Alternatives to Siguru AI

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

  • 1
    Veeva Vault PromoMats
    Built-in digital asset management for life sciences enables global reuse and reduces spend on promotional materials. Marketing teams can easily publish and withdraw content to digital channels and ensure only approved assets are in use. Accelerate content approval and time to market with industry-leading medical, legal, and regulatory (MLR). Built-in claims library with reference links reduces the administrative burden and risk of managing claims across countries, channels, and assets. Our industry cloud solutions provide data, software, services and an extensive ecosystem of partners to support your most critical functions from R&D through commercial. Veeva helps companies of all sizes bring products to market faster and more efficiently and maintain compliance.
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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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    Pepper Folio
    With Pepper Folio, commercial and medical teams get easy, tailored access to on-brand, approved content. Empower sales reps and medical science liaisons (MSLs) to seamlessly view and retrieve the appropriate content they need to engage key stakeholders. Once the content is approved in Pepper Flow, you can automatically push it to Pepper Folio so your teams can easily access on-brand content for both global and local markets. Pepper Folio’s features ensure that your content’s journey from review to approval to dissemination is fully automated. As content is approved for use, modified, or expired in Pepper Flow, it is automatically updated or removed from Pepper Folio to ensure compliant content usage. As a result, your team has one central repository for the latest and greatest content to support effective and engaging meetings. The marketing and operations team can access content usage analytics to identify which pieces of content are resonating the most with your key audiences.
  • 4
    Pepper Flow
    Pepper Flow’s unique features are built specifically to help life science companies streamline how marketing, medical, legal, and regulatory professionals work together. As a marketer, you need tools that allow you to move fast and keep things simple during advertising and promotional reviews. Get your critical campaigns and content to market to support your organization’s strategic initiatives. Maximize productivity by collaborating in real time to address feedback and turn around revisions. Spend less time managing the review process and more time on your high-priority to-dos. Pepper Flow is cloud-based, enterprise-grade software that enables life science companies to improve their competitive advantage, market products with efficiency, and maintain rigorous compliance. You need to move fast in order to deliver content to your key audiences. Pepper Flow’s intuitive interface allows you to get work done quickly and effectively.
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    Noah AI

    Noah AI

    Noah AI

    Noah AI is an AI-powered research assistant tailored specifically for life-sciences professionals, designed to automate and accelerate complex workflows across biomedical research, clinical development, and commercial strategy. It offers an “Agent” mode that plans and executes multi-step tasks by conducting intelligent web searches, querying trusted scientific databases (such as PubMed and FDA/NIH sources), summarizing high-impact papers, mining clinical-trial results, and generating professional-grade reports, while a lighter “Search” mode allows rapid, reliable access to domain-specific content summaries. With integrations across comprehensive medical/public-health data, AI-driven insights, and real-time news tracking of global R&D activity and conference intelligence, Noah AI enables researchers, biotech investors, and clinicians to go from question to insight in a fraction of the time.
    Starting Price: $12.40 per month
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    Veeva Vault

    Veeva Vault

    Veeva Systems

    Bridging content gaps across the enterprise for global harmonization, while supporting local autonomy. Veeva Vault is a true cloud enterprise content management platform and suite of applications specifically built for life sciences. Traditionally, companies have had to deploy applications for content and separate applications to manage associated data. Veeva Vault is the only content management platform with the unique capability to manage both content and data. Companies can now eliminate system, site, and country silos and streamline end-to-end processes across commercial, medical, clinical, regulatory, quality, and safety. Because all Vault applications are built on the same core platform, companies gain additional efficiency and compliance through the streamlined flow of documents across regions and departments. Content stays accessible, current, and in context across the entire development and commercial lifecycle.
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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.
  • 8
    MODA

    MODA

    Lonza

    The MODA Platform is a comprehensive solution designed to combine manufacturing and laboratory data into a single unified source to accelerate pharmaceutical product release and eliminate manual, error-prone workflows. The platform is user-centric, modular, and scalable, allowing organizations to start with the module that matches their current needs and expand over time. The three main modules are MODA-EM for Quality Control, automating the full spectrum of QC activities; MODA-ES for Manufacturing, enabling intuitive, flexible electronic batch records; and MODA eLogs for electronic logs, providing user-friendly, compliance-enforcing digital logbooks. The platform was developed specifically for the pharmaceutical industry to support digitalization of operations and address issues tied to paper records, such as prolonged cycle times for approval and review, missing or incorrect entries, and calculations that introduce risk.
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    Haast

    Haast

    Haast

    Haast is an AI-powered marketing and content compliance platform designed to help enterprises automatically detect and resolve brand and regulatory risks across their digital presence. It replaces slow, manual legal reviews by enabling marketers to self-check content while giving legal teams faster, more reliable oversight aligned with company policies and risk tolerance. Using advanced machine learning and large language models, Haast analyzes text, images, PDFs, videos, and web content to flag real compliance risks and provide actionable fixes before materials go live. It supports both pre-publication review and continuous live monitoring, scanning websites, social channels, and partner content to identify issues that could lead to reputational damage or regulatory fines. Its AI adapts to each organization’s internal rules and evolving regulatory environment, ensuring consistent standards across teams and geographies while reducing false positives.
  • 10
    CodeComply

    CodeComply

    CodeComply

    CodeComply is an AI-powered plan review and compliance platform built to automate, streamline, and improve the accuracy of building plan reviews and code compliance checks for the architecture, engineering, construction, and facility management industries. It lets users upload building plans in minutes and receive instant AI-driven compliance analysis that flags issues before submission, reducing costly errors and rework, and helping projects advance faster toward approval. It includes features like automated code compliance checks against IBC, NFPA, ADA, FHA, and local amendments, Readiness reports to catch missing elements, VersionVue automated version comparison, smart issue tracking and commenting, real-time collaboration tools, and structured compliance reports with visual insights for easy interpretation and sharing.
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    LighthouseAI

    LighthouseAI

    LighthouseAI

    Amid escalating pharmaceutical supply chain regulations, manufacturers, distributors, and 3PLs face mounting costs and non-compliance risks threatening revenue. LighthouseAI™ leverages compliance automation to solve compliance challenges, while reducing your stress and workload. Compliance is achieved in minutes, not days, resulting in the protection of your revenue stream from any adverse actions. Generate immediate compliance assessments for your facilities and erase hours of manual research to focus on actionable items. Receive instant regulatory updates and notifications regarding new and changing requirements and legislation relevant to your facilities. Organize your data on a single platform to achieve transparency with a bird’s eye view of your compliance activities.
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    Cloudbyz Safety and Pharmacovigilance (PV)
    Cloudbyz Safety & Pharmacovigilance Solution is a cloud-based software solution designed to streamline the drug safety and pharmacovigilance operations for pharmaceutical and life science companies. The solution helps to automate the process of collecting, processing, analyzing and reporting adverse event data in compliance with global regulatory requirements. Cloudbyz Safety & Pharmacovigilance Solution enables companies to reduce risk, improve compliance, and enhance patient safety while accelerating drug development. Cloudbyz provides end-to-end management of the pharmacovigilance lifecycle, including adverse event processing, case management, regulatory reporting, signal detection, and risk management. With Cloudbyz, you can optimize your pharmacovigilance processes, accelerate case processing, and increase the accuracy of your safety data, while minimizing risk and ensuring compliance.
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    Logwise

    Logwise

    Logwise

    Logwise is a compliance management tool that simplifies and automates regulatory workflows, helping organizations streamline key compliance processes like insider list management, market soundings, personal account dealing, restricted lists, conflict of interest tracking, PDMR obligations and policy management in line with UK and EU financial market regulations. It combines legal expertise with smart technology to reduce manual work and oversight risk by providing structured workflows, automated reminders, full audit trails, role-based access control and customizable modules that adapt to regulatory changes. Logwise centralizes documentation and compliance records, ensuring they are complete, easily accessible and review-ready for both internal teams and regulators. Designed for teams of all sizes, it supports cross-functional collaboration with secure, automated tools and helps organisations maintain transparent, and auditable processes across departments and stakeholders.
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    AmpleLogic Document Management
    AmpleLogic EDMS Software is a power-packed electronic document management system exclusively designed for Pharmaceutical and Biotech companies, developed, and implemented exclusively to meet the cGMP needs of Pharma domain with 21CFR Part 11 compliance, EU Annex 11 compliance can easily eliminate all the challenges faced by different companies AmpleLogic EDMS is a paperless document management system enables you to experience the effortless handling of all the documents and information. Various activities like document creation, review, approval, editing, document comparison, version control, parallel reviews are part of AmpleLogic Document Management System.
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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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    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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    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.
    Starting Price: $2000
  • 18
    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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    CaliberPulse

    CaliberPulse

    Caliber Technologies

    CaliberPulse is a specialized statistical analysis platform tailored for the pharmaceutical industry, designed to turn complex data into actionable insights for improving process efficiencies and compliance in quality control and manufacturing operations. It offers integrated reporting features that provide instant insights into statistical process control and statistical quality control data, with a focus on pharmaceutical needs. The platform integrates seamlessly with MS Excel, LIMS, EBR, and SAP, enabling efficient data extraction and real-time reporting with minimal manual effort. It includes advanced features such as automatic Box-Cox data transformation, critical attribute analysis, and data visualization tools, providing easy-to-understand results with graphical outputs and color-coded views. The system ensures compliance with regulatory standards by automating data ingestion and storage with full traceability.
  • 20
    Karomi

    Karomi

    Karomi Technology

    Karomi offers a cloud-based packaging and artwork lifecycle management system for Pharmaceuticals and Consumer Packaged Goods(CPG) companies. Our platform introduces efficiencies in every step of your artwork's journey - starting from collating content, designing the artwork, having it reviewed and approved by your internal and external stakeholders, and finally releasing it to your markets. As a result, it helps organizations in regulated industries reduce reworks and approval times, achieve compliance, and significantly reduce their product’s time-to-market. The system can be used by all internal department users like Regulatory, Packaging, QA, Marketing, R&D, Medical Affairs, Legal, etc. and by external stakeholders like print vendors, artwork studios, LLPs, 3rd party, CMO and CPO. Graphics, Text, Barcodes, and Braille can all be inspected and compared across artworks. The measurement tool allows accurate measurement of lengths & areas and the annotation tools.
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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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    Qualis LIMS

    Qualis LIMS

    Agaram Technologies

    Qualis LIMS is an enterprise-class laboratory information management system used in industrial, analytical, & commercial sample testing across several industry verticals such as pharmaceutical, life-sciences, contract research, clinical research etc. Qualis LIMS has built-in integrated modules to manage all laboratory processes & help labs perform their tasks in an automated and paperless manner while enabling them to fulfil regulatory compliance requirements & adhere to industry standards. It digitally transforms labs by helping them: • In managing, storing, & aliquoting of samples. • Record final results of tests & experiments - manage tests, projects, samples, instruments & inventory in one central secure database. • Meet data integrity & regulatory compliance requirements such as GxP, ISO17025, 21 CFR Part 11 & EudraLex Annex 11 without any compromises.
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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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    SANeForce

    SANeForce

    SANeForce

    SANeForce is a comprehensive customer relationship management (CRM) and sales force automation (SFA) solution tailored primarily for pharmaceutical, healthcare, and life sciences industries. Designed to enhance the productivity of sales and marketing teams, SANeForce offers features like real-time order management, expense tracking, inventory control, and territory management. The platform also supports medical representative (MR) reporting, enabling field sales personnel to log visits, capture doctor interactions, and manage appointments directly from their mobile devices. With data-driven insights and analytics, SANeForce helps organizations track performance, streamline processes, and optimize customer engagement strategies. Additionally, the solution includes features for compliance management, making it a reliable choice for highly regulated sectors that require meticulous record-keeping and adherence to industry standards. Visit: www(dot)saneforce(dot)com
    Starting Price: $10/user/month
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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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    SmartContent
    SmartContent enables marketing teams to effectively engage with healthcare professionals, through a seamless and personalized experience. You don’t need any more certified digital agencies to create your own content! Take back control of your marketing tools and expenses. With SmartContent, marketing teams can easily manage all marketing materials such as visual aids, dedicated microsites, or polls. Make available to your reps the right content automatically according to the profile of each HCP, while ensuring compliance rules for your content. Marketing teams can capture instant insights from call sessions, allowing you to refine and improve for greater market success. Interact with healthcare professionals through different digital channels, for a seamless and personalized omnichannel experience. In just a few minutes, create your marketing templates without the need to code, segment your database, create workflows to get the best impact, and analyze campaign KPIs.
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    ZAIDYN
    ZAIDYN is an AI-powered, cloud-native platform developed by ZS to revolutionize the life sciences industry. It integrates advanced analytics, machine learning algorithms, and intelligent workflows to empower organizations in transforming processes across research and development, commercialization, and patient engagement. The platform's modular design allows for scalable solutions tailored to specific needs, facilitating seamless integration with existing IT infrastructures through its open architecture. ZAIDYN enhances cross-functional collaboration by providing unified, high-quality data and insights, thereby reducing operational silos and promoting informed decision-making. With a focus on security and compliance, the platform ensures data privacy and adheres to regulatory standards, making it a reliable choice for life sciences companies aiming to innovate and improve health outcomes.
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    BookVision CLM
    BookVision CLM has been designed for a better field engagement with the doctors. Present your content to doctors. Understand what information they need and require. Showcase important things and more. With BookVision CLM you integrate e-Detailing, remote detailing, e-mail interaction, doctor portal and much more. Such universe is called “Project Multichannel” The Media-Soft creative studio department enables us to design the content for your CLM tool. If you want 3D Modelling, comprehensive videos, charts and flashy animations we can design them all. But sometimes pharmaceuticals want to be in charge of content design, and that is why we created the Booki component, within which you can easily add/change/edit your own content. Upload pdf, pots and other formats, and Booki will transfer them to HTML5 and deploy them to medical rep devices.
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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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    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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    Platforce CRM

    Platforce CRM

    Platforce

    Platforce CRM is a cloud-based all-in-one Closed-Loop Marketing, Customer Relationship Management and eDetailing solution for pharmaceutical and life science companies to automate industry-specific business processes and improve customer engagement. The System allows you to provide the marketing and sales activities in full: from the marketing cycle initiation through databases creation, territories assigning, and calls carrying – to KPI analysis. The platform includes a handy built-in planner to schedule medical representative activities; and its parameters are configurable enough to meet your business requirements. Among other functions, the Platforce CRM allows various calls performance, including remote calls, and statistics analysis after the call.
    Starting Price: $15/month/user
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    Symmetryk

    Symmetryk

    Symmetryk

    Symmetryk is an engagement software platform built from the ground up for the life-sciences industry, simplifying the way field teams connect and engage with the healthcare community. It enables easy access to scientific content, ensuring field teams have the right resources at their fingertips during interactions. By streamlining content discovery, customization, and compliance, Symmetryk equips customer-facing teams with the tools to deliver impactful presentations, engage in meaningful discussions, and build strong relationships with healthcare professionals. The platform allows access to content anywhere, whether in a physician's office, a hospital basement, or on a flight, ensuring content is always up-to-date. Symmetryk is built with a highly streamlined content database, enabling access to any piece of content in just three clicks. It provides granular analytics on content utilization and insights into which content is appreciated by medical science liaisons.
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    Salesforce Agentforce Life Sciences
    Agentforce Life Sciences, formerly Life Sciences Cloud, is Salesforce’s AI-first engagement platform built for Pharma, MedTech, Consumer Health, and Animal Health organizations. It unifies clinical, medical, commercial, and patient services functions on a compliant, industry-specific CRM foundation. The platform enables cross-functional teams to engage healthcare providers and patients using real-time, data-driven insights. AI-powered automation accelerates clinical trials, improves medical inquiry management, and enhances commercial engagement. Life Sciences Cloud supports compliant workflows with audit trails and governance embedded directly into daily operations. Patient services teams can streamline benefits verification, adherence programs, and adverse event management. Agentforce Life Sciences helps organizations bring therapies and devices to market faster while improving operational efficiency and stakeholder engagement.
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    Amici

    Amici

    Amici Procurement Solutions

    MyAmici is a cloud-based LabOps platform that integrates purchasing, supply-chain, inventory, and procurement software for biotech and life-science labs into a single, unified system. It connects the lab’s internal systems (e.g., ERP, inventory databases, supplier catalogs, order & invoicing tools) with external suppliers and vendors so that information flows in real time, enabling labs to maintain a consistent, reliable “single source of truth” for procurement, stock levels, consumption, invoices, and delivery statuses. This integration ensures that product catalog changes, order placements, deliveries, and invoicing are synchronized automatically between supplier systems and the lab’s internal records, eliminating manual data entry and reducing the risk of errors. MyAmici supports end-to-end lab procurement workflows, from requisition, purchase order, order tracking, receipt, inventory logging, asset, and consumables management.
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    Citeline

    Citeline

    Citeline

    Citeline is a clinical development intelligence and analytics platform that provides real-time R&D data, insights, and tools to life sciences organizations to inform strategic decisions across the drug and device development life cycle. It aggregates and curates the world’s most extensive datasets on global clinical trials, investigators, trial sites, drug development pipelines, and regulatory requirements, supporting functions such as protocol design, feasibility analysis, site and investigator selection, enrollment forecasting, competitive benchmarking, and compliance tracking with disclosure obligations across jurisdictions. It includes products like Pharmaprojects for pipeline monitoring, Trialtrove for clinical trial benchmarking, Sitetrove for site/investigator intelligence, Global Patient Insights for aligning feasibility with real patient access, and TrialScope Intelligence/Disclose for managing regulatory disclosure requirements.
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    Lylli LaunchTools

    Lylli LaunchTools

    Lylli LaunchTools

    Pharmaceutical & Medical Device companies lose $1 million to $13 million dollars a day for every day of delayed launch. Avoid costly mistakes with Lylli LaunchTools which helps you launch Better, Faster & Smoother. Doing this gets the products into the hands of patients faster, improving and saving lives! This keeps your stakeholders happy, facilitates your bonus and makes you look like a Hero to your boss. Ideal for Global, Regional or Local Product Launch teams of 10 or more, In Pharmaceutical, Medical Device companies & Agency partners who support them. Lylli LaunchTools displays Visual Go go-to-market strategy roadmap - dynamic & interactive in a 2-D environment. This helps Pharmaceutical & Medical Device companies Launch Better, Faster & Smoother. Lylli LaunchTools helps you manage several product launch processes from a single workspace, with ease. This is a very easy to use software Start for Free Today. No Credit Card Needed.
    Starting Price: $99.90 per month
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    SAP Advanced Track and Trace for Pharmaceuticals
    Protect your business and meet country-specific requirements for drug serialization and other fast-changing regulations while handling large volumes of data with intelligence. Comply with international and regional legislation using the SAP Advanced Track and Trace for Pharmaceuticals application, which provides a corporate serialization repository, serial number management, and regulatory reporting capabilities. Reduce compliance costs for existing and upcoming serialization requirements, such as country-specific reporting. Boost the efficiency of your supply chain with greater visibility into material movements, down to the sales-unit-item level. Handle large volumes of serialization data and adapt to new legislation. Track and trace the serial numbers of retail products in a corporate repository. Comply with country-specific regulations when reporting serial numbers.
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    SmartTeam
    SmartTeam enables sales & operation managers to monitor and enhance teams' performance. Implement data-driven strategies and transform your data into actionable insights! We have built the whole software suite with life sciences managers. Manage your sales and distribution channels effectively, enhancing sales teams’ performance and improving business results significantly. SmartTeam allows managers to monitor business conditions, products, and deliveries from a flexible and complete administration interface. SmartTeam provides access to your sales and operation managers to real-time information from the field. Benefit from a powerful Business Intelligence tool that allows you to track all relevant KPIs for your commercial performance. Using Euris solutions, sales, and operation managers can quickly create, update, share, and analyze e-learning content. E-learning can be synced to product launches and can be used to train medical representatives to meet the needs of the market.
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    Puntt AI

    Puntt AI

    Puntt AI

    Puntt AI is a review automation platform built for regulated enterprise brands that automatically checks marketing and packaging assets for brand, regulatory, and legal compliance inside the tools teams already use. It replaces slow manual review processes by using AI agents to analyze creative materials, identify risks, and recommend fixes, helping organizations compress approval cycles from weeks to hours. It integrates directly with common project and design systems such as Wrike, Asana, Figma, Adobe Creative Cloud, Google Drive, Microsoft 365, Jira, and Esko, allowing teams to run compliance checks without changing their existing workflows. It can automatically flag issues such as prohibited claims, incorrect packaging elements, or spelling errors, enabling faster iteration and reducing costly rework.
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    Syneos Health

    Syneos Health

    Syneos Health

    Syneos Health offers comprehensive medical affairs capabilities to help pharmaceutical and biotechnology companies navigate the complex medical and scientific landscape. Their services encompass medical strategy development, field medical deployment, real-world late-phase studies, health economics and outcomes research, and scientific communications. By acting as an extension of your team, Syneos Health aims to amplify your scientific narrative and value proposition to a diverse range of stakeholders, enhancing patient care and optimizing product launches. Their integrated approach ensures the effective demonstration and communication of your product's safety, efficacy, and impact on patient outcomes.
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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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    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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    HSO Life Sciences
    The life sciences industry is one of the most complex in the world. These companies need a responsive IT infrastructure with the ability to control compliance costs. Improving business performance as you work to bring new products to market in a timely manner is critical. The explosion in the need for research, development, and regulatory compliance is driving the demand for a more flexible operating environment. Nothing is more critical than access to real-time information on production processes and business operations. Life science companies depend on this data to make sound business decisions, maintain compliance, and run efficiently. Time-to-market and profitability pressures are intense. Many times, being the first company to market and patent a new product is a key indicator of potential success. Often these needs are balanced against demand for manufacturing existing products.
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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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    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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    Lyriko

    Lyriko

    Hyntelo

    Lyriko is a platform that boosts commercial efficiency and content effectiveness by leveraging AI & automation. It allows your business to effectively manage your customer base by providing actionable insights for sales reps and content journey orchestration. Lyriko helps Life Science organizations achieve the Next Best Action paradigm of omnichannel engagement. Being a scalable and modular platform, Lyriko is a full-fledged AI solution that covers all your needs in the realm of commercial operations, at a global level.
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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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    policyIQ

    policyIQ

    policyIQ

    Take the stress out of SOX compliance with policyIQ, by simplifying oversight and maximizing efficiency. With the easy configuration tools in policyIQ, our solution will meet your unique needs and will be ready to go within weeks – without the heavy price tag of a custom solution. Save time and reduce error by updating a control just once, with changes flowing through all reports and views. Gain oversight with customized dashboards to see progress and results in real-time. Be proactive in the collection of audit evidence by issuing requests for documentation in advance. Automate control attestations, reviews, and 302 sub-certification processes with simple electronic forms. Implement automated workflows to route changes or escalate issues. Link policies to related compliance content, such as regulatory frameworks or internal controls.
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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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    EasyAudit

    EasyAudit

    EasyAudit

    EasyAudit.ai is a cutting-edge AI-powered auditing platform designed to help businesses and organizations streamline their audit processes, ensure compliance, and detect risks quickly and efficiently. Leveraging advanced artificial intelligence and machine learning algorithms, EasyAudit.ai automates the traditionally manual and time-consuming aspects of auditing, such as data analysis, document review, and error detection, significantly reducing human effort and improving accuracy. It offers real-time insights and risk assessments, enabling companies to identify potential issues before they escalate. Its intuitive interface allows users to upload financial data, contracts, and other documentation, which the AI reviews for inconsistencies, regulatory compliance, and red flags. EasyAudit.ai also provides customizable audit workflows, making it adaptable to various industries, including finance, healthcare, legal, and corporate sectors.