Best Life Sciences Software in the UK - Page 7

So much more than a repository for names and addresses. Generating awareness about who has received your message and how, it can be interrogated for up-to-date commercial information at any time. A feature-rich database which can be configured and customised to suit your business. Straight-forward and easy to use, it’s been designed with pharmaceutical sales organisations in mind with add-ons and development propositions tailored to your company’s needs. Always accessible, actisCRM allows rapid interaction through desktop and mobile applications that suit every part of your business, from traditional face-to-face call reporting, through key account management and medical sales liaison to management at all levels.

DXC FirstDoc™: Support research and development (R&D), Quality and Manufacturing (Q&M) and Quality Management System (QMS) with simple navigation, task management and collaboration.

Enquire is a powerful and customizable query search tool designed for pharmaceutical sales reps and office personnel that can quickly and efficiently answer specific questions and challenges. It has pre-bucketed query fields that are customized based on a company's unique needs. Enquire can help office support teams build and export any sort of report, making it a valuable tool for improving efficiency and solving problems. PDS can create a custom Enquire dashboard for a business within 6-8 weeks, providing a seamless way to access information and improve operations and sales support.

ClinicalWave.ai built on AWS cloud platform is an integrated AI platform tailored for life sciences organizations. It offers automated redaction and extraction of sensitive data and leverages cutting-edge NLP technology to extract valuable insights from clinical documents, streamlining your workflows like never before. It consists of: 1. ClinRedact AI- Our Redaction product which automatically identifies and redacts sensitive information in clinical documents, saving time and ensuring data integrity. 2. ClinExtract AI- The AI Data Extraction product that utilizes NLP and machine learning to extract relevant data points from clinical documents, providing valuable insights and streamlining workflows. 3. ClinDICOM AI- Experience the power of our feature-rich DICOM data extraction and redaction product offering targeted redaction, customizable rules, intelligent contextual analysis, audit trail compliance, redaction preview, and a user-friendly interface.

ActivityBase is the established industry software platform for screening data management, with feature-rich data analysis tools, built-in object/compound registration tools and the industry standard database. ActivityBase provides analysis support for a wide range of biochemical, cellular and biophysical assay formats (including Ion Channel, FLIPR, Kinetic, SPR, Mass Spectrometry assays). The system integrates into HCS imaging stores (Perkin Elmer Columbus, Thermo Fisher HCS Studio, Molecular Devices MDCStore) for easy import of data and images. ActivityBase also features built-in compound registration and plate management tools. With ActivityBase, you can easily track and manage the results from years of assays in one system. The system can be configured to meet your needs, without having to buy new analysis packs, and, through improvements in your data analysis processes, can even increase your lab analysis tenfold.

Experiment with conventional behavioral apparatuses or customize your own. Identify behaviors selective to each pre-determined or unknown testing groups. Through the dynamic chart, various elements according to the actions are visualized.

ConcertAI is a leading provider of AI-powered solutions in the healthcare industry, specializing in oncology. Their mission is to accelerate insights and improve outcomes for patients through leading real-world data, AI technologies, and scientific expertise. ConcertAI offers a suite of products and services designed to enhance clinical research and patient care. Their Real-World Data Products provide comprehensive, fit-for-purpose datasets that support a variety of research needs across the enterprise. The digital trial solution streamlines clinical trial processes, while the Clinical Trial Optimization (CTO) platform utilizes large-scale AI to refine trial design and execution in oncology and hematology. In collaboration with NeoGenomics, ConcertAI has developed CTO-H, a SaaS solution focused on hematological malignancies, offering advanced research analytics and operational optimization.

Clinithink is a leading healthcare technology company specializing in artificial intelligence solutions that transform unstructured medical data into actionable insights. Our patented CLiX platform utilizes Clinical Natural Language Processing (CNLP) to interpret complex clinical narratives, enabling healthcare organizations to enhance patient care and operational efficiency. Clinithink offers tailored solutions across life sciences, revenue cycle management, and population health, addressing challenges such as patient cohort identification, reimbursement optimization, and disease progression tracking. Clinithink's innovative technology has garnered trust from leading pharmaceutical and healthcare organizations worldwide, positioning it at the forefront of healthcare AI and digital health advancements. CLiX is capable of understanding a vast quantity of unique and detailed clinical concepts such as; certainty, severity, laterality, and temporality.

Over the last several years, the Life Sciences industry has faced nearly $15 billion in fines and compliance-related settlements, making it critical for companies to adhere to pharmaceutical, medical device and biotech best practices. Efficient and effective management of clinical trials can also significantly impact the time, scope and budget for the development of a drug or medical device. With OpenText™ Clinical Trial Quality Management System (ctQMS), companies can remain compliant, reduce costs of records management and establish best practice through collaboration before, during and after the clinical trial lifecycle.

Deliver explainable imaging AI faster and more accurately with Zegami. Our full-stack service enables researchers, data scientists and medical practitioners to deliver explainable imaging AI with greater efficiency and accuracy. Our team and tools become your data science plug-in, to ​create, enhance and validate machine learning models in healthcare, life sciences and manufacturing, to drive your business or project forward.​

Single-Source-of-Truth commercial data management service with fully integrated customer master data management and business intelligence. Pharma companies don’t have to choose between the high price and long timelines of a consulting engagement or the heavy overhead and operational limitations of SaaS solutions. Mosaic clients get the high touch service and customization of a consulting engagement with the more predictable cost of a SaaS solution.

Novatek International offers comprehensive software solutions that meets and exceeds the quality and compliance requirements for the life science industry. The process-specific offerings are an integrated platform that provides consistency and standardization across multiple departments within a site, and across multiple sites. This greatly reduces the total cost of ownership and results in a higher ROI. NOVA-CPM is a state-of-the-art automation tool that provides full management of your equipment qualification, calibration, and maintenance processes. The system is designed to ensure global regulatory compliance and data integrity, with security and electronic signature and audit trails. NOVA-CPM is the leading Computerized Maintenance Management System (CMMS) solution that provides functionality for the full life cycle of equipment, from purchase and validation, calibration and maintenance operations, repairs, and end-of-life replacement.

Scitara DLX™ offers a rapid connectivity infrastructure for any instrument in the life science laboratory in a fully compliant and auditable cloud-based platform. Scitara DLX™ is a universal digital data infrastructure that connects any instrument, resource, app and software in the laboratory. The cloud-based, fully auditable platform connects all data sources across the lab, allowing the free flow of data across multiple end points. This allows scientists to devote their time to scientific research, not waste it solving data issues. DLX curates and corrects data in flight to support the development of accurate, properly structured data models that feed AI and ML systems. This supports a successful digital transformation strategy in the pharma and biopharma industries. Unlocking insights from scientific data enables faster decision-making in drug discovery and development, helping bring drugs to market more quickly.

Axtria DataMAx™ is the next-generation global cloud-based commercial Life Sciences data management product enabling accelerated actionable business insights from trusted data. Axtria DataMAx™ facilitates the rapid integration of all major structured and unstructured life sciences data sources, securely, accurately, and with industry compliance. Data quality and business management rules are applied to make sure the data being processed is conditioned for its intended use and can be trusted. Users can provision data mart creation for downstream consumption and reporting by analytics systems, models, or individual data stewards.

Scilligence’s RegMol is an entity registration and bioassay database which supports all entities. Our comprehensive and easy-to-deploy platform enables centralized management of protocols and assay data to support all research and development collaborations. RegMol empowers data driven decisions through our powerful data mining analytics including query by chemical structure, HELM and biosequences. Our innovation is driven by the idea that the best solutions come from shared experiences. We’ve built a tool that makes it easy to share knowledge and resources with colleagues globally. We understand that it can be difficult to wrangle all of the data you need to make industry-changing discoveries. Our ELN is a flexible web platform that allows you to easily find and organize unstructured data. Our advanced search and indexing capabilities allow researchers to quickly search and filter through unstructured data.

Trusted by the global life sciences industry to drive intelligent engagement. Improve customer experience with intelligent HCP engagement in real-time across all channels. Leverage data science and embedded intelligence to deliver the most effective, timely messages to customers. Ensure field teams have the most up-to-date information and insights to plan and execute calls. Build deeper customer relationships with compliant note capture. Tailored insights at the point of execution via pre-built and custom visualizations. Veeva CRM provides flexibility for commercial organizations to implement artificial intelligence how they want. Veeva CRM Suggestions provides an open model to implement next best actions using any data science provider.

A web based software that uses Quality Risk Management to organize, analyze and trace Quality information directly to the specific risk it represents to the patient and drug product. Why Us? CINCO, a risk-based quality management software for the Life Sciences Industry. It provides paperless traceability of every critical to quality aspect of a drug or medical device to enable transparent quality decisions at every moment. Why Risk Management? Quality Risk Management is methodology that provides an objective approach into identifying and mitigating the risks of a drug or medical device manufacturing process. It is currently required by most regulatory agencies. However, the paper-based approach the Life Sciences Industry currently uses its ineffective in managing the significant and valuable risk data. It is prone to errors, introduces too much friction to the users and ends up not adding the potential value to the operations. On-demand access to what is critical to the product qua

Faster more precise accounting, accruals, and FP&A Software that harnesses real-time clinical trial data and third-party vendor collaboration. Thoughtfully designed by biotech finance and audit experts who have been in your shoes: 1) Automate and expedite clinical accruals - Stop wrangling data and manually updating trackers and spreadsheets. We integrate real data to drive clinical accruals, saving you significant time and money. 2) Hold vendors accountable - Trusting vendors with timely, complete and accurate updates can be challenging. Condor “audits” your vendors, with documentation and evidence. 3) Improve your audits - Auditors at the Big Four love Condor. We bring peace of mind to critical audit matters. 4) Empowering cross-functional alignment - Build trust and shared understanding between clinical, finance, and third parties with a single source of truth. 5) Powerful financial insights and scenario cash planning - Help leadership make data-driven decisions.

anicomply is an eBR-first Intelligence Platform for regulated manufacturing. It uses existing, structured Microsoft Word recipes and manufacturing instructions as the starting point for executable digital batch workflows, rather than simply displaying paper forms on a screen. Declarative, no-code-oriented design helps process teams create and adapt workflows with less dependence on programming. Depending on configuration, audit trails, electronic signatures, version control and four-eyes review support controlled execution and traceability. Structured data can support QA review by exception. The browser-based platform supports cloud or on-premises deployment and German and English user interfaces. Integration with existing ERP, MES, and SCADA environments is scoped to the specific project. Available functionality depends on the agreed scope and configuration. Explore your own Master Batch Record in a structured demo or Proof of Value.

Qualitum is an agentic platform for computer system validation (CSV/CQV) in regulated life-sciences. It drafts IQ/OQ/PQ protocols, GAMP 5 classifications and audit trails straight from source documents (URS, P&IDs, SOP libraries), with every requirement traced end-to-end through a queryable graph that replaces spreadsheet RTMs. All ALCOA+ data-integrity criteria are monitored on every record, not samples, with humans reviewing and approving agent output. Qualitum runs single-tenant on AWS, Azure or on-prem, with customer-managed keys and no training rights on customer data, and connects to systems of record already in use (Veeva, MasterControl, TrackWise, AVEVA PI, Tulip and others). Built for Heads of Validation and validation consultancies at pharma, biotech and medical-device companies. Annual per-site licence, quoted on request; an 8-12 week fixed-fee pilot (one system) is available.