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Mednet is a healthcare technology company specializing in eClinical solutions designed for the global life sciences community. Pharmaceutical, medical device, biotechnology and Contract Research Organizations (CROs) around the world have trusted Mednet for over 23 years to deliver the technology innovation, experience and reliability they need for success. Mednet’s comprehensive, EDC-centric eClinical platform, iMednet, optimizes clinical studies of all types and sizes – accelerating research with exceptional flexibility, ease-of-use, robust functionality, affordability, and stellar support. iMednet is feature-rich and uniquely designed to help sponsors and CROs get studies up and running quickly and to see them through with a full suite of native capabilities, including: randomization, trial supply management, adjudication, ePRO, payments, DICOM Imaging, and eConsent. All backed by a highly tenured and experienced support team, ensuring quality, compliance and easy onboarding of the entire research team and clinical trials sites.
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MATLAB is a high-level programming and numeric computing environment widely utilized by engineers and scientists for data analysis, algorithm development, and system modeling. It offers a desktop environment optimized for iterative analysis and design processes, coupled with a programming language that directly expresses matrix and array mathematics. The Live Editor feature enables users to create scripts that integrate code, output, and formatted text within an executable notebook. Key Features and Functionality: - Data Analysis: Tools for exploring, modeling, and analyzing data. - Graphics: Functions for visualizing and exploring data through various plots and charts. - Programming: Capabilities to create scripts, functions, and classes for customized workflows. - App Building: Facilities to develop desktop and web applications. - External Language Interfaces: Integration with languages such as Python, C/C++, Fortran, and Java. - Hardware Connectivity: Support for connecting MATLAB to various hardware platforms. - Parallel Computing: Ability to perform large-scale computations and parallelize simulations using multicore desktops, GPUs, clusters, and cloud resources. - Deployment: Options to share MATLAB programs and deploy them to enterprise applications, embedded devices, and cloud environments. Primary Value and User Solutions: MATLAB streamlines complex mathematical computations and data analysis tasks, enabling users to develop algorithms and models efficiently. Its comprehensive toolboxes and interactive apps facilitate rapid prototyping and iterative design, reducing development time. The platform's scalability allows for seamless transition from research to production, supporting deployment on various systems without extensive code modifications. By integrating with multiple programming languages and hardware platforms, MATLAB provides a versatile environment that addresses the diverse needs of engineers and scientists across industries.
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AmpleLogic’s Stability Management Software is a comprehensive cGMP software designed to satisfy the demands of biotech, life sciences, pharmaceutical stability testing programs, and stability management. This Stability Management Software helps to simplify and test their organization’s operations and also specify the testing parameters for stability investigations
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Life Sciences companies include Pharmaceutical, Contract Development and Manufacturing Organization (CDMO), Biotechnology, Contract Research Organization (CRO) and Biosimilars continue to operate in a highly competitive environment. The Quality Control (QC) laboratory in a pharmaceutical company plays a critical role in the testing of Raw Materials, Stability, In-process and FG Samples. QC Analysts from different sections analyze incoming samples of different kinds. These include Finished Goods (FG), in-process products, stability samples, and environmental samples. Analysts may also be required to analyze raw materials. In organizations with diversified drug products, the number of samples to be tested per week will range from 150 – 400 Samples and each sample must go through a minimum of 6 tests. In such a scenario it is a challenge to prioritize the samples and assign equipment like HPLC/GC to the QC Analyst manually. HOD’s of QC Labs are under steady pressure to improve the lab operations in order to meet the Sample TAT (Turn Around Time). The equipment used in the Pharmaceutical and Biotech product testing are highly sophisticated, extremely sensitive, and very expensive. Maximizing both staff (Laboratory technicians and managers) time and machine time is essential in the QC lab to address the problems of varying demands and to maximize resource efficiency. Consequently, Planners/Managers are finding a way to move towards lean QC lab by improving their processes, improving effective utilization of resources, reducing lead times, and at the same time, increasing reliability by accelerating authorization processes for compliance. This affects both production and batch release. A good Quality Control Planning describes how an organization will achieve its quality goals by specifying the quality assurance and control activities which are performed as part of daily lab operations
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AIIR Consulting is a global executive coaching and leadership development firm that works with both mid-enterprise and Fortune 1000 companies around the world. AIIR's solutions leverage a proven, science-based coaching methodology, a bench of more than 200 certified executive coaches and consultants with both expertise in the behavioral sciences and real executive experience, and cutting-edge coaching technology and AI to increase the performance of leaders, teams, and organizations.
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Cognitus offers SAP certified solutions for transitioning to S4/HANA for a fixed price, scope and time including industry focused solution for Aerospace and Defense, Life Sciences and requirement focused solutions like Talent Management and CPQ Management. Cognitus also offers Hamilton, a proprietary product for IFRS 15 and 16 compliance that integrates as a SAP add-on.
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Edgile's Automated Regulatory Compliance for Pharmaceutical Life Sciences is a comprehensive solution designed to streamline compliance management within the pharmaceutical industry. By integrating with ServiceNow's Integrated Risk Management platform, ArC delivers over 850 harmonized laws, regulations, and industry standards, automatically updating them to ensure organizations remain current with evolving compliance requirements. Key Features and Functionality: - Extensive Regulatory Content: Provides access to a vast library of harmonized laws, regulations, and standards specific to the pharmaceutical sector. - Automated Updates: Delivers quarterly updates, incorporating new and amended regulatory content to maintain compliance readiness. - Regulatory Change Management: Includes a built-in application that identifies necessary changes to policies, standards, and controls, facilitating a closed-loop process for compliance management. - Seamless Integration: Natively integrates with ServiceNow IRM, enabling efficient management of compliance data within existing workflows. Primary Value and Problem Solved: ArC addresses the challenge of keeping pace with the dynamic regulatory landscape in the pharmaceutical industry. By automating the tracking and implementation of regulatory changes, it reduces the risk of non-compliance, enhances operational efficiency, and allows organizations to proactively manage their compliance posture. This proactive approach minimizes potential legal and financial repercussions associated with regulatory violations.
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SAP Batch Release Hub for Life Sciences solution enables life sciences companies to make data-based batch release decisions with lean, efficient, and streamlined processes, leading to reduced effort and risk in complying with life sciences regulations.
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VoxSciences for Offices converts the voicemails left on your office phone into text and delivers them to you as an email or SMS text message.
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No Code Data Science in your browser
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Cyber Science 3D, formerly operating under the name Viz-Tek, specializes in the design and development of virtual, augmented, and mixed reality systems and simulations.
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Quill is an intelligent automation platform that allows enterprise organizations to transform reporting workflows with natural language generation (NLG).
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Devōt is a software development company working on web and mobile applications, based in Zagreb, Croatia. We strive to keep interesting clients, but also to use our in-house knowledge, experience, and vision to create our internal products. Our story started with a few people who worked together long before the idea of Devōt. Sharing the same approach and values, our core team grew organically, evolving into a successful software company. Yet, we are not about uncontrollable growth, big people rotation, and body leasing. We are creating something a bit different and that is why we focus on people and quality. Our products are being used in various industries across the globe. Yet custom software solutions seem to be our forte. We take pride in developing the perfect fit for each client. Using our broad experience in technology, engineering, and social sciences, our goal is to create unique solutions that will save your time and money. We’re proud of our problem-solving skills and bringing something new to our clients and the market through our work. We are specialized in the services of consulting, software development, process automation, and service design. We are devoted to our job and aware that the quality work that we output is the result of a happy and productive team. We provide a calm working environment with an emphasis on building knowledge and investing in people.
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Low-code, FAIR Data Platform to * Fast-track drug discovery * Speed up drug safety reviews * Reuse existing data and knowledge & generate continuous knowledge * Streamline processes from R&D to manufacturing * Align strategic efforts*
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Keacyte is a software company delivering specialized SaaS solutions for the life sciences sector, with a focus on pharmaceutical, biotech, and medical device companies. Its platform empowers pharma commercialization through tools for CRM, field force automation, regulated content management, and compliance tracking. Key products like Keacyte DCR and Keacyte Expense streamline daily call reporting and expense management, enhancing operational efficiency and ensuring compliance.
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In addition to our open-source data science software, RStudio produces RStudio Team, a unique, modular platform of enterprise-ready professional software products that enable teams to adopt R, Python, and other open-source data science software at scale.
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The Anaconda Core is a unified platform for organizations looking to securely leverage open source for AI development. As the only comprehensive platform that combines trusted distribution, simplified workflows, real-time insights, and governance controls, the Anaconda Core helps organizations boost practitioner productivity while reducing time, cost, and risk.
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Transform, analyze and report on clinical trial data. Develop new therapies faster by giving everyone access to powerful pharma analytics.
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FreezerPro is an intuitive, fast, reliable and secure Web-based application that has a visually appealing interface which enables users to know precisely where a frozen sample is located even before opening the freezer door.
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Merit for Life Science-Operations advances the finance and operations (ERP) capabilities of Microsoft Dynamics 365 to deliver an industry-tailored solution that meets the rigorous requirements of pharma, biotech, and medical device organizations, including quality, procurement, materials management, production, and compliance. With Merit for Life Science, product owners and regulated manufacturers can drive increased process efficiencies, ready for and support rapid growth, and drive valuation while maintaining FDA CFR 21 part 11, EMA Annex 11, and other country-specific regulatory compliance. With Merit Solutions’ experienced implementation and consulting team, you gain a solution partner who understands the complex operational, manufacturing, and compliance challenges life science organizations face and has a demonstrated track record for supporting a successful digital transformation for product owners and manufacturing organizations including CMOs and CDMOs.