Best Scientific Data Management System (SDMS) Apps for Android

SciNote is a cloud-based electronic lab notebook (ELN) with built-in inventory, compliance, & team management tools. It is trusted by the FDA, USDA, European Commission, and 100K+ scientists in over 100 countries. Each premium plan comes with top-rated customer support, and a customer success manager who will work closely with you to ensure successful onboarding and implementation. SciNote provides a top-rated set of data management functionalities, such as inventory tracking & management, protocol & SOP management, compliance (CFR 21 part 11 & GxP), team management & collaboration, integrations and API, project management, safety & security of data and more. SciNote is based in Middleton, WI, USA, with offices in Europe.

Compliance & CE is MediaLab’s all-inclusive course library and learning management system. This solution provides your employees or students with over 148 courses covering all major laboratory disciplines and ranging from basic to advanced. You can target all of your training needs with CourseBuilder, our included functionality that allows you to customize our courses and build your own courses. You can easily assign courses to specific groups of employees or students and track and review their performance. 10-15 new courses are added every year and automatically included in your subscription. Compliance & CE supports: • The CAP GEN.54200 requirement for an all-inclusive learning management system, • Course customization for targeted training, • Mass group assignments to employees or students, • Detailed score reports, dashboards, and automatic notifications to monitor performance, and more!

Seamlessly collect and combine a variety of data within a unified software platform. The integration of electromyography, force, pressure, motion, and high-speed video is complemented by automatic synchronization, creating a smarter workflow and reliable data. Collection, review, analysis, and reporting is now a streamlined process, even with data from many complex biomechanics recording systems. The myoRESEARCH® module configurations allow you to quickly select the devices to be used for your session and your data will be automatically time-synchronized. Customize your myoRESEARCH software to support any combination of Noraxon modules to fit your specific measurement needs. We now offer an analysis-only version of our software for free to current MR3 users. Whether you need to further your education, practice your techniques or simply want to process data outside the lab, we have you covered!

MediaLab’s Document Control is a powerful way to manage your laboratory’s policies, procedures, and documentation. Our twenty years of expertise in clinical laboratories have created a document control solution that guides you to full compliance with all laboratory standards, regulations, and best practices. Document Control provides an automated, centralized platform for all of your document approvals, workflows, edits, sign-offs, audits, and more—with flexibility and customization features to match your laboratory’s unique needs. MediaLab's Document Control supports: • Digital records and version control of all documents, • Standardization across all documents from all sites, • Electronic signatures that meet 21 CFR Part 11 standards, • Customized approval workflows and processes, • Robust searching to easily locate specific documents, and more!

We simplify the complexity of your entire product lifecycle management process. Easy-to-use and adaptable to your organization’s needs, the STARLIMS brand of lab informatics solutions support the rapidly changing data management needs across your organization. Our laboratory information management solutions (LIMS software) can integrate with your current systems, while also identifying opportunities to improve processes so you can bring high quality and safe products to market faster.

GoVal is a paperless validation lifecycle platform for regulated industries like pharma and biotech. It supports IQ/OQ/PQ protocols, full document control, audit-ready trails, and compliance with FDA 21 CFR Part 11 and EU Annex 11. Role-based workflows and e-signatures streamline approvals. Dedicated risk assessment tools help evaluate change impacts and ensure regulatory alignment. Integration-ready via APIs, GoVal connects with ERP/LIMS systems securely. Real-time dashboards, alerts, and GoVal AI enhance efficiency by automating risk analysis, test case creation, and document drafting—unlocking intelligent automation with tangible impact. GoVal lowers manual validation overhead, speeds up audit preparation, and shortens product validation cycles—helping organizations realize ROI quickly.