Alternatives to anicomply

Qualio is a purpose-built quality and compliance platform for life sciences companies operating in complex, high-stakes regulatory environments. Medical device, SaMD, biotech, and pharma teams use Qualio to replace fragmented eQMS tools, spreadsheets, and consultant-driven audits with a single, validated system that delivers continuous audit and inspection readiness. Qualio combines a modern eQMS with Compliance Intelligence—an AI-driven layer that continuously evaluates how well real operating data aligns with regulatory requirements. Instead of treating audits as one-off events, teams gain always-on visibility into compliance coverage, risk exposure, and readiness across FDA, ISO, EU MDR, GxP, and software-intensive standards. Core quality workflows—document control, training, CAPA, change management, supplier quality, and design controls—are directly connected to regulatory obligations and objective evidence. Deep integrations with Jira, Azure DevOps, GitHub, TestRail, and Salesforce automatically capture proof from development and operational systems, eliminating manual evidence gathering and reducing compliance drag on engineering teams. Compliance Intelligence runs multi-standard gap analysis in under an hour, flags emerging risks before they become findings or 483s, and maps reusable evidence across frameworks to accelerate submissions and market expansion. All insights are explainable and traceable back to specific clauses and internal policies, supporting validation and audit expectations. The result: audit readiness in weeks instead of months, fewer fire drills, faster launches, and lower long-term compliance cost. Qualio turns compliance from a reactive burden into a predictable, scalable system.

The ultimate MRP solution for small manufacturers! MRPeasy offers an affordable, user-friendly, and cloud-based MRP system tailored specifically for small manufacturing businesses. Transform your customer orders into manufacturing orders and let the system schedule them automatically. It effortlessly books items from your inventory, and if needed, initiates purchase orders on your behalf. Depending on the real-time requirements, MRPeasy allows for both forward and backward scheduling. Automated checks ensure the availability of workers, workstations, and materials. Maintain a comprehensive overview of all your operations at all times! MRPeasy also smoothly integrates with premier accounting software such as QuickBooks and Xero, along with e-commerce platforms like Shopify and WooCommerce. This integration creates an all-encompassing business management solution that meets your every need.

Aizon: Intelligent GxP Manufacturing Aizon helps life sciences manufacturers modernize production with AI solutions designed for regulated GxP environments. By leveraging our platform, companies can minimize variability, maximize yield, and safeguard product quality at every stage of the process. - Aizon Execute — Intelligent Batch Record (iBR): Move from paper to digital records in a matter of weeks, cutting deviations and enabling faster batch release. - Aizon Unify — Contextualized Intelligent Lakehouse: Break down data silos by unifying and contextualizing information across plants and systems, turning raw data into actionable insight. - Aizon Predict — GxP AI Industrialization: Apply predictive intelligence to optimize process parameters, strengthen Right-First-Time performance, and drive higher output. With Aizon, pharmaceutical and biotech manufacturers can unlock operational intelligence—gaining clarity from historical data, visibility into the present, and foresight to steer the future of manufacturing.

Best-in-Market Speech-to-Text & Voice AI for Enterprises. Speechmatics delivers industry-leading Speech-to-Text and Voice AI for enterprises needing unrivaled accuracy, security, and flexibility. Our enterprise-grade APIs provide real-time and batch transcription with exceptional precision—across the widest range of languages, dialects, and accents. Powered by Foundational Speech Technology, Speechmatics supports mission-critical voice applications in media, contact centers, finance, healthcare, and more. With on-prem, cloud, and hybrid deployment, businesses maintain full control over data security while unlocking voice insights. Trusted by global leaders, Speechmatics is the top choice for best-in-class transcription and voice intelligence. 🔹 Unmatched Accuracy – Superior transcription across languages & accents 🔹 Flexible Deployment – Cloud, on-prem, and hybrid 🔹 Enterprise-Grade Security – Full data control 🔹 Real-Time & Batch Processing – Scalable transcription 🚀 Power your Speech-to-Text and Voice AI with Speechmatics today!

Qualityze delivers cloud-based Quality Management System (QMS) and Enterprise Quality Management Software (EQMS) solutions built natively on the Salesforce platform. Designed for regulated and compliance-driven industries, Qualityze centralizes and standardizes enterprise quality processes within a secure, scalable cloud environment. The platform supports CAPA management, audit management, document control, training management, change control, risk management, and supplier quality workflows through configurable automation and role-based governance. Real-time dashboards, advanced reporting, and end-to-end traceability provide full visibility across quality operations. Built to eliminate siloed systems and manual processes, Qualityze enables life sciences, manufacturing, and other regulated organizations to streamline compliance with global standards while improving operational efficiency and accountability. With seamless Salesforce integration and enterprise-grade scalability, Qualityze helps organizations modernize quality management, reduce compliance risk, and drive measurable continuous improvement across global teams.

SimplerQMS offers a cloud-based Quality Management Software, specifically designed for the Life Science industry. SimplerQMS 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, and ICH Q10, among others. The system is fully validated according to GAMP5. The system offers a range of Life Science QMS modules such as Document Control, Change Control, Training Management, Supplier Management, Complaints Management, Non-Conformance and Deviation Management, CAPA Management, Audit Management, Technical Documentation Management, Risk Management, Quality KPIs and more. SimplerQMS integrates with Microsoft Office and allows users to work with documents in applications such as Word, PowerPoint, and Excel. Overall, SimplerQMS delivers efficient, paperless workflows that align with the compliance requirements of the Life Science industry.

Mar-Kov is a leader in providing cost-effective software solutions to the pharmaceutical, chemical and cosmetics, flavors, fragrance, paints and coatings, as well as food industries. Mar-Kov provides robust traceability solutions to process, batch, or formulation-based manufacturers. This helps businesses automate their daily routines and streamline operations while complying with regulatory requirements such as HACCP, FDA, etc. This solution promotes paperless inventory through the use of barcoding and an electronic batch record system.

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

In the realm of pharmaceutical production, it is crucial to document activities on the shop floor in real-time to maintain quality standards and comply with regulations such as 21 CFR Part 11 and Good Manufacturing Practices (GMPs). Utilizing an automated system guarantees that batch records are free from errors and can be easily accessed, while also allowing for the tracking of batch manufacturing processes. Electronic Batch Record (EBR) software, such as CaliberBRM, replaces traditional paper-based systems, thereby mitigating associated risks and ensuring the integrity of data and product quality. In industries that are highly regulated, particularly in life sciences, the real-time recording of the 4Ms becomes a necessity as it streamlines business processes. Transitioning to digital batch production records can significantly reduce both time and effort. The EBR system provides comprehensive oversight of the 4Ms, enabling organizations to minimize inventory waste, optimize workforce allocation, manage instruments effectively, and shorten review cycles, all of which lead to decreased operational costs. Furthermore, Quality Review Management (QRM) emphasizes the importance of exception-based reviews to expedite batch releases, enhancing overall efficiency. By implementing these modern solutions, companies can create a more agile and responsive manufacturing environment.

It can seem like a never-ending series of tradeoffs to bring breakthrough products to market within highly regulated industries. MasterControl's GxP software simplifies workflows, so you don't have to compromise quality for cost or innovation with regulation. Complete and connected meets flexible and fast. MasterControl Quality Excellence transforms quality data and processes to a competitive edge. Modern software is the first step in modernizing your manufacturing operations. MasterControl Manufacturing Excellence, from work orders to production records (EBR/eDHR), to logbooks and work instructions, is the easiest way to digitalize manufacturing.

POMS consistently invests in research and development for its manufacturing execution system (MES), resulting in a solution that is adaptable, user-friendly, and does not necessitate any customization. Remarkably, all of our clients currently operate without any tailored solutions! POMSnet Aquila is a web-oriented MES specifically designed for the Life Sciences sector, built using Microsoft .NET and HTML5 technologies. The entirely web-based platform offers an intuitive interface that is both easy to learn and cost-effective to deploy and maintain. POMSnet Aquila encompasses a range of functionalities, including management of recipes and specifications, materials oversight, equipment tracking, production order control, recipe execution, electronic batch records, and device history. Moreover, POMSnet integrates industry best practices and business logic tailored for Pharmaceutical Manufacturing Execution Systems, ensuring optimal operational efficiency and compliance. By continually evolving its offerings, POMS demonstrates its commitment to meeting the dynamic needs of the Life Sciences industry.

AmpleLogic eBMR differentiates itself through its flexible modular architecture and user-friendly low-code platform, providing customized solutions specifically designed for the pharmaceutical and biotechnology sectors. It boasts features such as real-time data integration, dispensing modules, and electronic signatures, which collectively ensure adherence to international regulatory requirements. By automating quality control processes, AmpleLogic eBMR enhances productivity, reduces compliance expenses, and simplifies the batch review process. Its electronic record-keeping capabilities minimize errors, leading to more accurate decision-making outcomes. Additionally, the software accelerates product modifications, aligns with regulatory standards, and boosts overall efficiency in pharmaceutical manufacturing. It allows for detailed specifications of raw materials and precise weight-age calculations, thereby optimizing material management through accurate dispensing methods. Furthermore, the system streamlines the routing, reviewing, and approving of manufacturing records, contributing to a more efficient batch review process that ultimately drives productivity levels higher. This comprehensive approach not only meets industry demands but also positions businesses for sustained growth.

Empower your team by enabling them to take control of their processes. With user-friendly, no-code tools for procedure and recipe creation tailored for process scientists and engineers, your team can effortlessly configure Tempo without any coding expertise. Tempo facilitates real-time collaboration, allowing users from your company, as well as partners and customers from CDMO, to co-author recipes using live group-editing features. Users can swiftly design sophisticated workflows that incorporate advanced functionalities such as parallel execution, branching, and enforcement logic, along with the ability to integrate referenceable parameters, formulas, equipment, materials, and operator actions, all without writing any code. Additionally, any user can enhance procedures by incorporating augmented guidance, including photos, videos, and AR overlays, into any procedural step. Our mobile application and voice-activated headset are designed to accompany you wherever you go, ensuring usability in various settings – from suites and cleanrooms to environments where personal protective equipment is worn. This versatility allows teams to maintain productivity and efficiency, regardless of the circumstances.

Designed specifically for pharmaceutical and other GxP-compliant organizations, this solution streamlines the digitization of production, quality, and compliance processes within manufacturing operations. Empower your data to guide decisions effectively. With real-time event monitoring, teams can swiftly respond to performance issues and tackle quality challenges as they arise. Equip operators with a user-friendly tool that enhances their ability to achieve accuracy on the first attempt. Navigating the complexities of manufacturing is challenging, especially with the added layer of GMP regulations. By providing your teams with the appropriate resources, you can address critical issues and unlock transformative advancements. Significantly cut down on the time and effort needed for batch reviews and approvals through a review-by-exception approach, eliminating the need for exhaustive reviews of complete batch records. Furthermore, automate tedious tasks such as data input and verification, managing paper records across the production floor, carrying out and double-checking calculations, and overseeing workflows, among others. This not only enhances efficiency but also allows teams to focus on more strategic initiatives.

Siemens Digital Industries Software has introduced Opcenter Execution Pharma, previously referred to as "SIMATIC IT eBR," which is a specialized MES solution tailored for the pharmaceutical sector, facilitating entirely paperless production and comprehensive electronic batch recording. This innovative platform boasts sophisticated capabilities for designing, refining, and overseeing both manual and automated production activities, achieved through seamless integration with MES, automation, and enterprise resource planning (ERP) systems. By optimizing the utilization of various manufacturing resources—such as equipment, personnel, processes, and products—Opcenter Execution Pharma plays a crucial role in promoting efficient production. It delivers real-time insights into manufacturing execution along with access to process and quality information, thereby aiding in the enhancement of production workflows from the initial order stage to the final product. Ultimately, this solution not only improves operational efficiency but also supports compliance with stringent industry regulations.

InstantGMP™, which replaces multiple software and/or paper-based solutions for managing your manufacturing and compliance needs, could be the key to unlocking your business's full potential. With a single, affordable software solution, you can easily increase production uptime, improve batch quality, and meet all FDA compliance requirements. InstantGMP™, which can be used individually or together depending on your business needs, delivers comprehensive, integrated software solutions that ensure quality, consistency, and GMP compliance. We will help you choose the right solution for your business today and tomorrow. You can organize, manage, and document batches electronically while promoting good manufacturing practices. Inventory Management Software that meets Part 11 requirements and GMP requirements. A complete quality system with templates, SOPs and guided workflows that is ideal for virtual biotech.

Laurel MES is a cloud-based platform designed specifically by production engineers to streamline operations in manufacturing facilities, ensuring consistent and accurate batch production. This comprehensive system allows users to drive, assign, manage, and oversee all manufacturing processes from a single dashboard. Covering every stage of the manufacturing lifecycle—from initial production to final packaging—Laurel MES is compatible with various types of Pharma and Chemical Product Manufacturing. By offering integrated solutions that enhance value and minimize errors, Laurel MES effectively serves all production lines within the Pharma and Chemical sectors. The system has been designed to fully replace traditional manual batch records with electronic versions that mirror the appearance of physical manufacturing records, thus facilitating a smoother transition to digital documentation. This innovative approach not only boosts efficiency but also promotes better compliance with industry regulations.

The L7 Enterprise Science Platform (L7|ESP®) is a comprehensive platform designed to contextualize data and remove business silos through process orchestration. This all-in-one solution supports the digitalization of data and scientific processes within life sciences organizations. It includes native applications like L7 LIMS, L7 Notebooks, L7 MES, and L7 Scheduling. L7|ESP seamlessly integrates with third-party applications, lab instruments, and devices to consolidate all data into a unified model. Featuring a low-code/no-code workflow designer and numerous pre-built connectors, it ensures rapid implementation and full automation. Utilizing a single data model, L7|ESP enhances advanced bioinformatics, AI, and ML to provide new scientific and operational insights. L7|ESP addresses the data and lab management needs and challenges within the life sciences sector, specifically targeting: ● Research and Diagnostics ● Pharma and CDMO ● Clinical Sample Management Explore the L7 Resource Center for on-demand recordings, case studies, datasheets, and more: l7informatics dot com/resource-center

SG Systems Global offers traceability and manufacturing solutions for regulated and non-regulated industries, integrating with ERP and MES platforms to boost efficiency and ensure product quality. Key Modules: * Electronic Batch Records (EBRs): Digital records to meet 21 CFR Part 11 and GMP compliance, reducing manual errors. * Formula Control: Ensures accurate ingredient measurement and consistency across batches. * Batch Control: Tracks production in real time, enabling lot validation and recall management. * Warehouse Management System (WMS): Manages inventory with barcode scanning and real-time stock updates. * Production Scheduling: Automates workflows, assigns tasks, and generates performance reports. These solutions streamline processes, enhance compliance, and support scalable growth for manufacturers.

The DeltaV S-series Electronic Marshalling utilizing CHARMs allows for flexible placement of field cabling, independent of the type of signal or control methodology employed. The DeltaV™ Distributed Control System (DCS) is designed to streamline automation processes, which reduces operational challenges and mitigates project risks effectively. This advanced collection of products and services enhances plant efficiency through intuitive control solutions that are straightforward to manage and service. Importantly, the DeltaV DCS is adaptable, easily scaling to fit your specific requirements without introducing additional complexity. Furthermore, the seamless integration capabilities of the DeltaV system encompass various functions including batch processing, advanced control, change management, engineering tools, diagnostics, and much more, ensuring a comprehensive solution for your operational needs. Ultimately, this flexibility and integration pave the way for improved productivity and reliability in industrial environments.

Arena's quality management system (QMS) software, designed specifically for product-centric environments, empowers medical device manufacturers to efficiently bring safe and compliant products to the market. By integrating quality and product processes, Arena QMS simplifies the new product development and introduction (NPDI) process. It provides assurance of regulatory compliance with essential quality standards and regulations, such as FDA 21 CFR Part 820, Part 11, and ISO 13485. Furthermore, Arena QMS improves visibility and traceability by managing quality processes in conjunction with various essential documentation, including bills of materials (BOMs), standard operating procedures (SOPs), device master records (DMRs), design history files (DHFs), specifications, drawings, and training plans. This holistic approach not only facilitates compliance but also fosters a culture of quality throughout the organization.

QT9 ERP helps manufacturers in regulated industries simplify production, inventory, and compliance with one connected, validated platform. Seamlessly integrating with QT9 QMS, it delivers real-time visibility, end-to-end traceability, and automated FDA and ISO compliance. Available cloud-based or on-premise, QT9 ERP includes built-in validation, configurable workflows, and unlimited support to help teams reduce errors, boost efficiency, and stay audit-ready.

Tulip's flexible, non-code frontline operations platform allows manufacturers to create front-end apps that guide workers, collect data from machines and workers, and track metrics against your KPIs. Tulip allows companies to digitally transform their operations within days. They can gain real-time visibility into their operations to improve productivity, reduce errors and drive continuous improvement.

Azumuta is an all-in-one system to digitalize your shop floor operations. Become a paperless factory, save time in manual data entry, and prevent errors by creating and managing digital work instructions, audits, employee training, and quality management reports from a single platform.

Greenlight Guru is the only product development and quality management platform designed specifically for medical device companies. The Medical Device Success Platform helps companies get safer products to market faster, simplifies FDA and ISO regulatory compliance, and provides a single source of truth by connecting the management of all quality processes like CAPAs, risk, audits, document control, training, design control, and more. Device makers across the globe are replacing their outdated paper-based and general-purpose legacy quality systems with Greenlight Guru to push beyond baseline compliance and achieve True Quality.

The MODA Platform serves as an all-encompassing solution that integrates both manufacturing and lab data into a cohesive source, aimed at speeding up the release of pharmaceutical products while eliminating labor-intensive and error-prone workflows. Designed with a focus on user needs, the platform is modular and scalable, enabling organizations to initiate with a module that aligns with their immediate requirements and to expand as necessary. The primary modules include MODA-EM for Quality Control, which automates the entirety of QC processes; MODA-ES for Manufacturing, which allows for intuitive and flexible electronic batch records; and MODA eLogs for electronic documentation, which offers user-friendly digital logbooks that ensure compliance. Created specifically for the pharmaceutical sector, the platform addresses the challenges associated with traditional paper records, such as delays in approval cycles, inaccuracies in entries, and risky calculations, thus facilitating a smoother digital transformation. Furthermore, this innovative solution not only enhances efficiency but also promotes a culture of quality and compliance throughout the organization.

Sarjen’s Manufacturing Process Automation solution brings true digital transformation to the shop floor by embedding AI at the core of every operation. It is not just about replacing paper with screens; it is about enabling systems to think, learn, and continuously improve. AI captures real-time production data from machines, operators, and quality checkpoints, turning raw information into actionable intelligence. It detects deviations instantly, predicts potential failures before they disrupt production, and recommends corrective actions to prevent costly downtime. With intelligent pattern recognition, AI strengthens quality control by identifying anomalies that manual reviews often miss. It reduces human errors, streamlines batch execution, and ensures every step aligns with regulatory and compliance standards. Predictive analytics optimize resource utilization, improve yield, and balance workloads dynamically. Instead of reactive decision-making, teams gain proactive insights that drive faster, smarter responses. AI-powered automation also enhances traceability and transparency, creating a connected manufacturing ecosystem where data flows seamlessly across systems. This level of intelligence accelerates release cycles, improves operational efficiency, and builds resilience in highly regulated industries like pharmaceuticals and life sciences. By combining automation with advanced AI capabilities, organizations move beyond incremental improvements and achieve sustainable, scalable transformation in manufacturing performance.

Accevo Smart Factory (formerly ANT Solutions) is a next-generation Manufacturing Operations Management (MOM) platform built to help factories modernize and thrive in the Industry 4.0 era. Designed for end-to-end digital transformation, it connects production lines, machines, and people in a unified ecosystem. Its suite includes OEE performance monitoring, MES, CMMS, APS, QMS, and EMS, giving manufacturers full control of performance, planning, maintenance, and energy use. By digitizing workflows and eliminating manual reports, Accevo helps reduce downtime, increase efficiency, and deliver up to 15% higher OEE within weeks. The platform supports both cloud-native and on-premise deployments, ensuring security, scalability, and easy integration with ERP systems. AI-driven analytics and real-time dashboards empower teams to react 65% faster to production issues while cutting reporting time by 90%. Accevo’s proven implementation methodology guarantees measurable results in as little as six weeks. Backed by a team of industrial automation experts, Accevo transforms complex operations into streamlined, data-powered systems for global leaders in manufacturing.

Wherefour is an easy-to-use ERP system and food traceability software that allows you to use batch, track/trace and inventory control. It also allows you to manage recipe management, batch and unit costsing, supplier purchasing and more. Wherefour can be used on any device that has internet access.

FoodOps is a cloud-based platform for food manufacturing that transforms traditional paper-based systems into a fully digital backbone, allowing for immediate tracking of ingredients, production batches, and processes with both forward and backward traceability through digital tags that directly connect procedures to inventory. This modernization enables teams to manage recalls in just minutes instead of hours, integrating essential functions such as quality control, stock management, production oversight, documentation, and compliance into a cohesive environment. As a result, manufacturers gain real-time insights into their operations, which empowers teams to make quicker, data-informed decisions while ensuring they remain audit-ready through tailored reports and dashboards. The platform features an easy-to-use, no-code app studio, allowing users to recreate and customize their own workflows and standard operating procedures, centralize all documentation, automate scheduling and action management, and effectively handle instances of non-conformance. Additionally, by streamlining these processes, FoodOps enhances overall operational efficiency and reduces the likelihood of errors.

Trevally from ManualMaster is a comprehensive QHSE platform designed to cover the entire PDCA loop in a single web or on-premises solution. It provides controlled document and version management with audit trails, process mapping, risk and standard controls, as well as quality assurance registrations and smart web forms. Additional modules manage incidents, complaints, audits, deviations, tasks, and actions, all displayed in role-based dashboards with real-time KPIs, reports, and graphs. With ISO-27001 hosting, backups, single sign-on, two-factor authentication, and granular user permissions, Trevally ensures data security while supporting multi-language interfaces, digital signatures, and mobile access for enhanced user adoption.

ProCal is a robust calibration management solution created to modernize and standardize calibration operations. It replaces manual, paper-driven workflows with guided digital routines that improve accuracy and efficiency. Automated math, built-in tolerances, and real-time pass/fail indicators reduce errors and eliminate rework. The system centralizes calibration data, certificates, and audit trails in one secure, cloud-hosted platform. ProCal simplifies audits by automatically producing regulator-ready documentation with full traceability. Organizations can manage calibration schedules, reminders, and lifecycle tracking across multiple sites and teams. Compliance with ISO, GMP, FDA, and 21 CFR Part 11 requirements is enforced through secure controls and approvals. The platform supports enterprise scalability with configurable rules, user roles, and language options. Integration-ready tools connect ProCal with maintenance and asset management systems. The result is a reliable, efficient calibration program that grows with the business.

COOX is an advanced Manufacturing Execution System that transforms industrial operations by gathering, analyzing, and visualizing real-time production data. Acting as the operational heart of a smart factory, it connects directly with ERP systems and provides full oversight of manufacturing orders, equipment activity, resource usage, and material flow. Its model-based design allows COOX to adapt to any manual or automated production environment, making deployment quicker and more reliable across single plants or multi-site networks. Manufacturers rely on COOX for high-level functionalities such as performance analytics, OEE dashboards, quality monitoring, traceability, batch file generation, inventory management, and scheduling. The system delivers systematic process and product traceability to help industries comply with strict regulations and maintain high quality standards. From staff assignment to recipe and BOM management, COOX ensures every aspect of production runs smoothly and efficiently. Users from operations, quality, maintenance, and purchasing benefit from accurate insights and optimized workflows. With its modular MESbox suite and web-based architecture, COOX provides a scalable foundation for continuous improvement and Industry 4.0 transformation.

Food Guard is an app that helps small food manufacturers modernize and digitize their food traceability and compliance. We can trace ingredients, recipes and finished / complex products starting with the goods inwards step and continuing through the packaging, shipping, and cooking processes. Digitize all types of check sheets and also easy temperature monitoring - Audit with ease - Simple end to end traceability - Easy reporting 30% time savings compared to paper-based recording systems Get your free trial and Demo today. Call us now! Simple monthly subscription model, no contracts or large upfront investment needed !

Scada-Lite, the remote well monitoring system, consists of two separate parts: Well Manager and Field Data Capture iOS App. This IoT platform allows you to optimize your workforce, increase employee safety, and minimize nonproductive times. Scada-Lite Well Manager Well Manager provides real-time data about your field assets to help improve business performance. By making asset data available 24/7, Well Manager empowers you to: -Move from reactive to proactive maintenance -Prevent downtime and review production. -Increase staff productivity Scada-Lite Field Data Capture Application FDCA, a Scada-Lite product that is exclusively designed for mobile devices, allows field workers to capture information on field assets. It allows for electronic and other measurement and allows for timely decision-making.

CaliWare360 is a cloud-based Warehouse Management System (WMS) tailored specifically for the pharmaceutical sector, aimed at boosting operational efficiency. This system offers real-time inventory oversight, accurate material handling, and automated workflows designed to enhance warehouse performance. Key features encompass barcode and RFID integration, as well as FIFO and FEFO management, all of which aid in the organization and monitoring of inventory. Furthermore, the platform ensures adherence to Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP) by providing reliable traceability and comprehensive audit trails. It also integrates effortlessly with Electronic Batch Records (EBRs) and various manufacturing systems to streamline material handling. The presence of customizable dashboards and checklists fosters improved visibility and efficiency within warehouse operations. In addition, CaliWare360 is scalable, making it an excellent fit for businesses experiencing growth, while it simultaneously enhances retrieval efficiency and minimizes handling times, helping organizations thrive in a competitive market. With its innovative approach, CaliWare360 redefines how pharmaceutical warehouses manage their operations.

Luminata allows you to bring together all your process, chemical, and analytical data in one interface. This decision support software allows pharmaceutical development teams to collaborate without the need for spreadsheets or incompatible file formats. Applications include process control, forced degradation and batch genealogy, as well as characterizing composite materials.

Proconex Mobius Operations Software serves as a comprehensive industrial operations platform designed to eradicate manual, paper-based processes and eliminate information silos by seamlessly connecting personnel, systems, and workflows on the manufacturing floor, thereby offering real-time insights, digitization, and enhanced visibility. This platform empowers manufacturers to convert standard operating procedures, inspections, commissioning tasks, and routine checks into digital formats with guided mobile task execution, ensuring consistent data capture through methods like photographs, barcodes, and validation processes to bolster compliance and safety. Furthermore, it includes role-specific dashboards and analytics, which illuminate both current and historical performance patterns, highlight operational risks, and facilitate customizable reporting, enabling teams to identify irregularities, assess batch performance, and accelerate decision-making. Integrated alert systems monitor unusual activities with shift-aware notifications, and the platform also features modular applications such as ProofCheck, QuickView+, DataJaguar, and AlertTrack+, which can be utilized independently based on specific needs. Overall, Proconex Mobius provides a robust solution for modern manufacturing challenges, promoting efficiency and responsiveness across various operational facets.

EviView serves as a robust digital management system aimed at integrating and standardizing frontline operations within batch manufacturing sectors. By digitizing processes like shift transitions, tiered meetings, audits, and initiatives for continuous improvement, the platform connects teams to real-time data and key performance indicators, effectively replacing outdated Excel spreadsheets and paper logs. EviView is flexible enough to align with current processes and can grow as organizational needs change, while its single-tenant VPC hosting and SSO-over-SAML provide top-notch security for enterprises. Renowned companies in pharmaceuticals, biopharma, chemicals, food and beverage, energy, and various other batch industries rely on EviView to minimize downtime, enhance safety incident reporting, and foster ongoing improvement. The system not only offers browser-based dashboards and mobile accessibility but also converts disorganized data into meaningful insights, ensuring teams are unified under a single source of truth. This empowerment of managers to make informed, data-driven choices significantly enhances operational excellence and contributes to a culture of continuous improvement across the organization.

Landmark is a user-friendly platform that streamlines every aspect of the recording procedure while preserving the benefits offered by various systems. With Landmark, recorders can efficiently handle all official documents by electronically reviewing, approving, and indexing them, thus avoiding the hassle of managing physical files. The system features scan-first, batch scanning, and historical scanning workflows to enhance productivity. Once documents are scanned, the entire workflow is digitized, covering everything from indexing and verification to the issuance of certified copies. Users can easily apply electronic certifications directly on the screen for any certified document. Additionally, it allows for the attachment of electronic signatures, and the certification language can be tailored to meet the specific requirements of your County. Landmark eliminates the complications of juggling multiple databases and logins, granting recorders access to a unified database across the entire department and ensuring a consistent approach to information retrieval for all personnel. This comprehensive solution not only saves time but also improves accuracy and reduces the risk of errors in the recording process.

Biscom's Digital Transformation addresses the intricate challenges of fax and secure document delivery within the most strictly regulated sectors. Renowned for its reliability, Biscom serves prestigious organizations across healthcare, finance, and government. Their diverse offerings include Fax solutions tailored for On-Prem, Hybrid, and Cloud environments, ensuring secure, dependable, and scalable fax software and servers for mission-critical workflows compliant with HIPAA, FERPA, and SOX. Additionally, Biscom provides secure file transfer solutions, secure email and document delivery, and large file transfers, all adhering to HIPAA, SOX, and GDPR standards. For smaller enterprises, the Biscloud/SMB service delivers effective Fax Solutions and secure document delivery options specifically designed for regulated industries like healthcare—encompassing hospitals, laboratories, home healthcare providers, rehabilitation centers, and various pharmaceutical entities. Financial institutions, including investment firms, commercial, and retail banks, along with M&A consultants, also benefit from Biscom's innovative services. With Biscom, organizations can confidently navigate the complexities of secure communications and document management.

The impact of digitalization is profoundly reshaping our world, particularly within the industrial sector. The volume of data generated in contemporary industrial facilities is consistently on the rise, presenting new hurdles for SCADA solutions: vast quantities of information must be effectively managed and stored for extended periods. Simultaneously, there is a critical need to ensure that production processes are monitored and controlled to maximize reliability, efficiency, and productivity while continuously seeking optimization. With its adaptable and open system architecture for the seamless integration of data from the production level to MES/ERP systems and even cloud solutions, SIMATIC SCADA provides a robust answer to the challenges faced today and in the future. As digitalization unfolds, it opens doors to enhancing industrial processes, making them more flexible, customized, and efficient. Integrated approaches to production, encompassing everything from data gathering and analysis to informed decision-making, are essential components driving this transformation forward. This holistic view enables industries to not just keep pace with change, but to thrive in an increasingly complex environment.

PRIMS (Production Recipe Ingredient Management Software) offers an all-encompassing solution for food manufacturing, empowering users to manage their production workflows effectively. It manages every stage of the manufacturing process, from receipt of materials to the final shipping of products, granting users a holistic view of their operations. With the ability to track ingredients by Lot Numbers throughout the entire process—from receiving to production to shipping—users can maintain clear oversight of the contents of each batch and finished product. This tracking extends to sub-mixes, consumed ingredients, and packaging materials, ensuring complete transparency. Both intermediates and finished goods can have Lot Numbers that are auto-generated, streamlining the process. Additionally, compliance with GFSI traceability and recall requirements can be achieved in a matter of minutes instead of hours, enhancing operational efficiency. The software also allows for quick tracking of non-compliant ingredients, raw materials, and finished products, reducing time and waste. Furthermore, PRIMS simplifies the automation of both wet and dry ingredients, including flour, water, HFCS, oil, brew, and yeast draws, ensuring a more efficient production process overall. This level of detail and management not only improves accountability but also supports better decision-making in the food manufacturing industry.

Validfor is a robust and secure digital validation platform that consolidates the entire validation process into a single, paperless system, specifically tailored for industries that are heavily regulated. This platform not only streamlines validation tasks but also guarantees adherence to critical standards such as GAMP 5, 21 CFR Part 11, and EU Annex 11. With capabilities for handling electronic records and advanced electronic signatures, Validfor ensures complete audit trails, role-specific workflows (including Author, Reviewer, and Approver), and thorough CSV compliance. It securely organizes all documentation and records within a centralized repository, meticulously tracking every modification to maintain data integrity and uphold Quality Assurance. Additionally, Validfor provides integrated modules for Change Management, Deviations, Testing, and Periodic Reviews, thereby facilitating smooth impact assessments, tracking of CAPA, Computer Software Assurance (CSA), and management of audit-ready lifecycles. This comprehensive approach not only enhances operational efficiency but also strengthens compliance across various validation activities.

Alongside the need for consistent product quality and process reproducibility, batch processes face additional hurdles: Market and consumer expectations for product variety are on the rise, product life cycles are shortening, regulatory standards are expanding, and traceability control requirements, such as those mandated by the FDA, are tightening. To address all these batch automation needs and market challenges, the SIMATIC PCS 7 process control system provides an effective solution. The SIMATIC BATCH software suite, equipped with recipe support, adeptly handles even the most intricate tasks with adaptable control processes. Serving as the heart of batch operations, the SIMATIC BATCH Batch Control Center (BatchCC) facilitates the management, oversight, and regulation of batch processes, ensuring that manufacturers can respond to evolving demands swiftly. Consequently, utilizing such advanced systems enables businesses to maintain competitiveness and compliance in a rapidly changing industry landscape.