AmpleLogic eBMR Alternatives

MRPeasy helps small manufacturers grow with easy-to-use tools that cover all the essentials they need to manage their production. Having built the first cloud-based MRP platform in 2014, we offer user-friendly software-as-a-service that covers everything from production planning to CRM, skipping all the features that are too complex or irrelevant for small manufacturers. This means smaller manufacturers get access to powerful production planning tools, levelling the playing field with larger competitors. With MRPeasy, you know exactly how much your products cost and when they’re ready, helping you to steer your business effectively. MRPeasy integrates with leading accounting software like QuickBooks and Xero and e-commerce platforms like Shopify and WooCommerce, providing a comprehensive, fully integrated business management solution.

SimplerQMS offers a cloud-based Quality Management Software that is fully validated according to GAMP5 and specifically designed for the Life Science industry. This comprehensive QMS platform helps ensure compliance with various regulatory requirements, including FDA 21 CFR Part 11, EU Annex 11, GxP, cGMP, GAMP 5, GDPR, EU IVDR & EU MDR, ISO 13485:2016, 21 CFR Part 820, ICH Q10, and others. The software offers a wide range of Life Science QMS modules, such as Document Control, Change Management, Training Management, Supplier Management, Complaints Management, Non-Conformance and Deviation Management, CAPA Management, Audit Management, Technical Documentation Management, Risk Management, Quality KPIs, among others, ensuring a seamless experience. SimplerQMS enhances document handling by allowing users to work directly in Microsoft Office applications like Word, PowerPoint, and Excel.

Qualityze is a leading provider of enterprise quality management solutions, utilizing the Salesforce.com Technology Platform to build our EQMS Software solutions. Our team is 100% devoted to quality processes, compliance, and regulatory guidelines to address our customers' business environments. We do not distract ourselves with custom work or quality concerns. The idea of helping our customers create a culture of quality is not a new concept, but the way we developed our application, Quality Management Software, based on making it easy to use, intuitive, and inclusive. Therefore, the entire organization is involved in quality, not because they are told they should, but because it's easy, fun, and has a logical flow. We strive to optimize quality with excellence through our exclusive range of smarter quality management software solutions.

QT9's comprehensive cloud-based quality management software platform enables you to access real-time analytics in one unified suite. QT9 QMS makes it easy to automate ISO & FDA Compliance with 21 CFR Part 11 Electronic Approvals. Optimize processes for Document Control, CAPA's, Audits & More in one unified platform. Centralize records across multiple sites with ease. Never miss a deadline with automated email alerts/reminders. QT9 QMS makes quality management easy. Digitally transform Life Sciences, Biotechnology, Medical Device Manufacturers, Pharma, Aerospace and Food companies with user-friendly web portals for unlimited scalability. Get a free product tour! Start a Free Trial. Visit QT9qms.com

Mar-Kov is a leading provider of cost-effective software solutions for the pharmaceutical, chemical, cosmetics, flavors and fragrance, paints and coatings, and food industries. Delivering robust traceability solutions for process, batch, and formulation-based manufacturers, Mar-Kov helps businesses automate daily routine processes and streamline their operations while adhering to requirements of the HACCP, FDA, and other regulatory requirements. The solution also promotes paperless inventory by leveraging barcoding and an electronic batch recording system.

Qualio is an all-in-one quality and compliance management platform built for small and growing businesses in life sciences and healthcare. Reliable, affordable, and easy to use, Qualio helps companies building life saving products get to market faster by reaching 100% ISO, GxP, and FDA compliance. With Qualio, companies can conveniently manage document control, training, CAPAs, NCRs, audits, suppliers, complaints, and more in one platform.

Bringing breakthrough products to market in highly regulated industries can feel like an endless series of trade-offs. MasterControl's software simplifies GxP workflows so you never have to sacrifice quality for cost or innovation for regulation. Complete and connected meets fast and flexible. From quality event management to document control and integrated training - MasterControl Quality Excellence transforms your quality data and processes into a competitive advantage. Modernizing your manufacturing operations starts with modern software. From work orders to work instructions and production records (EBR or eDHR) to logbooks, MasterControl Manufacturing Excellence is the simplest way to digitalize manufacturing.

In pharmaceutical manufacturing, recording shop floor activities in real-time are essential to ensure quality and compliance with 21 CFR Part 11 and GMPs. An automated system ensures that batch records are error-free and retrievable and the batch manufacturing processes are trackable. EBR software like CaliberBRM eliminates paper-based processes and risks associated with them to ensure data integrity and product quality. In life sciences and highly regulated industries, real-time entry recording of 4Ms is inevitable. It enhances the business process. You can save a lot of time and effort by digitalizing batch production records. Electronic Batch Record (EBR) System gives you complete control of the 4Ms. CaliberBRM reduces inventory wastage, checks and aligns manpower as per need, deals with instrument management, reduces review cycle time, etc. It in turn reduces operating costs. Quality Review Management (QRM) stresses performing review by exception to accelerate batch release.

POMS's continual investments in MES Research and Development results in an MES solution that is flexible, easy to learn, and does not require customization. In fact, none of our customers use a customized solution today! POMSnet Aquila is a web-based manufacturing execution system (MES) crafted for Life Sciences manufacturing. Created using Microsoft .NET technology & HTML5, POMSnet is 100% web-based providing customers with an easy-to-learn interface that can be deployed and maintained cost effectively. POMSnet Aquila includes recipe and specification management, materials management, equipment management, production order management, recipe execution, electronic batch records, and device history. POMSnet implements best practices and business logic for Pharmaceutical Manufacturing Execution Systems.

With Opcenter Execution Pharma (formerly known as "SIMATIC IT eBR"), Siemens Digital Industries Software has developed a dedicated MES solution for the pharmaceutical industry that enables complete paperless manufacturing and full electronic batch recording. Opcenter Execution Pharma provides advanced features for designing, streamlining and managing production operations and processes, both manual and automated, via seamless integration between the MES, automation and enterprise resource planning (ERP) systems. Opcenter Execution Pharma ensures efficient manufacturing through consolidating and optimizing the number of different manufacturing resources available, including equipment, people, processes and products. It provides real-time production execution as well as availability and analysis of process and quality information to help optimize production activities from order creation to finished goods.

Arena’s product-centric quality management system (QMS) software enables medical device manufacturers to deliver safe and compliant products to market fast. Arena QMS streamlines new product development and introduction (NPDI) by connecting quality and product processes. Arena QMS ensures regulatory compliance to quality standards and regulations including FDA 21 CFR Part 820, Part 11 and ISO 13485. Arena QMS enhances visibility and traceability by controlling quality processes in context with bills of materials (BOMs), SOPs, DMRs, DHFs, specifications, drawings, and training plans.

Purpose-built for Pharma and other GxP-regulated companies to digitize production, quality, and compliance for manufacturing operations. Let the data do the talking. Teams take actions from real-time event monitoring into performance, track and solve quality issues as they happen. Give operators a tool that's easy to use and helps them get it right first time. Manufacturing is a complex business, add in GMP regulations and it gets significantly more so. Providing your teams the right tools is an opportunity to solve significant problems and realise transformational improvement. Vastly reduce time and effort for batch review and approval through review-by-exception, no more reviewing entire batch records. Automate wasteful activities like manually inputting and verifying data, moving paper records around the shop floor, performing and checking calculations, workflow management and more.

If you’re relying on multiple software and/or paper-based solutions to manage your compliance and manufacturing process needs, InstantGMP™ could be the key that unlocks the next level of success for your business potential. Seamlessly maximize production uptime, improve batch quality and meet all FDA compliance needs—and more—all with an affordable, paperless, all-in-one software solution. InstantGMP™ products work individually and together based on your business needs to deliver comprehensive, integrated software solutions that ensure end-to-end quality, consistency and GMP compliance. We’ll help you pick the right solution set for your business needs today, and tomorrow. Organize, manage and document batches electronically while reinforcing good manufacturing practices. Inventory Management Solution that meets Part 11 and GMP requirements. Complete quality system that comes with SOPs, templates and guided workflows - ideal for virtual biotech.

Laurel MES, is a browser-based and cloud-ready platform that has been designed by production engineers to ease operational difficulties in production lines/manufacturing facilities and for error-free batch production every time. A platform to drive, assign, manage and monitor all manufacturing activities from one dashboard. Laurel MES covers the complete manufacturing lifecycle from commercial production to final packaging. Compatible with all types of Pharma & Chemical Product Manufacturing. Laurel MES conceptualized and created by production engineers offers value-generating and error-reducing integrated solutions for all types of production lines in Pharma & Chemical domains. We have created a system that can be configured to completely replace your manual batch records with an electronic batch record that looks exactly like your physical Manufacturing record.

All-In-One ERP platform with unlimited scalability. QT9 ERP gives you a fully-integrated solution with real-time visibility. Includes 18+ modules for Bill of Materials, Accounting, Sales Orders, Shipping, Invoicing, Inventory Control, Purchasing, Job Scheduling, Shop Floor Manager & more. Digitally transform workflows with FDA 21 CFR Part 11 electronic signatures, electronic batch records, design history records, email reminders & dashboard views. Includes lot & serial number traceability. Digitize your workflows, simplify traceability & protect against recalls. Integrate all your organization's departments and functions into a single global ERP software. Get a free product tour! Start a Free 30-Day Trial. Visit QT9erp.com

Greenlight Guru’s Medical Device Success Platform is the only all-in-one solution that helps you get your products to market faster, with less risk, and advance your success in-market. The platform helps companies manufacture safer products and get to market faster, simplifies regulatory compliance, and provides a single source of truth by connecting the management of all product development, regulatory, and quality processes from documentation and design controls to submission and ongoing compliance. Device makers across the globe are replacing reactive quality management tools and shifting their focus and efforts to ensure successful product launches and in-market success of innovative, life-changing devices.

AmpleLogic’s Learning Management System (LMS) is designed to organize and monitor a vast number of GMP and Non-GMP training for life sciences, pharmaceutical manufacturing, API (Active Pharmaceutical Ingredient) Manufacturers, contract development and manufacturing organization (CDMO) biotechnology, and contract research organizations (CROs), including SOP, technical, HR, external, and research training. AmpleLogic Pharmaceutical Training Management Software aids in determining training requirements depending on a user’s Role. It’s also possible to create a department-specific training calendar, carry out and assess various forms of employee training programs, guarantee compliance through appropriate tracking, and keep training records annually with the creation of reports for management review.

AmpleLogic EDMS Software is a power-packed electronic document management system exclusively designed for Pharmaceutical and Biotech companies, developed, and implemented exclusively to meet the cGMP needs of Pharma domain with 21CFR Part 11 compliance, EU Annex 11 compliance can easily eliminate all the challenges faced by different companies AmpleLogic EDMS is a paperless document management system enables you to experience the effortless handling of all the documents and information. Various activities like document creation, review, approval, editing, document comparison, version control, parallel reviews are part of AmpleLogic Document Management System.

Empowering pharma companies and CDMOs to scale manufacturing while addressing supply chain bottlenecks, complex raw materials, and increasing development costs. Leverage the predictive power of AI and machine learning with the industry's leading manufacturing cloud. Always in a compliant manner. Collect and integrate real-time and historical data in a GxP-compliant manner from multiple sources, turning it into actionable insights. Leverage artificial intelligence (AI) and machine learning to find patterns that may lead to deviations and fix them before they become problems. The Aizon platform uses real real-time data capture from disparate data sources and predictive models to optimize pharma manufacturing processes. The Aizon platform performs GxP-compliant data acquisition, storage, and consumption making audits easier. Aizon works with international regulatory bodies to make sure AI algorithms can be qualified.

DeltaV S-series Electronic Marshalling with CHARMs lets you land field cabling wherever you want, regardless of signal type or control strategy. The DeltaV™ Distributed Control System (DCS) is an easy-to-use automation system that simplifies operational complexity and lowers project risk. The state-of-the-art suite of products and services increases plant performance with intelligent control that is easy to operate and maintain. The DeltaV DCS adapts to meet your needs, scaling easily without adding complexity. The inherent integration of the DeltaV system extends to batch, advanced control, change management, engineering tools, diagnostics, and more.

Azumuta assists manufacturing companies with driving performance by enabling factory workers to learn, solve issues and offer information progressively on the factory floor. Our software connects operators, supervisors and managers to every single manufacturing aspect, and supports a culture of constant improvement. Azumuta is a modular online platform that helps people in a factory environment to increase productivity and quality of production by better communication and technological support.

AmpleLogic Regulatory Information Tracker is built on the LOW CODE AND NO CODE (LCNC) PLATFORM and comprises two modules: ANDA and DMF Tracker. This Pharmaceutical RIMS Software can help you improve the quality of your data, boost operational efficiency, decrease mistakes, and streamline communication across departments.

‍Put power in the hands of your team. With intuitive, no-code procedure and recipe authoring designed for process scientists and process engineers, your teams can configure Tempo without code.‍ ‍Tempo allows users from your organization – or even across CDMO and their customers – to author recipes together in real time with live group-editing collaboration tools.‍ ‍Users can quickly create intelligent workflows with advanced capabilities like parallel execution, branching, and enforcement logic, as well as integrate referenceable parameters, formulas, equipment, materials, and operator actions, without a single line of code.‍ ‍Any user can also add augmented guidance – photos, videos, and AR overlays– to any step of a procedure. ‍Our native mobile app and hands-free, voice-enabled headset move with you. Tempo is optimized for use in all environments – the suite, cleanrooms, and while wearing PPE.‍

Tulip's flexible, no-code frontline operations platform helps manufacturers create front-end applications that guide operators, collect data from workers, machines, and devices, and track metrics against your KPIs. With Tulip, companies can digitally transform their operations in days, gaining real-time visibility of their operations to increase productivity, reduce errors, and drive continuous improvement.

Standardized process for managing investigational agents to improve patient safety while maintaining regulatory compliance. Safeguards to prevent the selection of expired or quarantined agents when dispensing. Reduce the risk of dispensing to patients not enrolled in a study. Capture complete dispense details and record them in the DARF. Prevent the dispensing of drugs that will expire within the prescribed treatment period by evaluating the dispense date, supply amount, and expiration date. Track dispense details including drug thaw time, time of reconstitution, and temperature reading at the time of reconstitution​. Centralized electronic management of investigational agents offers improved legibility, reduced paperwork/handwriting, and streamlined inventory management to provide pharmacists more time for valuable work and patient care. DARFs can be customized using filters yet still maintain a standard appearance for all protocols regardless of sponsor.

Organizational business complexity is rising. The lifetime of apps is decreasing. Address the business issue, collect data, and discard the solution once the issue has been resolved. Low Code No Code (LCNC) Application Development Platforms enable this in today’s environment. The AmpleLogic Low-Code and No-Code (LCNC) Development Platform includes a drag-and-drop form designer. It is a workflow that connects the people and processes within your organization to those outside of it. With the assistance of a LCNC Platform such as AmpleLogic, you may more effectively handle your organization’s particular requirements and close gaps across your business processes.

Mareana is a cloud-based Enterprise AI platform that connects siloed manufacturing data and enables real-time contextualization, processing, and predictive analytics to drive insightful business decisions. Mareana Manufacturing Intelligence helps small, medium, and large-scale enterprises improve yield, unlock capital and comply with regulatory mandates. Key Benefits with Mareana Intelligence Platform: - Connect all your Data in One Place like Paper batch records, CMO Process data, and Unstructured data - Create Product Genealogy in Real-Time and get Granular Product details, Process Anomalies & Variations, and New Data Impact Analytics - Unlock Capital by releasing On Hold Batches, Improving yield, and reducing Up-stream/Down-stream Non-Conformances - Execute Compliance Filings Flawlessly by ensuring complete reporting, leveraging all data sources, and reducing errors in filings 3 out of the top 10 pharmaceutical companies in the US are using Mareana's Platform for CPV & CMC.

Orbit Pharmaceutical Suite is an online cloud based business management solution that is built on the powerful platform of Oracle for the Pharmaceutical Manufacturers. It is single integrated software for all departments which includes Admin, Raw Material Store, Production, Accounts, Quality Control, Human Resource, Sales, Marketing, Distribution and IT department. It reduces operational costs and saves time. It enables better decision-making: managers have visibility to real-time & accurate information (integration of all data into a common framework), Extensive reporting, workflow and online real-time capabilities, Increased Operational Effectiveness & Productivity, Timely and target information feedback system for decision support, Improved Customer Support and Improved batch tracking management The solution has evolved over a period of 10 years of working with various Pharmaceutical business models and a proven track record of successfully delivering ERP projects on-time.

L7 Enterprise Science Platform (L7|ESP®) is a unified platform that contextualizes data and eliminates business silos via process orchestration. It's a comprehensive solution that facilitates the digitalization of data and scientific processes in life sciences organizations. L7|ESP has native applications, including L7 LIMS, L7 Notebooks, L7 MES, L7 Scheduling, and more. It can integrate with existing third-party applications, lab instruments, and devices to capture all data in a single data model. It has a low-code/no-code workflow designer and hundreds of pre-built connectors to enable rapid time-to-value and end-to-end automation. By leveraging a single data model, L7|ESP enables advanced bioinformatics, AI, and ML to offer novel scientific and operational insights. L7|ESP addresses data and lab management needs in life sciences, particularly in: ● Research and Diagnostics ● Pharma and CDMO ● Clinical Sample Management Resource Center: l7informatics dot com/resource-center

AmpleLogic's Quality Management Software (eQMS) is intricately crafted to meet the rigorous requirements of heavily regulated industries. The ISO 9001 certified cloud-based Quality Management System (QMS) is ideal for Lifesciences, Food & Beverages (F&B), Cosmetics, Medical Devices, Gene Therapy, and analogous sectors. As businesses acknowledge the challenges associated with manual quality checks—prone to both laborious efforts and errors—they are increasingly adopting QMS software solutions. These systems play a pivotal role in enhancing audit quality through process automation, efficient data management, and seamless API integration.

With PAS-X, Werum offers a mature standard software product for the highly regulated and batch-oriented process industries. The PAS-X MES provides out-of-the-box maximum standard functionality for all applications in the pharmaceutical and biopharmaceutical sector. Companies using PAS-X benefit from lean production and operational excellence. PAS-X provides all major functionalities required for efficient pharmaceutical and biopharmaceutical manufacturing out of the box. Werum PAS-X software product meets all requirements set forth by the approving authorities, such as the FDA. The great number of PAS-X standard interfaces accelerates implementation projects and ensures seamless information exchange with all surrounding IT and production systems. The PAS-X MES supports all major pharmaceutical industry segments, e.g. for vaccines, biopharmaceuticals, solids, liquids and other manufacturing operations.

Nova-LIMS has enabled laboratories to cut back manual and time-consuming activities and has empowered pharmaceutical and biotechnology organizations to achieve objectives such as decreasing product time to market while ensuring regulatory compliance. Over the years, the importance of system integration and automation has drastically increased, thus placing Nova-LIMS at the forefront of process harmonization and data centralization. Nova-LIMS allows for accountability and reliability between inter-related and interdependent departments. It provides the entire organization and their respective customers’ seamless integration between laboratory testing, scheduling, data collection, and real-time reporting. Unique to Nova-LIMS is the interface for seamless communication between LIMS and Quality Management Systems. Nova-LIMS, an out-of-the-box Laboratory Information Management software solution that is easily tailored to meet your specific requirements.

Drive study efficiency, regulatory compliance, and patient safety with Alpha Clinical Systems' electronic drug inventory management system (DIMS). Reduce site errors and workload while gaining real-time transparency. A comprehensive web-based system, ez-DIMS streamlines drug and device distributions at the site to eliminate transcription errors. Integrated with ex-SourceDocx, automatically accounts for supply disbursements, providing real-time visibility of drug inventory. Replace slow, error-prone, manual processes with user-friendly ez-DIMS. Reduce site workload with user-friendly scanners to quickly, easily, and accurately record study supply inventory and accountability at the patient, site, and study levels. Drug inventory violations at the site are the second most common regulatory inspection finding. Reduce medication assignment/dispensation errors by leveraging QC cross-checks between ez-DIMS and ez-SourceDocx.

Affytrac is our secure EHS software for the life science industry, currently in use at biotechnology, pharmaceutical and medical device companies throughout the world. As a web-based tool, there's no software to install, and with our streamlined setup process, there are no delays in having your EHS program automated, optimally tuned, and always at your fingertips. Simple and intuitive to use, yet powerful and full-featured, Affytrac includes all the functionality you expect in EHS software, without any unnecessary complexity to get in your way. Task Management lets you define your organization's set of compliance and safety tasks. Assign to personnel, add your target dates, and Affytrac automatically notifies staff and tracks progress. Document and track Corrective Actions identified through accidents, incidents, safety committees, regulatory inspections, and risk assessments.

Cosmetic Factory is a PLM SaaS, all-in-one and modular for brands, manufacturers and distributors in the cosmetics industry. It covers all the functional dimensions necessary for the creation, management and international marketing of cosmetic products. From the marketing brief to the global commercialization, including R&D, formulation, testing, international compliance, pilot batches, packaging or labels, Cosmetic Factory offers expert support at each stage of development and allows your different departments to collaborate, notably with its integrated PMS. Among the key features, the Formula Check, which is based on Artificial Intelligence, indicates whether a formula is compliant with regulations on one or more markets by analyzing the formula but also the product typology and the target. Its formulation cycle module guarantees time savings in the development of new products, with its advanced raw material comparator, real-time regulatory compliance calculation, etc.

RxConnect is a web-based pharmacy solution specifically designed to meet the medication dispensing needs of inpatient hospitals. Its easy-to-use interface allows clinicians to send pharmacy orders directly within their EHR, electronically connecting order entry with pharmacies to seamlessly receive and provide medication. RxConnect supports dispensing capabilities with automated dispensing machines (ADMs) and connects with the electronic medication administration record (eMAR) to provide closed-loop medication management. Clinicians can review and manage drug interactions, allergies and patient-specific dosing via a clinical rules engine. Drug disease, alcohol interactions as well as lab and tobacco, pregnancy, lactation and general precautions and black box warnings are also provided. Inventory, formulary, progress notes, labs integration and intervention documentation, as well as pharmacy notes, are all included.

Drive productivity, ensure compliance, streamline processes, and improve organizational efficiency by using the world's most widely deployed LIMS (Laboratory Information Management System). Thermo Scientific™ SampleManager LIMS™ delivers laboratory management, data management, (SDMS) and process execution/procedural ELN (LES) capabilities in a single solution. Laboratories across all industries, including pharmaceutical, food and beverage, oil and gas, petrochemical, water and environmental, manufacturing and contract testing rely on SampleManager LIMS to unlock the power of their laboratory data.

Designed as a factory wide ingredient control & traceability solution for manufacturing companies of all sizes. V5 is an excellent plugin to existing ERP/Accounting Software, or it can run stand alone. V5 offers a speedy return on investment. Hundreds of configuration options exist in the standard product, enabling each system to be setup to handle many manufacturing execution applications. Supported industries include food and beverage, chemical & plastics, pharmaceutical & life sciences. V5 Formula Control Scale System is the perfect way to ensure ingredients are measured & traced accurately and consistently, without costly giveaway or out-of-specification batches. The system ensures each weighed ingredient has enforced +/- unique tolerances, preventing recipe completion until all ingredients are weighed using the green speedometer style target zone.

Heightened variability, rampant product proliferation, and limited supply chain visibility — all pose serious headaches for high-mix manufacturers. Despite these challenges, executives must find ways to improve efficiency, meeting demand while exceeding customer expectations. That’s why leading pharmaceutical, consumer goods, food, beverage, and other manufacturers rely on Flowlytics® to continuously align demand, supply and capacity while ensuring regulatory compliance. The Flowlytics suite was developed to take into account supply and demand variability and enables a true flow-based approach to manufacturing – one that aligns your processes around a value stream and support sustainable performance improvement initiatives. Optimize inventory levels, lot sizes and rhythm wheels. Support any variation of pull manufacturing.

Our manufacturing solution consists of a production system that ensures orders, sales, and purchases are in harmony to ensure the lowest inventory possible. The software helps with planning and execution; alerts are triggered if execution doesn't match planning. Automotive Component automates your processes, ensures just-in-time inventory, reduces cost, and enables quality control. You achieve improved operational efficiencies, better control and transparency, and improved accountability. Fix your core processes before they put you in a fix. Pharmaceutical. Allows access to real-time information and visibility into demand cycles. It facilitates better planning and ensures improved compliance. Manufacturing Solution. Offers consulting-driven ERP implementation to overcome these challenges and accelerate business performance. Process manufacturers face dynamic industry challenges such as: Variations in bills of material (BoM). Complex inventory management processes.

Ensure the safety of your health system with a complete end-to-end solution for managing pharmaceutical recalls. Today, 60% of US hospitals use OneRecall™ to help reduce legal risk, improve patient safety, simplify regulatory reporting, and enhance the recall management process. Providers and suppliers join the OneRecall™ community to automate product alert distribution and electronically participate in remediation activities, saving time, money, and, most importantly, lives. It is critical to quickly communicate recall details to all affected stakeholders within the healthcare supply chain. We’re proud to offer OneRecall™, providing hospitals a comprehensive solution for the ever-growing challenge of managing manufacturer recalls. To learn more about these or other Inmar products or services, contact us. We’re happy to help. Aggregated and uniform recall notifications from a single provider. Reduced time from receipt of product notifications to recall resolution.

As a thought leader in compliance for the Life Sciences industry, THINQ provides compliance solutions to a broad range of pharmaceutical, medical device and biotechnology companies. With a special expertise in validation, THINQ is now leading the way in changing how validation is managed in Life Sciences companies. THINQ offers comprehensive compliance program development and management—powerful market-proven solutions, custom-tailored for our enterprise clients. Transform governmental mandates into a competitive advantage!In today’s regulatory environment, forward-thinking organizations understand that compliance, risk mitigation and validation must not only be managed but mastered. With more than 20 years of market-proven compliance expertise and experience, THINQ Compliance can show your enterprise how to create and implement a risk-management and compliance solution. Experience the thrill of compliance training classes delivered by some of the brightest minds in the industry.

Predisys develops quality control, test data management and manufacturing business intelligence solutions for companies seeking to optimize product quality and process efficiency, reduce the cost of compliance, and enhance manufacturing visibility across the product life cycle and supply chain. Its flagship solution, Predisys Analytical Suite, comprises of tools for collecting and managing quality and performance measurement data from multiple data sources for analysis and reporting, using powerful statistical process control (SPC) methods and robust statistical, analytical and data visualization tools. It is the ideal software for turning vast amounts of inspection and test data into actionable information. Predisys’ enterprise solution for medical device, diagnostics, biotech and pharmaceutical companies is FDA compliant and facilitates a cost-effective, flexible and surprisingly simple transition from paper-based records to a fully automated system for electronic management.

Develop and publish accessible content in digital, PDF, and print formats with our XML Professional Publisher. Built for the most demanding publishing environments, you can produce newsletters, books, magazines, loose-leaf manuals, catalogs, and electronic documents in more than 40 languages. Automate the composition and pagination of XML, or other structured content, to create high-quality output with a rapid turnaround. Maintain compliance with global regulatory accessibility standards and ensure equal access for all across your print, PDF, and ePub materials. With a streamlined process for the configuration of PDF tags, bookmarks, and annotations, you have the ability to publish multilingual, accessible documents to aid customers and users with access limitations globally.

For over 35 years Unisoft has been a leader providing innovative shop floor automation software to automate New Product Introduction (NPI). Unisoft provides automation software for lean manufacturing in industries such as electronics, medical, chemicals, aerospace, pharmaceuticals, foods, textiles and other manufacturing industries. Our software brings your products into production as fast as possible with the least amount of effort and at an affordable price. NPI has never been easier. The Unisoft OneFACTORY software suite is a complete solution to automate production floors in modern electronics and other manufacturing industries. Unisoft OneFACTORY software suite, is powerful yet easy to use and modular, purchase only the modules you require now. The Unisoft software imports all types of CAD, Gerber, XY rotation, BOM, etc. data formats which is key for PCB electronic contract manufacturers who have to without delay work with the variety of project data sources.

Customize and Scale Your Peer Review Process for Code and Documents With Collaborator. Collaborator is the premier peer code & document review tool for development teams that take software quality seriously. Comprehensive Review Capabilities – Review source code, design docs, requirements, user stories, test plans, and documentation in one tool. Proof of Review – Ensure proof with electronic signatures & detailed reports to meet regulatory compliance standards. Support for 11 SCMs, including Git, SVN, TFS, Perforce, CVS, ClearCase, RTC, & more. Integrations with GitHub, GitLab, Bitbucket, Jira, Eclipse, Visual Studio, & more. Real-Time Updates. Threaded chat shows conversations as well as highlights changes & defects for visibility during each code review. Each team and project has unique requirements. Why would the same type of review work for everything? With custom review templates and checklists in Collaborator, it is easy to build peer review frameworks.

BatchDialer is a powerful and comprehensive outbound dialer solution designed to drive efficiency and productivity for businesses. With features such as multi-line dialing, call recording & forwarding, IVR, and customizable agent scripts, BatchDialer empowers sales, marketing, and BPO teams to effectively reach their target audience and achieve their goals. The unique offerings of BatchDialer, such as phone number reputation monitoring, rapid fire dialing mode, property details in-view, and included phone numbers, provide businesses with a competitive edge. By streamlining campaign management, ensuring compliance with regulations, and providing valuable insights and tools, BatchDialer enables businesses to optimize their telecommunications efforts, maximize productivity, and drive meaningful connections with customers.

A pharmacy service must be your partner in reducing cost, enabling better clinical and financial outcomes, and improving staff productivity and satisfaction. A pharmacy service must be easy to do business with and a seamless part of your organization's operations. To that end, we provide Millennium pharmacy services for Care, Cost, and Compliance. Millennium replaces frustration, inefficiency, and waste with responsiveness, efficiency, and cost savings. We deliver on the promise of "the right drug, for the right patient, at the right time, for the right price" so you can deliver the best patient care while reducing costs, improving efficiency, and more easily meeting compliance demands. Only Millennium combines Just-In-Time Dispensing with electronic prescription ordering, formulary management, medication and treatment administration, and corresponding medical records.

Effective production management – anytime, anywhere. ENISCO’s modular manufacturing execution system (E-MES) offers end-to-end support for factory operations – both horizontally, across the entire manufacturing process, and vertically from ERP to shop floor IT. Integrated data capture, analysis and visualization ensure complete transparency, forming the basis for digital factory solutions in line with Germany’s Industry 4.0 initiative. E-MES is browser-based software that supports multiple operating systems. Users can access data at any time, anywhere in the world – no client software needs to be installed. On-site manufacturing staff and maintenance engineers, as well as other employees and decision-makers – near or far – can monitor and streamline production via tablets, smartphones or smartwatches. E-MES provides important information and insights – allowing users to critically review past manufacturing processes and make better decisions going forward.

With out-of-the-box applicability and checklist questions, Dakota Auditor helps organizations address local EHS compliance while synchronizing global audit and inspection programs. The auditor makes it easy to test each site's EHS compliance and safety status. Using Decision-Tree-Logic, Auditor guides users in identifying applicable regulatory requirements and audit checklists. Users can add custom questions to address internal policies and use tags to further refine audits. Leverage site-specific profiles to assess compliance with applicable regulations and conformance with management system requirements. Auditor’s structured regulatory database provides a consistent Knowledge Base for your teams, regardless of their Environment, Health, and Safety experience, helping to ensure quality reviews. From the Audit Gauge to Red Flag dashboards, Auditor provides EHS leaders and decision-makers with the insights they need.