Alternatives to Tricentis Vera

Software testing must be centrally managed and visible from conception to production in order to make software releases more secure and faster. Tricentis qTest enables teams to collaborate and ship faster, with less risk, by unifying, managing, and scaling testing across the enterprise. Robust testing includes a variety of testing tools, teams, test types, and testing methods. Tricentis qTest combines them all so that teams can release more confidently and reduce risk. It also helps identify opportunities to move faster - collectively. Automate more testing, increase the release velocity, and bring together teams throughout the software development process. Native DevOps integrations such as Jira, Jenkins and GitHub keep QA and development in sync. With a full audit trail, trace defects and tests back to development and requirements. Align teams with cross-project reporting.

QBench allows you to keep track of all your samples and where they are located in the workflow using a single system. QBench eliminates the need for spreadsheets, shared folders in the network, and paper-based tracking systems. You can view hundreds of PDF reports/COAs before publishing or emailing. You can generate barcodes and create labels that you can customize for your samples. Compatible with standard printers and scanners. QBench's billing module allows you to create and send invoices right from the system. You can see counts and latencies for different data types in QBench. This includes metrics like turnaround time, sample counts per test, sample delay, and many others. QBench makes it easy for you to gather the data your lab needs for the assays you perform.

Labguru, a cloud-based Electronic Lab Notebook, LIMS and Informatics Platform that offers a complete solution to life science research and industry, is secure and reliable. It records and manages laboratory data, inventory, molecular biology tools, and chemistry tools. This allows labs to run more efficiently and automates lab operations. Labguru allows scientists to design experiments and workflows. They can also capture structured and unstructured information, manage projects, and share their results. You can create custom-designed experiment templates and integrate protocols, SOPs and other cutting-edge features to improve data quality, streamline workflows, and reduce costs. Labguru is available via the cloud on desktops as well as mobile devices. Labguru is part Holtzbrinck Publishing Group. It serves more than 100,000 scientists from universities, research institutes, startups, and large pharma companies around the world.

Unify quality processes with QT9's all-in-one cloud-based QMS Software Suite. QT9 QMS is a user-friendly quality management software that includes 25+ modules with unlimited scalability. Automate ISO & FDA Compliance with email alerts, To Do lists and FDA 21 CFR Part 11 Compliant Electronic Approvals. QT9 QMS enables Life Sciences, Biotechnology Companies, Medical Device Manufacturers and Pharmaceutical Companies to digitally transform operations. Get real-time status updates and visualize quality metrics up-to-the-minute. QT9 QMS comes with built-in document control, revision-level controls, corrective actions (CAPAs), Nonconforming products and more. Advance product releases with Deviation Management, Engineering Change Orders, FMEA, Inspection Management Modules Included. Go paperless & put time-consuming tasks on autopilot. QT9 QMS comes ready-to-use. Get a free product tour! Start a Free Trial. Visit QT9qms.com

Vault Training helps ensure job readiness and compliance through the creation and management of role-based training requirements. Vault Training unites document management and training. It allows life sciences companies to manage authoring approval, assignment, assignment and assessment of critical training materials from one place. You can easily manage your training content and deliver time-sensitive assignments using a single suite of quality applications. You can easily assign tasks based on your job function or role. You can track and complete training tasks, or monitor status via a role-based homepage. Training tasks can be triggered by quality events such as approval of content changes, CAPA plans or periodic reviews. Automate training assignments based upon job functions and roles. You can track, monitor, and demonstrate the competencies of your employees. You can also see the status of your training assignments with delivered dashboards or reports.

Logilab® ELN from Agaram is a proven Electronic Lab Notebook (ELN) solution that offers laboratories the ability to become completely paperless by recording, executing, and storing their tests, experiments, and lab tasks in a secure database. This ELN solution is suitable for laboratories operating in various scientific fields, as well as researchers and organizations engaged in regulated and non-regulated product and project development. Logilab® ELN helps laboratory organizations achieve higher productivity, better quality, and compliance with various statutory standards and Good Lab Practices (GxP) principles of data integrity. The product includes several features to assist laboratories, such as a simple interface to design lab templates for tasks and experiments, dynamic inventory management with re-order levels and expiry dates, barcode printing, and inventory validation, user-configured dynamic reports, and document creation. It also automates instrument data capture, enabling the parsing of data from instrument output files and port-based instruments, making it a valuable asset to any laboratory.

The AssurX platform is a powerful software platform for enterprise quality management (EQMS) and regulatory compliance to reliably communicate and coordinate information, documentation, and activities. AssurX allows regulated businesses to quickly identify and control quality issues and risk exposure to avoid quality or noncompliance problems while improving workflow. AssurX QMS software is uniquely configurable to fit any established or dynamic business requirements. The system creates an electronic workflow of tasks, alerts, escalations, and approvals that can be automated to the desired level, mapping precisely to real-world operations. No other system is easier to deploy, configure, and modify. AssurX solutions integrate seamlessly to create a connected quality system. Solutions include audit management, corrective actions, training management, compliant management, document management, change control, risk management, EHS incident management, and more.

Novatek International provides software solutions that meet or exceed the compliance and quality requirements of the life science industry. The process specific offerings provide an integrated platform that allows for consistency and standardization across multiple departments within a single site and across multiple sites.

Meet the cutting-edge validation solution which automates, unifies and accelerates success. Res_Q helps IT leaders and quality managers eliminate validation debt, gain peace of mind, untangle valuable resource, and achieve financial freedom. Res_Q’s data-focused architectural approach and wide range of industry-supported apps prevent you from getting deeper into validation debt each time a new software release is released. The open API approach enables a bidirectional data flow, which is useful for system integrations, migrations during onboarding and more. Workflows that can be configured to match your operational needs and integrate industry best practice. All validation processes can be controlled by a single system that serves all areas of the enterprise including IT, manufacturing and lab systems. Workflows can be initiated and workloads assigned based on the risk profile. Res_Q prioritizes quality without sacrificing speed.

Kalypso offers life sciences companies a cost-effective accelerator to implement a RIM system - Accel for RIM. The integrated platform allows for efficient product distribution and management, as well as a global platform to track and manage product registrations. It consolidates compliance data and quality data from different enterprise solutions into one global source of truth to facilitate product registrations and tracking in order to speed up regulatory submissions. Modern APIs are used to combine product data, regulatory documentation, and submission packages. Pre-configured for quick implementation with a valid software system. Based on industry-leading RIM practices.

Revolutionize your Life Sciences processes. You can dramatically improve the quality, control, and efficiency of your products and processes. Our fully compliant platform is pre-validated according GAMP5. This ensures inspection readiness at all time. You have complete control over all documents and processes. You can also customize workflows and automate when possible. You can enjoy uninterrupted workflows and full traceability with seamlessly connected and integrated modules. Our dedicated team is available to answer any questions you may have. Only the best Scilife experience is possible! Our Scilife platform automates, automates and organizes all processes in your industry space, no matter if you're in Medical Devices or Pharma & Biotech or ATMP. Click below to see which Scilife modules are available for your industry's unique lifecycle stages.

End-to-end regulatory information management from a single platform. The Vault RIM Suite streamlines global regulatory process on a single cloud-based platform. This allows life sciences companies to increase visibility, data quality, agility, and efficiency. You can respond faster to changes in regulations and improve process efficiency, from submission planning to publication. Coordinate regulatory efforts across HQ and affiliates within a single RIM platform. Assure that teams are creating reliable regulatory content with high data integrity. Veeva Vault Registrations manages product data worldwide, including variations, registration status, and interactions with health authorities. Veeva's flexible data structure supports IDMP data points, and will continue to support changing regulatory data standards. Veeva Vault Submissions automates regulatory process steps and streamlines submission planning.

A robust platform for automatic variant prioritization and clinical interpretation, as well as report generation, is essential to ensure efficient reporting of NGS-based clinical trials. Strand Omics, a cloud-based platform that is HIPAA-compliant and fast, drives our clinical diagnostics practice. It has been refined over 4 years with over 10,000 clinical reports and multiple peer reviewed publications. Strand Omics is a combination of bioinformatics algorithms and curated databases, visualization interfaces, and reporting capabilities. It offers specialized workflows that can be used for rare inherited disorders and somatic tumor profiling tests. The platform has over 10,000 variants curated to oncogenicity, 100 genes that are curated for druggability across multiple types of cancer, and 500 drugs that have been curated for evidence.

The Life Sciences industry has been subject to nearly $15 billion in compliance-related settlements and fines over the past few years. It is therefore critical that companies adhere to best practices in pharmaceutical, biotech, and medical device manufacturing. A well-managed clinical trial can have a significant impact on the development time, budget, and scope of a drug or medical device. OpenText™, Clinical Trial Quality Management System, (ctQMS) allows companies to remain compliant, reduce the cost of records management, and establish best practices through collaboration during, and after, the clinical trial.

Concentriq, our AI-powered platform for software, sits at the intersection between digital and computational pathology. It connects functionality required to perform routine pathology operations with powerful AI applications to accelerate breakthroughs to improve patient outcomes. Laboratories around the world recognize the challenges we face today: a rising cancer burden and a shortage in pathologists. They also need to modernize quickly due to declining reimbursements and declining reimbursements. The time is right to grab this moment, as one billion pathology slides will be digitalized each year, creating vast amounts new data and information. Digital pathology gives today's forward-thinking pathology organisations the tools to overcome their collective challenges and fundamentally change how they work and contribute to medicine.

OpenText™, a leading provider of information management solutions for life sciences organizations, helps them to harness insights from data and content to improve their decision-making and accelerate product development. Integrate, manage and securely exchange data between people, systems, and things. Use information assets to drive innovation and commercialization. Cloud-native software can run anywhere, giving you freedom of choice. OpenText for life sciences accelerates discovery by delivering actionable insights that can be used to drive innovation in pipelines. Intelligent capture allows you to capture and manage research papers in electronic lab notebooks. Text mining can help you gain insights. Unstructured text in clinical trial reports, study protocol, clinical safety and efficiency findings, can be used to extract knowledge. Learn how to intelligently analyze and classify clinical trial documents and extract them to reduce the risk for costly stops and starts.

MonQual QMS includes pre-built, DMS, and LMS systems. It can also be integrated with other stand-alone systems. Integrate your LIMS (Laboratory Information Management System), MES(Manufacturing Execution System), SAP (Warehouse Management System), and other systems. This is true for both legacy and new applications. MonQual is everything your team wants. It combines quality, compliance management, business intelligence tools, and business productivity. You can take care of your documents and comply with regulatory standards by using the integrated DMS and LMS services. Quality deviations are part of the process, but we can prevent them from happening in the future. MonQual has processes that can detect deviations early, track them, run a root cause analysis, and then record and document them to prevent future ones.

GHSAuth by Mar-Kov Computer Systems, a robust Global Harmonized Standard compliant Safety Data Sheets (SDSs) and Safety Label authoring software for chemical manufacturers, is available. GHSAuth allows EH&S staff to manage and organize SDS files for their organization, access a list of hazard codes, precautionary phrases, track changes and achieve revision control. You can choose from both a free and a paid version of the software package.

THINQ is a thought-leader in compliance for the Life Sciences sector. They provide compliance solutions to a wide range of pharmaceutical, biotechnology, and medical device companies. THINQ has a special expertise regarding validation and is leading the change in how validation is managed within Life Sciences companies. THINQ provides comprehensive compliance program management and development--powerful, market-proven solutions that are custom-tailored to our enterprise clients.

Combining the multiomic data and medical history of an individual to deliver more personalized healthcare. Use purpose-built databases to support large-scale analyses and collaborative research across populations. Accelerate your research with scalable workflows, integrated computation tools and integrated computing. Protect patient privacy by ensuring HIPAA compliance and using built-in data access, logging and logging. AWS HealthOmics enables healthcare and life sciences organizations and their software partner to store, query and analyze genomic, transcriptionomic, or other omics data, and then generate insights using that data. Store and analyze omics for hundreds of thousands patients to understand the relationship between omics variation and phenotypes in a population. Create reproducible and traceable workflows for clinical multiomics to reduce turnaround time and increase productivity. Integrate multiomic analyses into clinical trials to test out new drug candidates.

The regulatory affairs departments in the healthcare and life science industry are driven to improve efficiency and create intelligent systems that optimize costs, maximize accuracy, and reduce submission times. RIMTrack, a cloud-ready, artificial intelligence (AI)-based, new age regulatory information management system, addresses this concern. It was created from scratch to assist organizations in preparing submissions accurately and efficiently. It streamlines regulatory processes related to licensing, approvals, regulatory, competitive intelligence, clinical trials and reporting across global stakeholders. Integrate with existing RIM systems to achieve complete management of the regulatory lifecycle process.

Zegami makes it easier to deliver explainable imaging AI more quickly and accurately. Zegami's full-stack service allows researchers, data scientists, and medical professionals to deliver explainable AI with greater efficiency. Our team and tools are your data science plug-in to create, validate, and enhance machine learning models in healthcare, life science, and manufacturing to propel your business or project forward.

All researchers from different industries can use the same environment! ResearchManager is a platform that allows researchers to access all functions and information from one place. They can also share it with others. This platform is for researchers who are ready for the future. Future where patient and data access and sharing are central. We provide support for everyone involved in research in the life sciences sector. This is done through an online platform that includes the eClinical tools EDC and CTMS & ERMS. This allows researchers to share data and facilitates research at a higher level. We are also experts in the fields of data validation, enrichment, and collection.

Easy lab management. Streamline communication, consolidate orders, and track inventory. Quartzy is the leading platform for R&D lab productivity. We help you manage the unique workflows of a lab - order, order, inventory, and optimize your resources to ensure your next experiment doesn't get delayed. Quartzy is more than a cloud-native software solution. It's a fully-integrated distributor of lab products, giving scientists and lab managers the ability order more than 10,000,000 products (including consumables and chemicals, office supplies, and more) from over 1,800 top brands. It's as simple as 1-2-3 to simplify your ordering process. In just two clicks, lab members can browse our 10 million-strong catalog or create custom orders for their lab manager. You can manage incoming supply requests and approve them or make an immediate purchase.

Mednet is an eClinical technology company that specializes in healthcare solutions for the global life science community. Mednet's flexible, EDC-centric eClinical platform increases the efficiency of clinical research of all sizes. Mednet's comprehensive solution suite provides all the tools necessary to create and manage clinical research. It can also adapt to changing demands and requirements. Mednet has been trusted by CROs in every sector of the pharmaceutical, medical device, and biotechnology industries for almost 20 years. They provide the expertise, reliability, and innovation that they need to succeed. Mednetsolutions.com has more information.

Unstructured health data can be unified and liberated with Interactive AI and NLP solutions that deliver health insights to Providers. Payers. Life Sciences. Interactive AI and NLP solution to unlock healthcare insights from unstructured clinical data. Provider. Accelerate data abstraction and clinical validation of clinical notes information. Reduce time and costs needed to identify care gaps, review care quality dashboards and create registry reports. Payer. To better manage high-risk and high-cost member cohorts, integrate and analyze claims data and clinical notes. Life Sciences. Use clinical trial databases and data taken from clinical notes to quickly match patients with clinical trials. Real world clinical data and evidence can be leveraged. Ember is a complete solution that combines NLP and predictive analytics. Streamline. Healthcare Analytics for Unstructured Data to Improve Quality and Efficiency.

In today's pharmaceutical manufacturing environment, it can be difficult to maintain consistent product quality and quality processes. To meet regulatory requirements, industries like the Pharmaceutical, Biotech and Life Sciences must maintain Good Manufacturing Practices (GMP). You must not only meet GMP requirements, but you must also be capable of proving it.

Create your own behavioral apparatuses, or experiment with those that are already available. Identify behaviors specific to each predetermined or unknown test groups. The dynamic chart allows you to visualize various elements based on the actions.

A platform that connects scientific reasoning, compound design, computational resources, and other relevant information. The Design Hub by Chemaxon for medicinal chemistry, from analysis to prioritization. One platform to design compounds and manage ideas. One platform that links scientific rationale, compound design, computational resources, and other information. You can switch from PowerPoint files to graphical or chemically searchable hypotheses, which are integral parts of compound design. You can easily work in a rich visual environment with your trusted physchem properties, computational models or novelty issues. This secure online service allows you to involve your CROs in compound progression. Analyze the evidence from biological assays and experimental structural information to extract SAR and create new hypotheses for each optimization iteration. Your scientific hypotheses can be stored in a "designer’s ELN" (chemically-aware drawing canvases).

NVIDIA®, Parabricks®, is the only GPU accelerated suite of genomic analysis apps that delivers fast, accurate analysis of exomes and genomes for sequencing centres, clinical teams and high-throughput instrument developers. NVIDIA Parabricks provides GPU-accelerated versions of tools used every day by computational biologists and bioinformaticians--enabling significantly faster runtimes, workflow scalability, and lower compute costs. NVIDIA Parabricks can accelerate runtimes in a variety of hardware configurations, from FastQ to Variant Call format (VCF). This is done with NVIDIA Tensor Core GPUs. Genomic researchers will experience acceleration at every step of their analysis workflows - from alignment to sorting and variant calling. The compute time can be accelerated up to 107X when more GPUs are added.

The Suite is secure and scalable. It features an intuitive interface that allows scientists to configure workflows for any technique, modality, or data type. Signals VitroVivo 3.0, formerly Signal's Screening, transforms raw data into actionable findings. Signals Inventa 3.0, formerly Signals Lead Discovery is the next-generation analytics software that allows researchers to seamlessly publish results across disparate data sources. A cloud-based electronic notebook that is easy to use allows for experimental data capture, materials management, collaboration workflows, and more. Flexible visual and automated instrument data processing to improve data quality and reproducibility. Rich interactive analytics and unified data management for scientific research results. Integration with partner systems and processes as well as internal systems is possible.

Our cutting-edge platform, the Medidata Clinical Cloud, transforms clinical trial experiences for patients, sponsors and CROs. The Medidata Clinical Cloud is the only unified technology platform that focuses exclusively on clinical research. It addresses every step of the research process, from start to finish. Our platform helps medical device and life science organizations reduce development costs, minimize risks, and bring treatments and devices to market quicker. The Medidata Clinical Cloud will allow you to access the power of any product you choose for your clinical trials program. Medidata is leading the digital transformation in clinical research. Our platform, powered by artificial intelligence, machine-learning, advanced analytics, and advanced research, brings together researchers, study managers and investigators to accelerate research. Obtain regulatory-compliant, patient-friendly electronic informed consent for clinical trials.

Pharmagin's technology offers life sciences companies and medcomm agents Smarter Pharma Marketing. Our web-based platform solution is customizable and can be customized to manage compliance and logistics for key opinion leader (KOL), education programs. It uses a data-centric approach that delivers improved program ROI, deeper HCP relationships, and better patient outcomes. Our SaaS technology expertise spans over a decade. Clients rely on our ability to be responsive, innovative, and agile.

PatientIQ was founded in Chicago, Illinois. It serves providers, payers, and medical device & health sciences companies. The largest platform for healthcare professionals to connect and improve patient outcomes. Provide healthcare professionals with the industry's best technology to practice data-driven medicine. All stakeholders in the U.S. healthcare system are under increasing pressure. Objective measures of patient outcomes are crucial to assessing "value". Although measuring outcomes can be complex, time-consuming, expensive, and complicated due to technological barriers, they are the most valuable currency for value-based healthcare in the future. The next big market opportunity for digital health is a transparent way to measure, analyze, compare, and compare outcomes across stakeholders.

Signals Inventa is a next-generation data management platform for scientific results analysis. It is powered by PerkinElmer’s Signals Data Factory technology, which allows you to quickly access and analyze all scientific data collected during the research and development process. Signals Inventa can help you determine which tests are most effective, what next to perform, what you should test, and much more. Signals Inventa makes data ready for exploration by staging, normalizing, and staging it. Signals Inventa expands scientific understanding with a range of scientific-analytical methods, including R-group decomposition, chemical clustering, matched molecular pair analysis, maximum chemical substructure, blast search of both internal and external databases, and sequence alignment.

TraceLink is the most prominent digital platform company in the life science supply chain. It brings together hundreds of thousands of healthcare and pharmaceutical organizations for the greater good for patients. TraceLink's digital solutions provide the visibility, precision, and agility necessary to enable all members of the pharmaceutical industry to thrive in a world that is constantly changing.

JADBio is an automated machine learning platform that uses JADBio's state-of-the art technology without any programming. It solves many open problems in machine-learning with its innovative algorithms. It is easy to use and can perform sophisticated and accurate machine learning analyses, even if you don't know any math, statistics or coding. It was specifically designed for life science data, particularly molecular data. It can handle the unique molecular data issues such as low sample sizes and high numbers of measured quantities, which could reach into the millions. It is essential for life scientists to identify the biomarkers and features that are predictive and important. They also need to know their roles and how they can help them understand the molecular mechanisms. Knowledge discovery is often more important that a predictive model. JADBio focuses on feature selection, and its interpretation.

Amazon Comprehend is a HIPAA-eligible, natural language processing (NLP), service that uses machine-learning to extract health data form medical text. No machine learning experience is necessary. Today, a lot of health data is found in free-form medical texts like doctor's notes, clinical trials reports, and patient records. Manually extracting data can be time-consuming and automated rule-based attempts at extracting data won't capture the whole story because they don't take context into consideration. The data is not usable for large-scale analytics that will help improve the healthcare and life sciences industry, patient outcomes, and increase efficiencies.

Your sales reps should be able to see more doctors through Ammras organizer. A sales representative's effectiveness is measured by their ability to show the right materials at the right time. Ammras can help your representative do just that. It provides life science companies with the decision-support tool that analyzes real time market data, channel activity, and HCP (Healthcare professionals). This tool is designed to provide life sciences companies with insight, clarity, guidance, and the ability to deliver the right information at exactly the right moment. It uses data to extract only the most relevant and valuable information at the time of decision-making and present it to you and your field team. Our team focuses on simplicity and usability, so they can sell by making the most of their time to establish a strong relationship.

IDBS Polar is the first BioPharma lifecycle management (BPLM) platform in the world. It eliminates repetitive manual tasks and allows you to execute your processes efficiently while curating data. This will allow you to accelerate the time to market, by tackling the most challenging challenges of process design, optimization scale-up and technology transfer. Interactive data analytics applications such as bioreactor comparision designed specifically for biopharmaceutical development scientists. IDBS Polar is an integrated platform that manages drug progress in contexts such as workflow, integration and insight. Workflows designed for the BioPharma lifecycle, with process-aware design, planning, and execution. Integrations that give meaning to your data. Rapid integration into your development environment, enabling automation, and curating a data backbone based on processes.

ysura conceives and develops innovative Sales and Marketing Solutions for the Pharmaceutical Industry and offers them as a Software-as-a-Service. Founded in 2012, ysura is based in Munich. It employs over 60 people from 17 countries. Ysura, an old Celtic word meaning Isar, is the name of the river that flows through Munich. It is a combination of ys (fast water) and ura(water). Ysura is short for fast water. Our products are fast and adaptable to the flow of information and tasks in the life sciences industry.

The biopharmaceutical market is complex today. There are growing demands for better specificity and safety, new treatment classes, and more complex mechanisms of disease. To keep up with this complexity, we need to have a better understanding of therapeutic behavior. Simulation and modeling provide unique opportunities to explore biological and physical processes down to the atomic levels. This can be used to guide physical experimentation and accelerate the discovery and development process. BIOVIA Discovery Studio brings together more than 30 years of peer reviewed research and world-class in-silico techniques like molecular mechanics and free energy calculations. It also allows for biotherapeutics developmentability and other related topics into one environment. It gives researchers a complete toolkit to explore the nuances in protein chemistry and to catalyze the discovery of small and big molecule therapeutics, from Target ID to Lead Optimizement.

Model N is an end-to-end platform that empowers companies to maximize their revenue by transforming Sales, Marketing, Channels and Finance. Model N's revenue management solutions can help you maximize your revenue by turning tactical, siloed activities into strategic, end-to-end revenue processes using automation and intelligence. Revenue Cloud bridges the gap between back-office and front-office activities, providing a single system of record for all revenue execution. Customers can easily set up and quote complex products, quickly reach terms on complex contracts, have better channel data, which allows for visibility into channels and efficient management of incentive programs, avoiding overpayments. Model N Rebate Management allows you to better engage your channels and maximize revenue.

Cytobank, a cloud-based platform that allows for analysis, storage, sharing, and sharing of mass cytometry data, is available. Cytobank can be accessed via the internet using a web browser and an existing account. Cytobank does not require any additional software or hardware to be installed, updated, or maintained. Both license types have the same functionality. This license is ideal for large research groups, pharma, biotech R&D teams, clinical research organizations, and other clinical research organizations. Private Cloud, Access is controlled by an administrator role. Larger compute caps for functionality such as viSNE

SANeForce offers a comprehensive CRM and sales force automation solution, primarily tailored for the pharmaceutical, healthcare and life sciences industries. SANeForce is designed to increase the productivity of marketing and sales teams. It offers features such as real-time order tracking, expense tracking, stock control, and territory administration. The platform supports medical representative reporting, allowing field sales personnel log visits, capture doctor interaction, and manage appointment directly from their mobile device. SANeForce's data-driven insights, analytics, and customer engagement strategies help organizations track performance, streamline their processes, and optimize their customer engagement strategies. The solution also includes features for compliance, making it an ideal choice for highly-regulated sectors that require meticulous records and adherence to standards.

PharmaWorx allows you to close the loop between customer feedback and marketing activities by providing real-time data capture. This also increases customer relationship. PharmaWorx allows Med Reps to make an informal or planned visit to a doctor's offices, and then instantly switch on their iPad/Android tablet to present product information to the doctor. They can also complete previously recorded tasks, take notes, or complete previous tasks. A doctor may be interested in a specific image, video, or brochure. The med rep can instantly switch on their iPad or Android tablet while they are still at the doctor's offices and present product information to them. They can also complete previously recorded tasks or capture notes for the current visit.

ClinicalWave.ai, built on AWS' cloud platform, is an integrated AI platform designed for life sciences companies. It uses cutting-edge NLP to extract valuable insights and automates the redaction and extraction sensitive data from clinical documents. It is made up of: 1. ClinRedact AI - Our Redaction Product that automatically identifies and removes sensitive information from clinical documents. This product saves time and ensures data integrity. 2. ClinExtract AI - The AI Data Extraction Product that uses NLP and Machine Learning to extract relevant data from clinical documents. This product provides valuable insights and streamlines workflows. 3. ClinDICOM AI - Experience the power and features of our DICOM data extraction product. It offers targeted redaction, customizable redaction rules, intelligent context analysis, audit trail compliance and a user friendly interface.

StarDrop™, a comprehensive suite of integrated software, delivers the best in silico technology within a highly visual interface. StarDrop™, which allows seamless flow between the latest data, predictive modeling, and decision-making regarding the next round or synthesis, improves the speed, efficiency and productivity of the discovery process. A balance of different properties is essential for successful compounds. StarDrop™, which guides you through the multi-parameter optimization challenge, helps you target compounds with the highest chance of success. It also saves you time and resources by allowing you to synthesize fewer compounds and test them less often.

Within3 is the leader in insight management for life science teams. Our insights management platform helps identify the right people, engage them and deliver answers that enable informed, agile decision-making. Our platform was created to address the life science insight gap. Companies often base decisions on outdated or incomplete data, which can lead to huge losses in time and money. Within3's insight management platform closes the gap in product development. It can be used at all stages of the product development process, including planning, recruiting, understanding, and analysis. Within3 is trusted by the world's leading pharmaceutical companies and medical device companies to identify key professionals, engage audiences in focused discussions, gain a 360-degree view on scientific and market signals.

Axtria SalesIQTM is the most popular sales planning and operations software for the global life science industry. It enables motivated sales teams to achieve greater commercial success. Axtria SalesIQTM empowers sales reps to make smart decisions and reach the right customers at a time that suits their needs. Simulating and what-if analysis allows you to seamlessly convert brand strategy into sales plans. You can launch any drug or medical device in any therapeutic area quickly and with total flexibility. Transform from product-centric to customer centric omnichannel interactions. Connect the dots between providers and territories, channels, incentives, and incentives. You can improve decision-making by leveraging trusted data from ingestion to insights.