Ratings and Reviews 0 Ratings
Ratings and Reviews 0 Ratings
Alternatives to Consider
-
Matrix RequirementsOptimize every phase of the development lifecycle with a versatile solution tailored for SxMD, allowing for effective management of design controls that span from initial requirements to compliance, all while ensuring comprehensive traceability to reduce risk. Accelerate innovation through a flexible item-based documentation strategy that caters to the intricate demands of even the most sophisticated SxMD products. Improve quality management by maintaining full traceability from design inputs to outputs with a specialized software platform that fosters collaborative quality practices across all departments. Take command of the shifting landscape of design, quality, and regulatory criteria while promoting team independence, ensuring your product reaches the market more swiftly. Achieve seamless integration across platforms with built-in connections to Jira, GitLab, GitHub, Azure DevOps, and more, while also utilizing our REST API to link all your essential tools effortlessly. This comprehensive approach empowers teams to not only adapt but thrive in a fast-paced development environment.
-
Lockbox LIMSA cloud-based Laboratory Information Management System (LIMS) is designed to oversee sample tracking, test outcomes, and inventory management specifically for life sciences research, industrial quality control laboratories, and biotechnology/next-generation sequencing applications. This comprehensive system provides essential regulatory compliance support for standards such as CLIA, HIPAA, Part 11, and ISO 17025, ensuring that laboratories operate within the necessary legal frameworks. The importance of quality, security, and traceability in managing samples cannot be overstated, as these factors play a pivotal role in a lab's effectiveness and reliability. Utilizing the Lockbox LIMS platform, laboratory professionals gain the ability to meticulously oversee their samples, offering complete transparency throughout the entire process, from initial accession to long-term preservation. Additionally, LIMS analysis encompasses far more than merely tracking outcomes; the Lockbox system features advanced multilayered sample storage capabilities and location management, allowing users to customize their laboratory's storage framework with diverse options that include rooms, storage units, shelves, racks, and boxes. This flexibility empowers labs to efficiently organize and access their samples, ultimately enhancing operational productivity and accuracy.
-
Nasdaq MetrioNasdaq Metrio serves as a sustainability reporting platform designed to assist businesses regardless of their progress in the ESG landscape. By integrating thorough data gathering, monitoring, and management with precise emissions assessments and verification, it creates a robust solution for sustainability reporting. Furthermore, it boasts an extensive repository of metrics sourced from multiple rating and ranking frameworks, along with regulatory organizations, ensuring that all information is cross-referenced, de-duplicated, and made clear, accompanied by helpful guidance notes for users. This makes it an invaluable tool for organizations aiming to enhance their sustainability practices and compliance efforts.
-
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.
-
Doc SheetsIntroducing Doc Sheets: Effortlessly Enhance Your Enterprise Lifecycle and Requirements Management Doc Sheets is an innovative and user-friendly software solution designed to streamline the complexities of enterprise lifecycle and requirements management. Its intuitive design, versatile features, and budget-friendly pricing allow organizations of all sizes to efficiently handle documentation and requirements throughout the entire product development process. Key Features: User-Friendly Interface: Designed for easy navigation, enabling both technical and non-technical users to minimize their learning curve. Requirements Tracking: Effectively capture, document, and prioritize requirements while ensuring traceability. Project Management: Efficiently plan and monitor tasks, milestones, and deliverables. Test Case Management: Create, categorize, and track test cases to guarantee comprehensive testing coverage. Lifecycle Management: Oversee the full development cycle from the initial planning phase all the way to product release. Customizable for Multiple Industries: Adapt the software to meet the specific needs of software development, embedded systems, medical devices, and beyond. Collaboration and Version Control: Facilitate real-time teamwork and maintain version control for better project outcomes. Cost-Effective Pricing: Offering budget-friendly options for organizations of any scale. Experience the benefits of Doc Sheets today and transform your management processes for the better!
-
AestheticsProAestheticsPro stands out as the leading all-in-one software solution for medical aesthetics in the current market. It boasts HIPAA compliance in the cloud, features integrated point-of-sale systems, targeted advertising, and comprehensive reporting that focuses on results, all while offering electronic charting and a client portal equipped with convenient "book now" options. With AestheticsPro, you have access to every tool necessary for effectively managing your medical spa operations. Whether you are looking to streamline appointments or enhance client engagement, this software has you covered.
-
Asym CapitalYou can reap significant rewards while minimizing the risks associated with market fluctuations. Our thorough evaluation methods and established partnerships are designed to assist you in managing your investment capital effectively. Gain entry to high-quality institutional opportunities spanning various asset classes. Engage in pre-screened transactions within the realm of private equity. Enjoy a steady stream of passive income deposited directly into your bank account. With our cutting-edge investor portal, you can monitor your investments with ease. Unlike typical crowdfunding platforms, we operate as a tech-driven investment firm focused on real estate. We commit our own capital to each offering, aligning our interests closely with yours, as our compensation is significantly tied to performance outcomes. This ensures that we are as invested in your success as you are.
-
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.
-
CredentialStreamCredentialStream® utilizes innovative patented technology to facilitate the requesting, collection, and verification of provider information, ultimately creating a trustworthy Source of Truth for subsequent processes. Its cutting-edge platform is regularly enhanced and is supported by extensive content libraries and top-tier data sets, making CredentialStream the premier solution for managing the entire lifecycle of providers. Additionally, the seamless integration of these resources ensures that organizations can maintain compliance and efficiency in their operations.
-
MLM SoftMLM Soft Cloud Platform (MLM Soft Cloud) offers a robust ERP solution tailored for MLM and Direct Selling businesses. Recognizing the urgency of launching your product or opportunity, we significantly expedite the process, enabling the deployment of MLM software within just a week. Our cloud-based platform is highly customizable, allowing you to modify everything from aesthetics to the content, accommodating various languages, currencies, wallets, user roles, notifications, and reporting features. Furthermore, our compensation plan engine is adaptable to any desired algorithm, providing flexibility in your business model. Designed to serve as the backbone of your MLM IT ecosystem, MLM Soft seamlessly integrates with various third-party applications, including e-commerce, CRM, payment systems, and marketing tools, all facilitated by its comprehensive REST API. This integration capability ensures that you can create a cohesive and efficient operational framework for your business.
What is RQM+?
RQM+ is a leading global player in the medical technology service sector, focused on helping its clients achieve compliance and market success more quickly. Drawing from extensive knowledge and industry experience, we provide customized solutions that enhance the entire product lifecycle for medical technology companies, guiding them from the initial concept to commercialization and further. Our broad range of services ensures a smooth, end-to-end experience that touches every phase of medical device development. The quality assurance engineers at RQM+ carefully assess material lists, build supplier networks, and aid in managing the design change process. In a similar vein, our design quality engineers focus on critical components such as packaging integrity, sterility assurance, biocompatibility, and necessary device testing procedures. Our regulatory affairs consultants are essential in delivering expert guidance and support with submissions to the FDA, notified bodies, and other regulatory agencies, ensuring that our clients navigate compliance effectively. Furthermore, we utilize our extensive knowledge of current reimbursement protocols and value-based compensation systems to bolster our clients' market positions. By working closely with medical technology companies, RQM+ is devoted to supporting them in achieving their objectives both efficiently and effectively, thereby enhancing their overall market presence. Our mission is to create a lasting impact in the medical technology landscape through our dedicated services and strategic partnerships.
What is LifeSphere Medical Affairs?
LifeSphere Medical Affairs, developed by ArisGlobal, is a cloud-based solution designed to enhance efficiency, ensure regulatory compliance, and foster collaboration among medical affairs professionals. It offers a unified workspace that merges medical information management with safety and quality assurance systems, facilitating thorough automation and real-time data sharing. This platform streamlines the process of collecting and managing medical inquiries across multiple channels, automates the processing of product complaints and adverse events, and ensures compliance with ever-evolving global regulatory standards. Equipped with advanced analytics and reporting features, it provides crucial insights that support data-driven decision-making and improve patient outcomes. LifeSphere Medical Affairs is tailored to be both scalable and customizable, catering to the unique needs of organizations of all sizes. Additionally, it enables medical teams to navigate effectively through a rapidly changing regulatory environment while enhancing their overall operational performance. This adaptability is particularly vital as the medical landscape continues to evolve, ensuring that teams remain responsive and proactive.
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
RQM+
Company Location
United States
Company Website
www.rqmplus.com
Company Facts
Organization Name
ArisGlobal
Date Founded
1987
Company Location
United States
Company Website
www.arisglobal.com/lifesphere/medical-affairs/