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Product Description

NutrifyGenie is the world's first AI-powered platform designed to revolutionize the nutraceutical industry by streamlining the development and commercialization of ethical dietary supplements. By integrating over 3.5 million data points, including supply chain information, ingredient databases, and regulatory guidelines across 11 countries, NutrifyGenie enables businesses to bring differentiated products to market in half the conventional time. Key Features and Functionality: - Rapid Product

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Product Description

TriPort is clinical trial portal for providing sites with training, documents, communications and other valuable resources that streamline communications and eliminate time consuming workflows. Currently used at 7,000+ study sites and empowering 30,000+ active users, the TriPort platform supports a wide array of study team functions with intuitive tools that enable more efficient trial execution.

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A participant centric clinical trial recruitment platform. Our focus is participant empowerment.

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SDTM is the ETL tool that extracts data from ODM files and transforms it into SDTM codelists via drag-and-drop mapping and intelligent wizards.

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Combine computational biophysics, non-linear modeling, statistical approaches to structural protein biochemistry and progressive AI to explore combinatorial mutagenesis landscapes of any protein, irrespective of its class and application.

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Network Oriented Research Assistant brings research directly to patients in their homes through telemedicine.

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Owkin is a French-American startup that uses AI and machine learning to augment medical and biology research. Its proprietary platform, Owkin Socrates, uses machine learning technology to integrate biomedical images, genomics and clinical data to discover biomarkers and mechanisms associated with diseases and treatment outcomes. The company develops scientific collaborations with top-tier medical institutions and partners with leading pharmaceutical companies. Owkin has developed a state-of-the-

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A single centralized system across the study/project portfolio will enable companies to have a single source of truth to utilize for systematic monitoring of portfolio, project and studies performance, risk and compliance policies across.

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Next Generation Sequencing based Variant Analysis PlatformSEQ automates data transfer and back-up, organizes your data, performs detailed bioinformatics analysis and lets you access these in several different formats from any device connected to the internet.

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StoryPulse is an EASY customer engagement tool for your salesforce. It helps salespeople easily engage with customers to visually deliver content and surveys and effortlessly gather customer data points for analytics and segmentation strategies.

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Trials.ai leverages Artificial Intelligence to help organizations manage clinical trials, better.

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Longboat's cloud-based site and patient engagement platform empowers clinical trial site staff and patients to do the right thing at the right time, from patient recruitment through to study closeout.

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Tech Observer has been supporting the Pharmaceuticals & Life Sciences Industry since 2005. Services range offer flexible solutions to our clients ranging from standalone service to end to end support for their needs.

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Questionnaire software developed for patient audio-computer assisted self-interviews (A-CASI), patient self-report, behavioral research, surveys, social work informatics, and clinical use.

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Client-server based medical loaner device logistics running in Fortune 500 medical companies since 2000. Purpose-built with a full range of features required to run any sized Loaner Department. Designed by Loaner Technicians and Managers to handle the complex nuances of Loaner Asset Scheduling and Material Handling.Schedule and hard-book loaner sets in seconds through user friendly screens.

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Comprehensive and secure randomization software for clinical trials run entirely on the Internet.

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A cloud base software solution developed to speed the startup of clinical trials to impact patient enrollment.

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Redefine clinical trial regulatory document and TMF management with an automated, customizable 21 CFR Part 11 compliant solution.

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A disruptive big data SaaS platform, that accelerates new drug launches,lowers clinical trial costs, and enables RBM.

Product Description

Help your Clinical Operations team continuously improve speed, efficiency and data quality across your portfolio of clinical trials