Best Medical Quality Management Systems of 2024

RQM+, a global service provider for medical technology, is focused on accelerating market success and compliance. We deliver specialized solutions to medical technology companies and accelerate the journey along the entire product lifecycle, from concept through commercialization and post-market. Our portfolio of services allows us to deliver end-to-end products and solutions throughout the entire medical device lifecycle. RQM+ quality assurance engineers review materials lists, establish suppliers, and support design change processes. RQM+’s design quality engineers support any packaging, sterility or biocompatibility testing that may be required. RQM+ regulatory affairs consultants offer guidance and assistance with submissions to FDA, notified authorities, or other government agencies. Our extensive experience with the most recent reimbursement requirements and value based compensation models is what we use.

Batch records, cleaning and inventory management. Optimize advanced therapy with software that is designed for GMP. This is another way to align your team for 'right first time manufacturing'. {Get rid of fragmented paperwork with one software that everyone can use for data collection, review & approval workflows, reporting, and analytics.|With one software, everyone can access data collection, approval workflows, analytics, and reporting.} {Ensure your team follows the correct steps in due time to enable the right manufacturing with interactive work instructions.|Interactive work instructions will ensure that your team follows the right steps at the right time to enable the best manufacturing.} You can rest assured that the software is compliant with EU Vol 4 Annex 11 and 21 CFR Part 11. With bar code scanning, data integrity checks and automated calculations, you can easily log information. The software includes features such as highlighting out-of-specs and approval review. Know where your samples stand in the testing process. Organize your sample plans and automate trends. Know where your samples stand in the testing process. Track production processes and manage tasks to keep cleanrooms.

ZipQuality, a software-enabled medical device service, helps companies bring new products to the market. Our collaboration platform allows agile teams to make rapid design changes while maintaining regulatory compliance. System (processes and tool) pre-configured; no need to change your quality system. The integrated system is able to handle rapid design iterations in product documentation. Your team will be guided by experienced consultants at every stage. Software tools that are fully featured, scalable, and built on the powerful ENOVIA platform. Our integrated system allows for rapid design changes, while keeping data and documentation in sync. All records are maintained in a audit-ready condition. Product requirements, Hardware requirements, Software requirements. We have a deep understanding of complex, software-intensive devices. ZipQuality is a structured documentation system that supports good systems engineering and efficient risk management. It also provides clear traceability.

Defect-free business processes are the key to quality products. CASQ-it was designed to cover all aspects of your quality assurance and management processes, starting with the development phase and continuing through the material processing - including your support processes. The key advantage of CASQ is its process-oriented operation. This functionality allows your CAQ system adapt to your processes, and not vice versa. CASQ-it supports quality assurance processes as they move into the future. Quality and reliability increase customer satisfaction while reducing the cost per unit. Each CASQ-it module can be used independently, allowing you to optimize your individual processes and workflows in your company from the beginning. You can combine our modules to create a complete quality assurance system.

Regional Analyzer, the only Business Intelligence product on the market, allows you to evaluate your promotional investment on a regional basis. Evaluate the response of your promotional investment to the region. Compare the results and efforts in different zones and markets. Create a structured ranking based on the prescription market share of the area to evaluate. Periodic evaluations can be conducted by separating results at intervals that are customized. Integration solution that can be used without an Internet connection.

AmpleLogic's Quality Management Software is designed to meet the strict requirements of industries that are heavily regulated. The ISO 9001-certified cloud-based Quality Management System is ideal for Lifesciences and other industries such as Food & Beverages, Cosmetics, Medical Devices or Gene Therapy. Businesses are adopting QMS solutions as they recognize the challenges of manual quality checks, which can be laborious and prone to errors. These systems are crucial in improving audit quality by automating processes, managing data efficiently, and integrating APIs.

Momentum QMS is your guide in a world of uncertainty, complexity, ambiguity, and volatility. Momentum QMS is the best solution to your Quality, Safety, and Compliance needs. Momentum QMS's responsive design makes it easy to use from any device, for any function. Built-in reporting makes it easy to access the data you need, whenever and wherever you want. Momentum QMS is built on stable, reliable and widely-used Open Source software. Momentum QMS does not consume a lot of resources, and it leaves a very small footprint. No more silos. To increase enterprise-wide synergy, send and receive data from many sources. Multi-level authorization and role-based security allow you to keep your data and knowledge secure.

Cost-effective data capture. LifeSphere EDC offers sponsors and CROs an economical way to capture, manage, and report clinical research data. It combines disparate systems into one unified database, eliminating the need to reconcile and integrate them. The site captures clinical data directly, eliminating the need to enter data and fill out paper CRFs. Study development time is reduced and changes to live studies can be easily implemented. Integrate with the LifeSphere Clinical cloud platform – including LifeSphere eTMF, LifeSphere EDC – to seamlessly connect operations and data management. Single sign-on functionality allows easy access to a variety of applications. Open architecture allows for rapid integration with third-party applications via API.