehensive overview of your community's financial health. This approach will equip you with proactive insights necessary for streamlining operations and maximizing revenue potential. Centralizing all clinical and business activities onto a single platform will provide you with simplified solutions, economies of scale, and heightened security, essential for delivering top-notch care. Furthermore, you'll gain deeper insights into your performance in relation to financial and occupancy targets, staff safety, and satisfaction levels, enabling you to address the numerous challenges you encounter daily. Ultimately, this integrated strategy will facilitate a more efficient and effective care environment.
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CGM LABDAQCreated by CompuGroup Medical, CGM LABDAQ stands out as the premier laboratory information system in the country. It features a contemporary, user-centric platform that leverages years of expertise in the LIS market. Using the reliable MS-SQL Server database, CGM LABDAQ enables laboratories of varying sizes to boost their revenue and enhance customer loyalty. By implementing CGM LABDAQ, your laboratory can improve its operational efficiency, streamline processes, ensure patient safety, and shorten turnaround times significantly. Designed to adapt alongside your evolving business requirements, CGM LABDAQ provides a range of modular software options, including LAB IQ, an interactive dashboard that allows users to monitor performance metrics in real-time. This feature eradicates manual workflows, thereby enhancing overall efficiency. Additionally, its interface monitoring tools provide alerts to ensure proper functionality, eliminating the necessity for daily quality control tasks. Beyond these capabilities, CGM LABDAQ also includes robust options for data analytics, workflow optimization, inventory management, and more. The system's advanced, rules-based technology not only aids in adhering to best practices but also facilitates the seamless and efficient operation of your laboratory. Furthermore, its continuous updates ensure that your lab remains at the forefront of innovation in laboratory management.
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Predict360Predict360, developed by 360factors, serves as a comprehensive risk and compliance management platform designed to streamline workflows and improve reporting for various financial institutions, including banks, credit unions, and insurance companies. This cloud-based SaaS solution consolidates essential components such as regulations, compliance management, risk assessments, controls, key risk indicators (KRIs), audits, policies, and training into one cohesive platform while offering powerful analytics and insights that help clients foresee risks and enhance compliance efforts. If your current Governance, Risk, and Compliance (GRC) system isn't equipped with an effective analytics and business intelligence tool for creating insightful reports for executives and board members, consider Lumify360 from 360factors. This predictive analytics platform can seamlessly integrate with any existing GRC, allowing you to maintain your workflow processes while equipping stakeholders with the timely reports and dashboards they require for informed decision-making. With these advanced tools at your disposal, you'll be better positioned to navigate the complexities of regulatory compliance and risk management.
What is PharmaPendium?
PharmaPendium is a comprehensive resource that provides users with access to a wide range of drug approval documents from the FDA and EMA, covering crucial elements such as pharmacokinetics, pharmacodynamics, and safety assessments. This platform offers valuable insights into drug interactions, adverse effects, and clinical trial outcomes, enabling stakeholders to make informed decisions in both drug development and regulatory submissions. Its extensive database supports researchers and healthcare professionals in evaluating the safety and effectiveness of various medications, thereby playing a critical role in advancing pharmaceutical research and improving patient care. Users can also investigate historical regulatory submissions and utilize previous cases to gain a clearer insight into agency expectations. The user-friendly interface facilitates an easy transition from raw data to engaging visual representations like charts and graphs, enhancing the analysis and interpretation of results. Furthermore, the platform allows users to search for information on adverse events (MedDRA), therapeutic targets, drug indications, and endpoints through standardized data. Result pages effectively link preclinical research with clinical applications, offering a holistic view of the drug development ecosystem. Overall, PharmaPendium not only simplifies the research process but also encourages collaboration and knowledge exchange among professionals in the industry, ultimately contributing to better health outcomes. The array of features offered by this platform makes it an invaluable tool for those involved in the pharmaceutical field.
What is Drug Safety Triager?
Clarivate's Drug Safety Triager is a sophisticated pharmacovigilance solution designed to assist life sciences organizations in meeting regulatory requirements effectively. This tool, which has been validated for Good Practice (GxP) compliance and is ready for audit processes, optimizes the workflow involved in literature reviews, enabling pharmacovigilance experts to focus on patient safety by refining these actions. Fully aligned with the reporting requirements of leading global safety regulatory authorities such as the FDA and EMA, the Drug Safety Triager is accompanied by a thorough validation package with each implementation. The validation documentation is meticulously crafted to satisfy the rigorous standards established by the pharmaceutical industry and health governing bodies. Moreover, every literature item included undergoes a detailed review, ensuring that all user interactions are meticulously documented, thus creating a permanent, unalterable audit trail that promotes accountability and transparency. This forward-thinking approach not only boosts operational efficiency but also reinforces the unwavering dedication to upholding high standards in patient safety and compliance with regulations. Ultimately, the Drug Safety Triager represents a pivotal advancement for organizations striving to enhance their pharmacovigilance practices while ensuring robust safety and regulatory adherence.
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
Elsevier
Date Founded
1880
Company Location
Netherlands
Company Website
www.elsevier.com/products/pharmapendium
Company Facts
Organization Name
Clarivate
Company Location
United Kingdom
Company Website
clarivate.com/life-sciences-healthcare/research-development/pharmacovigilance-drug-safety/drug-safety-triager/