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.
Augustus is a program that predicts genes in eukaryotic genomic sequences.
Enhance Your Clinical Trial Setup and Documentation Procedures with Agatha’s Electronic ISF - Simplify site & study configuration with our eISF Craft separate, protected areas for each Site to handle its documents. Each site and study incorporates a complete set of placeholders for expected eISF documents. Apply configurable auto naming to maintain naming conventions adhering to trial standards and facilitate compliant document management. - Dashboard access: Efficient workspace & tas
Provides clinical accruals
Auxilius is a cloud-based Clinical Trial Financial Management platform designed specifically for biopharmaceutical companies. It streamlines the financial management of clinical trials by integrating real-time clinical data, invoices, vendor estimates, and team inputs to provide accurate expense estimates. By replacing manual, spreadsheet-based processes, Auxilius enhances efficiency, reduces errors, and offers a single source of truth for R&D financials. Key Features and Functionality: -
The world's first degenerate sequence alignment algorithm, uncovering hidden "trillion-scale sequences" in patents Powered by world's first algorithm Accompanied by a database of 45 million degenerate sequences Enables you to effortlessly search for sequences in patents containing operators and degenerate symbols Mitigating the risk of overlooking sequences and potential freedom-to-operate (FTO) issues.
Digital pathology slides viewer powered by constantly improving state-of-the-art AI algorithms*
AmpleLogic's Cleaning Validation Software (CVS is a comprehensive solution designed to optimize and automate cleaning validation processes within the life sciences, pharmaceutical, and biopharmaceutical industries. By leveraging predictive analytics and real-time monitoring, CVS ensures that cleaning procedures meet stringent regulatory standards, thereby safeguarding product quality and patient safety. The software facilitates efficient resource allocation, enhances process efficiency, and prov
AmpleLogic's Process Validation Software is a comprehensive solution designed to assist regulated industries—such as life sciences, food and beverages, cosmetics, gene therapy, and medical devices—in validating and monitoring their manufacturing processes. By ensuring that these processes consistently produce products meeting predetermined quality standards and regulatory requirements, the software enhances operational efficiency and compliance. Key Features and Functionality: - Protocol Mana
DrugDev’s Solution integrates all of your investigator and site information to deliver a single, unified source that can be leveraged in master data management as well as in support of study planning, site identification, and site qualification.
Nested Knowledge is an AI-augmented platform for completing 'living' systematic reviews and meta-analyses. The software enables flexible Search/Import, Screening, Tagging, and Extraction features, and each step has AI assistance and automatically-generated visual outputs. Nested Knowledge reviews are collaborative, updatable, and shareable, and can support a range of uses, from publication to regulatory reviews to health economics and outcomes research projects. Beyond academic publishing, Nes
A Quality Management System (QMS) is a set of integrated processes, procedures, and tools that help organizations ensure the consistent delivery of high-quality products and services. It provides a structured approach to managing quality objectives, tracking compliance, and driving continuous improvement across operations. Ensure compliance with industry standards (e.g., ISO 9001)
Certivo is an FDA 21 CFR Part 11 compliant electronic signature platform built for clinical research, pharmaceuticals, and regulated industries. It provides ALCOA+ audit trails, two-factor authentication, 25-year document retention, and regulatory export tools for FDA, EMA, and MHRA inspections. Certivo supports EU CTR 536/2014, GDPR, HIPAA, and GxP compliance out of the box.
A bioinformatics data analysis AI agent
The annual product quality review (APQR) process is a requirement for manufacturers of drug products to comply with Good Manufacturing Practice (GMP) regulations and maintain high-quality products. However, data aggregation tasks and siloed analysis can plague APQR preparation often hindering product quality decisions, leading to inefficiencies and errors in the process. Streamline the creation of APQR reports with the Honeywell Product Quality Review (HPQR) app. Say goodbye to burdensome manu
The compliant cloud solution for content management for Life Sciences Companies.