Atrium can provide indicators for many fields of activity: regulatory issues, finance, quality, sales, marketing,
Dive deeper into "Scribe" on G2 AI
Established in 2012, Life Science Translation is leading its way as a certified medical translation company in the clinical, pharmaceutical, and veterinary industries. Our interpreters and translators are linguists in an extensive range of disciplines, from medical research to veterinary science. From simple medical certificates to professional websites, we offer accurate translation solutions for everything.
Our Interactive Web Response Systems (IWRS) offers a full-fledged Randomization and Trial Supply Management, also called RTSM. ClinicalHawk IWRS with its rare features, plays a vital role in managing and tracking products throughout the clinical trial. ClinicalHawk IWRS has a very user-friendly interface flow that proves to be useful in all types of trials. ClinicalHawk IWRS and IP Supply Management Solution are easy to set up and use. Moreover, our Intuitive Interface allows users to set up Ran
Rules-based fragment prediction for mass spectrometry. Have more confidence in your compound IDs, learn about fragmentation mechanisms, and publish your results easily.
RetinAI Discovery CORE is a software solution designed to enhance your research analysis by providing you with access to AI for medical data and the ability to share, understand and navigate data in a secure and collaborative way. CORE benefits physicians and researchers by accelerating research analysis efficiently and at scale. The platform quantifies endpoints and biomarkers automatically to quickly define patient subgroups. In addition to AI, CORE offers users the ability to annotate images
Comprehensive molecular structure drawing and naming. Draw chemical structures and communicate your science.
Predict absorption, distribution, metabolism, and excretion (ADME) properties from chemical structure. This collection of high-quality calculations of pharmacokinetic properties supports high-throughput screening of libraries, provides insights into pharmacological effects, and can help assure that products are safe for human use.
Symmetryk is the field enablement tool MSLs will love. Supercharge your HCP interactions using Symmetryk's presentation suite. Drive the right content to the right MSLs, while ensuring proper versioning and traceability. With Symmetryk, your content flows from your MLR system, to your DAM, and directly to the Symmetryk App or Web Portal, for easy consumption. A new standard in compliance Symmetryk was built from the ground-up to meet the requirements of the life-sciences industry. Control who
Systech provides product authentication and traceability solutions to help our customers optimize processes, achieve compliance and combat supply chain threats. Built on decades of Systech experience as the leader in pharmaceutical serialization our comprehensive suite delivers accurate real-time insight, actionable product data and digital connectivity across the supply chain.
Characterize samples and identify unknown components. One software solution for identifying compounds, processing data, and sharing your knowledge.
Rules-based fragment prediction for mass spectrometry. Have more confidence in your compound IDs, learn about fragmentation mechanisms, and publish your results easily.
Store & Share Live Analytical Data from Any Technique and Data Format
Kalderos MDRP Discount Monitoring is a solution to help pharmaceutical manufacturers gain a clear view of MDRP drug discounts. Eliminate inaccurate data and break down data silos throughout the dispute process, all in one place. Handle disputes directly with each state and manage responses easily in one dashboard. Kalderos MDRP Discount Monitoring solution helps stop revenue leakage due to noncompliant claims and recover previously paid noncompliant discount to ensure manufacturers pay only what
Predict genotoxic & carcinogenic endpoints of impurities and degradants to meet ICH M7 guidelines. Impurity profiling Suite can be used as part of your ICH M7 workflow—to help prepare regulatory submissions and remain compliant.
Tool using AI for harmonisation of mental health research data
Quantify the risk of a clinical trial ending uninformatively by examining the trial protocol to identify areas of risk.