Alternatives to AmpleLogic Document Management

Compare AmpleLogic Document Management alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to AmpleLogic Document Management in 2026. Compare features, ratings, user reviews, pricing, and more from AmpleLogic Document Management competitors and alternatives in order to make an informed decision for your business.

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    Aizon

    Aizon

    Aizon

    Aizon: Intelligent GxP Manufacturing Aizon enables pharmaceutical and biotech manufacturers to transform operations with AI-powered solutions purpose-built for GxP environments. Our platform helps reduce variability, increase yield, and ensure product quality—consistently and at scale. Aizon Execute — Intelligent Batch Record (iBR): Digitize manufacturing in weeks, not months, reducing deviations and accelerating batch release. Aizon Unify — Contextualized Intelligent Lakehouse: Integrate and contextualize data across systems and sites to drive actionable insights for manufacturing excellence. Aizon Predict — GxP AI Industrialization: Deploy predictive AI to optimize critical process parameters, improve Right-First-Time rates, and boost yield. With Aizon, manufacturers move beyond compliance to achieve operational intelligence—analyzing the past, mastering the present, and shaping the future of production.
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    SimplerQMS

    SimplerQMS

    SimplerQMS

    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.
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    Adaptive Compliance Engine (ACE)
    ACE is a quality management software solution for companies of any size, in any stage, in any highly regulated industry. ACE is fully configurable allowing your company to adapt ACE to fit into your exact quality needs. Empower all levels of your organization with intuitive user interfaces, easily search for all your documents and records, and transform your data into actionable intelligence with advanced analytics all on a single platform. Our one-stop software includes: -Office 365 Integration -Inspection Management -Document Management -Risk Management -Product Lifecycle Management -Learning Management -Audit Management -Quality Events -Paperless Validation -Electronic Signatures (21 CFR Part 11 Compliant) -Endless Workflow Configurations -And so much more! ACE comes with everything you need, all included at one price. Every application is included, no more a la carte pricing. No more nickel and diming. One software, endless solutions.
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    MSB Docs

    MSB Docs

    MSB Docs

    MSB Docs simplifies digital document management for businesses of all sizes with secure, compliant, and legally binding Electronic Records and Electronic Signatures (ERES). It complies with US FDA 21 CFR Part 11, EU GMP Annex 11, and EU eIDAS (SES, AES, QES), making it ideal for regulated industries like healthcare and life sciences, while enabling cross-industry use across the EU. In India, MSB Docs adheres to the IT Act 2000 and supports DSC, Aadhaar-based eSignatures, and eStamping, making it the most trusted digital documentation platform. Trusted by leading organizations in pharma, BFSI, government, and education, MSB Docs offers: 1. eSign – Compliant digital signatures 2. CRA App – Simplified Clinical Research Associate workflows 3. Smart Forms – Dynamic, logic-based digital forms 4. eStamp – Legally valid, tamper-proof stamping MSB Docs enables organizations to digitize, manage, and automate document workflows.
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    AmpleLogic Learning Management System
    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.
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    AmpleLogic APQR
    Introducing AmpleLogic AI-based APQR software, a revolutionary solution that helps you generate accurate Product Quality Review (PQR) reports and CPV reports for audits and regulatory submissions as per the current Good Manufacturing Practices (CGMP) regulations for drug products (21 CFR 211.180(e), 21 CFR 211.180(e)). With OCR data extraction and AI chatbot integration, AmpleLogic APQR solution streamlines document data extraction and quickens access to information, boosting audit readiness and operational efficiency.
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    AmpleLogic Regulatory Information Management System
    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.
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    AmpleLogic eBMR
    AmpleLogic eBMR stands out with its modular design and low code platform, offering tailored solutions for pharmaceutical and biotechnology industries. With features like real-time integration, dispensing modules, and electronic signatures, it ensures compliance with global regulatory standards. AmpleLogic eBMR boosts productivity by automating quality checks, cutting compliance costs, and streamlining batch reviews. Its electronic records prevent errors, ensuring precise decision-making. The software speeds up product changes, meets regulatory standards, and improves efficiency in pharmaceutical manufacturing. Specify raw materials and weight-age calculations. Optimize material management with precise dispensing. Facilitates routing, reviewing, and approval of manufacturing records. Streamlined batch review process for increased productivity.
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    AmpleLogic Quality Management
    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.
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    Agatha

    Agatha

    Agatha

    Agatha offers a suite of cloud-based applications tailored to the life sciences industry, enabling centralized management of documents and processes across clinical operations, quality, regulatory, and training functions. It supports biotech, pharmaceutical, medical-device, and contract-research-organization workflows by offering modules such as eTMF (Inspection-Ready Master Trial File), Remote ISF (Investigator Site File) management, SOP creation and approval, Quality document management for CAPAs, deviations, and change controls, and regulatory document management. Agatha enables streamlined document creation, review, approval, storage, and sharing in one unified system, supports paperless transformation to reduce administrative burden and strengthen data security, and is built on a global-compliance architecture addressing standards like 21 CFR Part 11, GDPR, and EU Annex 11.
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    AmpleLogic LCNC Platform
    At Amplelogic, we are redefining the way life sciences companies navigate digital transformation. We offer a powerful suite of 14 SaaS products built on our advanced Application Platform as a Service (aPaaS), providing organizations with pre-configured, compliant solutions while offering the flexibility to build custom applications that seamlessly integrate with their existing systems. Our platform is designed to fill the gaps in your current solutions, enabling you to address specific challenges and accelerate operational efficiency. With Low Code/No Code (LCNC) capabilities, life sciences companies can easily tailor applications to meet their unique needs, without requiring deep technical expertise.
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    Slingshot Pharma

    Slingshot Pharma

    Slingshot Pharma

    Slingshot Pharma offers advanced pharmaceutical inventory management software designed for cGMP compliance. Our solution ensures real-time tracking, accuracy, and regulatory adherence for pharmaceutical manufacturing. Optimize inventory control, reduce waste, and enhance efficiency with our robust, scalable system. Stay audit-ready and streamline operations with Slingshot Pharma’s cutting-edge technology.
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    Ampleforth

    Ampleforth

    Ampleforth

    A new paper has been released. This report expands on the motivation, design, and performance of the Ampleforth protocol under live market conditions. AMPL is a cryptocurrency and financial building-block. Much like Bitcoin, it is algorithmic and uncollateralized. However unlike Bitcoin, AMPL can be used to denominate stable contracts. These supply adjustments are called "Rebases" and rebases occur once each day. When the AMPL network grows you'll automatically have more tokens, when the AMPL network shrinks you'll automatically have fewer tokens, but the price per AMPL will tend to cycle around $1. This novel rebasing mechanism is what allows AMPL to be used in contracts. AMPL is an independent financial primitive that does not rely on centralized collateral or lenders of last resort. It's like Bitcoin, except it can be used in contracts.
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    PleaseReview
    Ideagen PleaseReview is a document review, co-authoring and redaction software application that helps you to control and manage all aspects of the document creation and review process, delivering: Improved operational performance, productivity and efficiency, Stronger compliance and business oversight. Mitigation of regulatory, legal and commercial risk. PleaseReview is our document collaboration software, designed to make your collaborative process easier, safer and more efficient. Wherever you are working, and whether you’re collaborating with colleagues or third parties, PleaseReview provides a secure, controlled environment for real-time document review, co-authoring and redaction. So you can protect sensitive information and focus on delivering high-quality documents.
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    Veeva Vault QMS

    Veeva Vault QMS

    Veeva Industries

    Ensure quality and GxP compliance with Vault QMS. With built-in best practices and automated workflows, Vault QMS brings all parties – pharma and biotech companies, contract manufacturers, and suppliers – into quality processes for better control and visibility. Easily bring departments, sites, suppliers, contract manufacturers, contract test labs, and other partners into continuous quality improvement processes. Increase operational efficiency with automated workflows and built-in best practices. Improve risk visibility across products and processes with a unified approach to risk management. Improve speed, efficiency, and GxP compliance with a unified suite of quality applications. Readily enable quality management processes with built-in best practices for deviation, internal and external audits, complaints, lab investigations, change control, CAPA, and quality risk management.
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    AMPL

    AMPL

    AMPL

    AMPL is a powerful and intuitive modeling language designed to represent and solve complex optimization problems. It enables users to formulate mathematical models in a syntax that closely mirrors algebraic notation, facilitating a clear and concise representation of variables, objectives, and constraints. AMPL supports a wide range of problem types, including linear programming, nonlinear programming, mixed-integer programming, and more. One of its key strengths is the ability to separate models and data, allowing for flexibility and scalability in handling large-scale problems. The platform offers seamless integration with numerous solvers, both commercial and open-source, providing users with the flexibility to choose the most appropriate solver for their specific needs. AMPL is available across multiple operating systems, including Windows, macOS, and Linux, and offers various licensing options.
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    GoVal

    GoVal

    AdventSys Technologies

    GoVal is a paperless validation lifecycle platform for regulated industries like pharma and biotech. It supports IQ/OQ/PQ protocols, full document control, audit-ready trails, and compliance with FDA 21 CFR Part 11 and EU Annex 11. Role-based workflows and e-signatures streamline approvals. Dedicated risk assessment tools help evaluate change impacts and ensure regulatory alignment. Integration-ready via APIs, GoVal connects with ERP/LIMS systems securely. Real-time dashboards, alerts, and GoVal AI enhance efficiency by automating risk analysis, test case creation, and document drafting—unlocking intelligent automation with tangible impact. GoVal lowers manual validation overhead, speeds up audit preparation, and shortens product validation cycles—helping organizations realize ROI quickly.
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    docEdge DMS

    docEdge DMS

    Pericent

    Managing business information and documents from several sources becomes challenging, time-consuming, and dearer in cost. A fully-featured and power-packed document management system, developed and implemented by Pericent BPM & DMS Software Private Limited, can easily wipe out all the hustle that you face managing your business documents daily. docEdge DMS paperless document management system enables you to experience the effortless handling of all the business documents and information. We developed this program with several special features that allow it to stand among the topmost brands and most opted ones. Our expert team ensures easy and secure functionality of the program so that our end-user could derive ultimate satisfaction using it. docEdge DMS Basic is a complete Document Management System that provides great document management features. It is easy to use, powerful and cost-effective document management software.
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    Scispot

    Scispot

    Scispot

    Scispot powers life science labs with a unified LabOS™ platform, combining ELN, LIMS, SDMS, QMS, and AI in one configurable, no-code system. Built for CROs, Molecular Diagnostics, Pathology, Pharma QC, and Drug Discovery, Scispot streamlines sample management, inventory automation, and regulatory compliance. Connect with 200+ lab instruments and thousands of apps to eliminate data silos while maintaining FDA 21 CFR Part 11, GxP, GDPR, and HIPAA compliance. Scispot's AI tools transform experimental data into actionable insights, with flexible workflows that adapt as research evolves—without IT support. Trusted by 1000+ scientists globally, Scispot enables rapid deployment so teams focus on science, not administration. Accelerate discoveries, ensure compliance, and scale operations with a platform purpose-built for modern biotech innovation.
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    Ample Organics

    Ample Organics

    Ample Organics

    Ample Organics is a software company building technology to support cannabis businesses. Our work is helping to shape a world where access to safe cannabis is universal—it’s a once-in-a-lifetime opportunity. We’re developing tools that foster transparency, facilitate compliance, and build trust between cannabis licence holders, government bodies, and the public. Our clients use our products to create complete visibility into the origin and chain of custody of any cannabis product they produce. Ample Organics is a global leader in cannabis technology, providing innovative business solutions that facilitate compliance with government regulations. Our seed-to-sale platform operates in four countries and has been adopted by the majority of Canada’s licensed producers. Our clients rely on this platform to track and report every stage of business, from seed to sale, and from patient to government.
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    Scientist.com

    Scientist.com

    Scientist.com

    We built our marketplace to support the improved sourcing of regulated services. COMPLi® can provide an organizational structure for ensuring compliance, giving leaders peace of mind in the security of sourcing across multiple research areas. Automatically track purchases, manage contracts, handle payments, and upload spending data into your accounting system. Our award-winning platform helps pharmaceutical companies, biotechs, and academic labs source regulated services and materials from external third parties. Whether you're a researcher, a pharmaceutical procurement expert, or a service provider, COMPLi® can help you with your compliance and governance needs. COMPLi® also reduces the administrative burden on providers of regulated services, enabling efficient customer relationships that reduce costs and speed up scientific research. Improves compliance and governance within multiple regulated service areas.
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    Merit for Life Science

    Merit for Life Science

    Merit Solutions

    Cloud-first ERP is intentionally tailored for life science organizations. Merit for Life Science is cloud-first ERP purposely built for biotech, pharma, and medical device manufacturers. It advances Dynamics 365 finance and operations to connect your entire organization. Mapping resource qualifications to production requirements. Monitoring vendor relationships in procurement to help ensure quality standards are met in manufacturing. Providing your life science organization with visibility and transparency to deliver safe, innovative products and much more. Your organization has unique needs and we understand them. Get the full picture of what we offer. Delivering an industry-tailored solution that meets the rigorous requirements of pharma, biotech, and medical device companies. Improve your decision-making process with reliable, auditable accounting practices. Establish financial reporting standards for acquired entities or prepare for acquisition.
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    QbDVision

    QbDVision

    QbDVision

    QbDVision is a structured, cloud-based Digital CMC platform designed to accelerate drug development by transforming dispersed scientific data into actionable process intelligence. It enables pharmaceutical and biotech teams to capture, organize, and connect product and manufacturing knowledge across the entire development lifecycle, replacing siloed spreadsheets and document-centric workflows with a unified, data-centric framework. Its multidimensional architecture provides visibility into every input, variable, and objective within development processes, allowing users to evaluate how changes may impact downstream outcomes and overall product quality. By structuring data with standardized vocabularies and contextual relationships, the platform supports risk-based decision making, improves collaboration, and strengthens regulatory readiness.
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    Scilife

    Scilife

    Scilife

    Revolutionize your Life Sciences processes. Drastically improve the control, efficiency, and quality of your processes and products. Ensure inspection readiness at all times through our fully compliant platform, pre-validated according to GAMP5. Maintain total control over processes and documents, customize workflows to perfection, and automate where possible. Enjoy uninterrupted workflows and full traceability through seamlessly connected and integrated modules. Our dedicated team is ready to answer your questions at any time. Only a first-class Scilife experience will do! Our Scilife platform streamlines automates and organizes every process in your industry space, whether you’re in Medical Devices, Pharma & Biotech, or ATMP. Click below to discover which Scilife modules support your unique industry lifecycle stages. Our software is equipped with all the advanced quality tools you would expect, and a bunch more that go above and beyond!
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    RegDocs Connect
    RegDocs Connect gives your operational and regulatory teams the tools they need to prepare complete and compliant submission ready documents and records. Built with the end user in mind, collaboration, automation and quality are the foundation of this solution. Automated workflows manage your records lifecycle from draft to final, enabling your team to be in complete control of your regulatory documents at all times. Mapping of document types to the EDM reference model and eCTD facilitates organization and retrieval of documents for inclusion in regulatory submissions. Proprietary tools such as PDF/A Publishing, document classification, and unique document identifiers provide a powerful regulatory document management solution that pulls information from across your organization, into one manageable solution. With the rise of electronic submissions to regulatory agencies and the increased complexity of drug development, the ability to produce submission-ready, quality content
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    Doccept

    Doccept

    Kensium Solutions

    Doccept is a multi-user Document Management System (DMS) that allows businesses to securely organize content. A Document Management System (DMS) is essential for organizations that aspire to “Go Paperless". It can be overwhelming for today’s businesses to effectively manage the legacy of documents stored in different places. Electronic Document Management is a requirement for a variety of industries including Biotech & Pharmaceuticals, Media, Telecom, Manufacturing, Banking, and Tax/Accounting. When large amounts of client data or transaction histories need to be retained over long periods of time, Doccept can help. The concept comes with a detailed API guide, giving you the ability to integrate with any third-party application seamlessly. The concept supports integration with LDAP (Lightweight Directory Access Protocol) and Active Directory to map User authentication without creating a separate account.
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    CBO ERP

    CBO ERP

    CBO ERP

    CBO ERP Ltd is a leading provider of customized process-driven software solutions for the pharmaceutical industry. Their flagship offering is a 6-in-1 customizable pharma ERP system that enables pharmaceutical businesses to control and manage key aspects such as manufacturing, distribution, finance, web reporting, mobile and tablet access, and online HR payroll. This ERP system is designed to operate both online and offline, ensuring total control regardless of the situation. In the pharmaceutical industry, making a mistake is not an option. Customers rely on your products for their well-being and a mistake could be life-threatening. Due to the natural instability of the market, nearly every company is looking for a way to streamline their financial services and adopt improved financial models. Ecommerce means buying and selling goods, products, or services over the internet. Ecommerce is also known as electronic commerce or internet commerce.
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    M R Reporting Software

    M R Reporting Software

    E-Tech Services

    MRR is simple easy to use Pharma CRM software that does not require any specific knowledge of computers. Anyone and everyone who is conversant with general computer applications can easily (fill or file?) his ‘Daily Call Reports’ (DCR) and send the same that very instant to the company via the Internet, thus saving on the cost of courier services. Simultaneously, the Pharmaceutical crm software makes it possible for managers’ to assign task and delegate responsibilities to their team at any given point of time. The DCR thus filled – in by the sales representative in the field automatically gets updated in the company’s Management Database System and can be accessed by the company – both online and offline. All put together Pharmaceutical crm software saves lot of valuable resources in terms of TIME, MONEY and EFFORT, making the entire marketing process more dependable, fiscal efficient and transparent.
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    SOFTDMS

    SOFTDMS

    Pharma Soft Sol

    Pharmaceutical and Biotech companies are challenged to meet control documentation requirements in day-to-day operations. Effective document management and document control are critical parts to any quality and compliance solution. Global Regulatory agencies expect that all regulated companies follow current industry best practices throughout the manufacturing process. To meet these requirements Phama Soft Sol developed Document Management System software which helps to control and distribute the SOP’s , STP’s and other regulated documents. Document management software systems not only reduce the costs of compliance but also help you improve process and product quality. Document Management System(softDMS) able to retrieve the information you need exactly when you need it-minimizes the possibility of miscommunication and mistakes which in turn minimize risks, manhours and other documentation errors.
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    ysura

    ysura

    ysura

    ysura conceives and develops innovative Sales and Marketing Solutions for the Pharmaceutical Industry and offers them as a Software-as-a-Service. Founded in 2012 and based in Munich, ysura has together with the sister company MuniConS over 60 employees from 17 different countries. All of ysura’s shares are still held by the founders and the employees. With our state-of-the-art mobile Pharma-CRM Solution and MuniConS’ consulting expertise, we assist Pharma companies in their successful digital transformation. ysura is the old Celtic word for Isar, the river that flows through Munich. It comes from ys (fast) and ura (water). Ysura means fast water. A perfect description for our products: fast and perfectly adapted to the flow of tasks and information for the life sciences industry.
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    Cove Identity

    Cove Identity

    Cove Identity

    Share your sensitive data with anyone securely and easily, without compromising on privacy. Cove's advanced search feature makes finding documents a breeze - search by file name or smart tags to quickly locate the information you need. Transform paper to pixels, organize with ease, and maximize productivity while keeping your information protected. Safely share your files with others using Cove's secured links feature. With encrypted links and access control, you're always in control of who can access your data. Easily transfer large volumes of documents securely with Cove's bulk upload feature. Our end-to-end encryption keeps your data protected at all times. Get ample space to store all your important files securely with Cove's cloud storage.
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    Siguru AI

    Siguru AI

    Siguru AI

    Siguru AI is an AI-driven compliance and Medical, Legal & Regulatory (MLR) process optimization platform built for pharmaceutical and life-sciences teams to improve how commercial and medical content is reviewed, approved, and monitored across digital channels. It uses advanced artificial intelligence to accelerate MLR reviews, reduce errors, and flag compliance risks in marketing and digital materials, helping internal teams deliver review-ready, code-compliant content faster and cut down approval cycles by detecting issues before they escalate. It integrates into existing workflows and content management systems, supports automation of compliance checks in content creation, and provides real-time insights that align with global regulatory codes and standards, aimed at reducing complaints and oversights tied to digital promotional content.
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    B2

    B2

    CS

    B2 – single integrated solution, designed to meet the unique product needs of retail and commercial banks from front to back-office. The modular structure ensures broad coverage of financial and management field, as well as the flexibility to create and configure new financial products. In the basis of the structure there is the concept of continuous development and flexible capacity features. Fundamental part of the bank's business strategy is organizing the work with financial instruments and choosing the priority areas for contract relations with customers. B2ng provides ample opportunities for the development and implementation of new financial instruments. The versatility of the system covers functional needs for the generation the product line for any bank - small and large, universal and specialized on corporate or individual services.
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    Docs-IQ

    Docs-IQ

    Caliber Technologies

    Paper documentation means space, risk, and effort! Often, documentation is the source of 483s during FDA audits. An automated document control system helps enterprises overcome paper documentation issues. Docs-IQ is made for highly regulated industries as a web-based document management system. Switch to Docs-IQ system to align with company SOPS, GMP, and other regulatory guidelines. Pharmaceutical industries deal with diverse types of documents daily. In no time, the pharma companies will be drowned in paper documents if they maintain every little detail on the paper. Having a simplified system for document processes is the need of the hour. A document goes through 9 stages before it becomes obsolete or is destroyed. Management of the document lifecycle from the initiation stage to storage and finally destroyed in a manual paper-based company is difficult. At every stage of the document lifecycle, a lot of paperwork, time, effort, and resources get involved.
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    Evimple

    Evimple

    Evimple

    Evimple is an AI copilot for pharmaceutical business development that combines research, partner discovery, and market intelligence in one platform. It helps pharma companies evaluate opportunities, identify portfolio gaps, and find verified CDMO, CRO, and licensing partners in days instead of months. The platform aggregates medical, patent, regulatory, and commercial data and converts it into BD-ready insights, recommendations, and structured reports. It provides portfolio-driven partner matching, personalized monitoring of market signals (clinical trials, patent expiries, competitors, M&A), and access to verified warm contacts rather than scraped databases. Evimple supports the full BD workflow — from idea screening and deep evaluation to partner selection and deal preparation — reducing internal research cycles and accelerating decision-making. It is designed for SME pharma companies and BD consultants who need faster, data-driven expansion and partnership execution.
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    Quality Connect
    Enterprise Quality Management Software in the cloud for the life sciences. In today’s complex operational environment, technology plays a vital role in ensuring that QA is made aware of the issues as they happen. Gaining insight into the performance of your quality management system and the current state of your operation helps you to be more proactive, which minimizes risk and eliminates costly delays. Montrium has designed its Enterprise Quality Management system (EQMS) to enable life science companies to tackle the quality challenges that they face in content management head-on. All of our SharePoint QMS modules can be used independently or together as a fully integrated quality management system. These modules are available as part of our Montrium Connect Platform and can be deployed on-premise or in the cloud. Perfect for pharmaceutical companies, contract manufacturing organizations, medical device companies. Built to achieve compliance with GMP and GCP requirements.
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    Validfor

    Validfor

    Validfor

    Validfor is a secure, modular digital validation platform that centralizes the entire validation lifecycle on a single, paperless system. Designed specifically for regulated industries, Validfor enables efficient validation while ensuring full compliance with GAMP 5, 21 CFR Part 11, and EU Annex 11. The platform supports electronic records and advanced electronic signatures with full audit trails, role-based workflows (Author, Reviewer, Approver), and complete CSV compliance. All documents and records are securely managed in a centralized repository, capturing every change with full traceability to protect data integrity and Quality Assurance. Validfor offers integrated modules for Change Management, Deviations, Testing, and Periodic Reviews, enabling seamless impact assessments, CAPA tracking, Computer Software Assurance (CSA), and audit-ready lifecycle management.
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    Inova

    Inova

    Inova

    Inova accelerates life sciences partnering throughout the different steps of the lifecycle. Finding the right partner or opportunity is like finding a needle in a haystack. You have to sift through an endless number of clues to find the right information. Inova help you uncover promising new opportunities faster. From managing due diligence to negotiating final terms, the deal making process is long. Inova saves you time by simplifying and streamlining key processes. Once a deal is signed, the clock is ticking on making it successful and profitable. Inova helps you hit the ground running. Our market-leading digital partnering platform empowers over 160 pharma, biotech and life science organizations, to efficiently find, deal and collaborate. Cloud platform
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    iEnvision

    iEnvision

    Envision Pharma Group

    iEnvision is a comprehensive, web-based platform developed by Envision Pharma Group to enhance efficiency, compliance, and impact across the pharmaceutical product lifecycle. Purpose-built for medical affairs, it facilitates the strategic planning and management of evidence generation, grant programs, and communication activities. As a Software-as-a-Service (SaaS) solution, iEnvision supports rapid deployment and enterprise-level scalability without requiring IT department installation or packaging. The platform offers a unified user interface accessible via a single URL, with each solution preconfigured with baseline workflows that align with industry best practices. Integration is streamlined through iEnvision's APIs, supporting features such as Single Sign-On (SSO), eSignature, and citation retrieval, while also providing multiple language support.
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    PharMethod

    PharMethod

    PharMethod

    PharMethod is a leading partner for speaker bureau management solutions, meetings, and events management, and dynamic online customer engagement platforms. Their comprehensive 360° solution for pharmaceutical speaker bureau management includes the state-of-the-art online portal PharmaSpeak, meeting services, KOL and speaker management, strategic account management, aggregate spend data and reporting, and compliance monitoring and oversight. PharMethod's meeting and event management services encompass full-service program design and delivery with local, national, and global reach, offering live, virtual, and hybrid event management, event planning and design, meeting management services, production, staging, and audio-visual support, attendee engagement and content delivery, and financial and critical data management. Their HCP engagement platforms provide powerful, personal, virtual HCP engagements through media resource centers offering on-demand content for HCPs.
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    Logical Access
    LOGICAL ACCESS® SUITE is a document management and archiving software. LOGICAL ACCESS® SUITE, particularly solid and secure, is a very modular/flexible solution and can be customized according to the clients’ needs. LOGICAL ACCESS® SUITE allows the management and filing of all Spools/Cold documents, digitalisation of all paper documents (with automatic filing of documents with barcodes recognition or OCR) and the filing of all Office documents, Mail or PDF. Due to a strong historical establishment in the banking environment, LOGICAL ACCESS® SUITE ensures a reinforced security of the information archived: documents can be electronically signed (to guarantee their non-modification from the moment they are filed), encrypted (in order to guarantee their viewing is made only within the protected framework of the application) and even compressed. Secured solution for filing and document management.
    Starting Price: $100000.00/one-time
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    SmartReps
    SmartReps enables field sales reps to effectively manage their interaction with healthcare professionals while optimizing sales performance. The whole CRM pharma is dedicated to the life sciences Industry and was built to enhance field reps' effectiveness. SmartReps perfectly match the operational needs of medical sales representatives and adapt perfectly well to your commercial activity. Whether online or offline, reps can leverage CRM pharma and historical visit data to prepare calls and personalize each HCP interaction. It’s time to give your medical, hospital, or pharmaceutical representatives, the means to succeed! Smartreps give field reps all tools they need to interact with HCPs through different channels for a seamless and personalized omnichannel experience. Whether face-to-face or virtually, reps can always deliver the most relevant message to HCPs. With Smartreps, field reps can collect and capture any relevant information from HCP.
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    K2C eSignature for SharePoint
    K2C eSignature enables the use of SharePoint (from 2010 up to 2019 version) to electronically sign any document or record in compliance with US 21 CFR part 11, European Annex 11 and similar regulations. After the installation, a new action "eSignature" is available both in SharePoint Designer or Nintex workflow, if you are using this additional tool. This action can be added at any step of the workflow, in order to collect one or more user signatures without the need of any custom development or coding knowledge. Including views to verify eSignature records for selected item/document and reports dedicated to managers in order to display all electronically signed items/documents in a given SharePoint site and in selected year/month. Able to dynanically retrieve the appropriate signer from any SharePoint list that is managing the assignement of company roles.
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    K2C PSMF Solution
    K2C PSMF Solution is a modern approach to the management of the Pharmacovigilance System Master File. This document typically requires periodic updates as per significant changes in the pharmacovigilance process. These changes require that multiple company roles are involved in editing a document that is composed of paragraphs and annexes that are all the time same because fixed by regulations. However co-editing is complex; in addition, part of the content should be reserved to some editors and even not available to other contributors. K2C solution allows handling the distinct paragraphs and annexes as single documents, then it offers the possibility to create the PSMF document as a merge of various source documents. K2C PSMF Solution includes management of PSMF contributions (paragraphs and annexes) as distinct documents; management of access rights for viewing or editing of PSMF contributions; and management of the entire lifecycle.
    Starting Price: €8,500 one-time payment
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    RxERP

    RxERP

    RxERP

    RxERP is a cloud-hosted, industry-specific enterprise resource planning software built exclusively for the pharmaceutical supply chain with serialization embedded at its core, allowing unit-level tracking from manufacturing through distribution to help meet complex regulatory requirements such as the Drug Supply Chain Security Act. It integrates compliance automation, traceability, and anti-counterfeiting tools into daily operations, streamlines audit procedures and reporting, and enhances transparency throughout the supply chain. It provides business intelligence analytics from a centralized data software so users can make informed decisions based on real-time insights, and supports financial automation for improved cash flow management and reduced risk of bad debt. RxERP also offers inventory management to optimize stock levels and boost order fulfillment, CRM functionality to personalize interactions & strengthen customer loyalty.
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    Cardstream

    Cardstream

    Cardstream

    Cardstream provides white-label payment gateway solutions for software companies, acquirers, payment services providers, independent sales organizations and other value-added service providers. The powerful open payment network manages the whole payment process across different countries. Cardstream is a high-performance Level 1 PCI: DSS-compliant white-label payment processing platform, adding value by offering all major credit card schemes and worldwide currencies. At Cardstream, we offer ample partnership opportunities from co-branding to a full white-label payment gateway.
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    MetaTrader 4

    MetaTrader 4

    MetaQuotes

    MetaTrader 4 is a platform for trading forex, analyzing financial markets and using expert advisors. Mobile trading, trading signals and the market are the integral parts of MetaTrader 4 that enhance your forex trading experience. Millions of traders with a wide range of needs choose MetaTrader 4 to trade in the market. The platform offers ample of opportunities to traders of all skill levels: advanced technical analysis, flexible trading system, algorithmic trading and expert advisors, as well as mobile trading applications. Signals and market additional services extend MetaTrader 4 frontiers. The signals service allows you to copy trades of other traders, while the market provides you with various expert advisors and technical indicators that you can buy.
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    Pharmalite

    Pharmalite

    Pharmalite

    Pharmalite streamlines your commercial operations with smarter account management so your field team can generate more meaningful interactions. Pharmaceutical companies have made sizable investments in sales force effectiveness (SFE). Companies need to provide their reps with valuable tools to maintain sales effectiveness in order to reach the right professionals with the targeted product. While companies have upsized and downsized, maintaining the right number of reps is crucial. Training, coaching, pharma tools, and enablers provide efficiencies. Streamlining these tasks will cut costs without cutting knowledge. Give your field team the tools they need to generate more meaningful interactions with their HCOs and HCPS. Pharmalite streamlines Interaction creation with group interactions, auto-create from virtual meetings, and creates from a calendar. Automated mobile alerts let your team know when it's time to follow up.
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    Point of Success

    Point of Success

    Inborne Technology

    Point of Success is known for its low price and ample feature list. Not only is the software inexpensive, but other aspects of doing business with us are also very attractive. Point of Success software can help any restaurant or bar run more efficiently. No matter whether you run a coffee shop, table service restaurant, doughnut shop, deli, pizzeria, or any other type of restaurant or bar, Point of Success will make your operation more efficient while saving money!
    Starting Price: $299 one-time payment
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    PharmaCODE

    PharmaCODE

    SoftDent

    Powerful data search tools allows quick access of the data. An innovative and easy-to-use calendar is a great help for medical representatives in arranging their appointments. Various report generation and data analysis tools provide the possibility to dissect different sections of representatives’ work. Additional time dimension allows analyzing changes in dynamics of customer characteristics as well as a target setting for different time periods. Online. The application connects to central database directly. Offline. User can use the application offline without any limitations and synchronize the data when the internet connection is available. PharmaCODE is the newest customer relationship management (CRM) solution provided by SoftDent for pharmaceutical representative companies. This application was created combining newest technologies and all the experience that we have gathered during nine years developing, supporting and maintaining Customer Profiling.