Alternatives to QbDVision
Compare QbDVision alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to QbDVision in 2026. Compare features, ratings, user reviews, pricing, and more from QbDVision competitors and alternatives in order to make an informed decision for your business.
-
1
Lockbox LIMS
Third Wave Analytics
A sample tracking, test result capture, and inventory management cloud LIMS for life science research, biotech/NGS, and industrial QC labs. Includes regulatory support for CLIA, HIPAA, Part 11, and ISO 17025. Nothing is more critical to a lab’s success than the quality, security, and traceability of samples. The Lockbox LIMS system provides robust sample management functionality to laboratory professionals, giving them full visibility on every aspect of a sample’s journey, from accessioning to long-term storage. LIMS analysis is about more than just tracking results- Lockbox’s multi-layered sample storage and location management functionality allows you to define your lab’s storage framework using a variety of location options: rooms, storage units, shelves, racks, boxes, and positions. -
2
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. -
3
IQVIA
IQVIA
Thousands of organizations around the world trust IQVIA to speed drug development, ensure product quality and safety, improve commercial effectiveness, get the right treatments to patients, improve access to and delivery of healthcare, and ultimately drive better health outcomes. Reimagine clinical development by intelligently connecting data, technology, and analytics to optimize your trials. The result? Faster decision making and reduced risk so you can deliver life-changing therapies faster. With a foundation in data, advanced analytics, and expert insight, IQVIA brings specialized capabilities to customers across the healthcare ecosystem. Read and watch the latest from IQVIA data scientists, doctors, researchers, and other subject matter experts on the topics that matter to you. From industry trends to how we are applying our capabilities to help, you can find it here. -
4
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. -
5
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. -
6
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.
-
7
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. -
8
Pluto
Pluto Biosciences
Since its founding in 2021 from the Wyss Institute at Harvard University, Pluto has become a trusted partner of life sciences organizations around the country ranging from biotech start-ups to public biopharma companies. Our cloud-based platform gives scientists the ability to manage all of their data, run bioinformatics analyses, and create interactive and publication-quality visualizations. The platform is currently being used for a wide variety of biological applications, from preclinical / translational science research, to cell and gene therapies, drug discovery and development, to clinical research. -
9
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. -
10
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. -
11
IDBS Polar
IDBS
Meet IDBS Polar, the world’s first BioPharma Lifecycle Management (BPLM) platform, eliminating repetitive manual tasks, allowing you to efficiently execute your processes while curating the data you need to accelerate time to market by tackling the biggest challenges in process design, optimization, scale-up, and technology transfer. Interactive data analytics applications, such as bioreactor comparison designed specifically for biopharma development scientists. IDBS Polar is a platform that securely manages drug progression in contexts of workflow, integration, and insight. Workflows designed to simplify the BioPharma Lifecycle with process-aware planning, design, and execution of end-to-end bioprocess and analytical unit operations. Integrations that bring meaning to your data. Rapid integration into your development ecosystem, enabling automation and curating a process-centric data backbone. -
12
Sapio LIMS
Sapio Sciences
Sapio Sciences delivers the Sapio Platform, an agentic AI lab informatics platform that makes life in the lab easier and more productive for scientists. The unified, configurable, low code and scalable environment brings together Sapio LIMS, the market’s most advanced and flexible LIMS for automating research, diagnostics and manufacturing, Sapio ELaiN, the third generation AI lab notebook and scientific co scientist, and Sapio Scientific Data Cloud, the scientific data unification solution with built in organization, search, charting, tools and AI. Biopharma R&D, biotech, CRO and clinical diagnostics organizations use Sapio to run complex workflows and keep samples, experiments and data connected in one place instead of juggling disconnected systems. -
13
Sapio Sciences
Sapio Sciences
Sapio Sciences delivers the Sapio Platform, an agentic AI lab informatics platform that makes life in the lab easier and more productive for scientists. The unified, configurable, low code and scalable environment brings together Sapio LIMS, the market’s most advanced and flexible LIMS for automating research, diagnostics and manufacturing, Sapio ELaiN, the third generation AI lab notebook and scientific co scientist, and Sapio Scientific Data Cloud, the scientific data unification solution with built in organization, search, charting, tools and AI. Biopharma R&D, biotech, CRO and clinical diagnostics organizations use Sapio to run complex workflows and keep samples, experiments and data connected in one place instead of juggling disconnected systems. -
14
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. -
15
Cerella
Optibrium
Proven AI-powered drug discovery. Cerella creates new value from your drug discovery data, revealing hidden insights into the best compounds and most valuable experiments for your project. It makes confident predictions, accurately filling in missing values, especially for expensive downstream experiments that can’t be predicted by other methods. This enables you to do more, even with sparse, limited data sets. -
16
AmpleLogic Document Management
AmpleLogic
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. -
17
Kivo
Kivo
Kivo is a better way to work for sponsors and CROs, offering an affordable document and process management system that helps life sciences teams get work done in one intuitive, compliant workspace. It brings DMS, RIM, QMS, eTMF, and eCTD capabilities together so pharmaceutical, biotech, medical device, and biologics teams can manage regulated documents, quality activities, clinical trial files, regulatory submissions, and process workflows without disconnected tools. Kivo’s Document Management System provides one place for controlled documents, process automation, project management, corporate documents, and diligence readiness, with centralized storage, version control, collaboration, audit trails, search, workflow automation, and Part 11-compliant e-signatures. Its RIM system supports correspondence, project management, submission building, publishing handoff, eCTD viewing, dossier management, agency interactions, health authority commitments, etc.Starting Price: $1,800 per month -
18
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. -
19
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.
-
20
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 -
21
comForte
comForte
Integrated data-centric security is part of your overall business strategy. Unfortunately, traditional controls focus on the border around the data, keeping data siloed and sometimes unusable. This approach is incompatible with business drivers such as data analytics and automated AI/ML workflows. Data-centric security fundamentally changes the way you protect, control, audit, and work with your most sensitive business data by tokenizing sensitive data elements and preserving its original format. An effective data-centric security solution is broader than just data protection. A comprehensive platform for both data discovery and protection that can scale as an organization grows. -
22
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 -
23
Statim
Statim
Statim (Latin for "immediately") is the unified pharmaceutical intelligence tool built for modern clinical practice. It eliminates the friction of fragmented drug data by consolidating prescribing info, safety analysis, and clinical trial evidence into a single, reliable workspace. Statim's "Smart Search" feature empowers healthcare professionals with immediate, data-driven decisions through advanced FDA adverse event analysis and peer reviewed published articles. Access all critical drug intelligence quickly and securely—it's free and does not handle patient data. Who is Statim for: + Physician + Medical Resident / Fellow + Nurse Practitioner + Physician Assistant + Pharmacist + Pharmacy Resident + Registered Nurse + Medical Assistant + Healthcare Administrator + Formulary / Payer Specialist + Medical Student + Pharmacy Student + Nursing Student + Researcher + Patient + CaregiverStarting Price: Free -
24
Close-Up CRM
Close-Up International
Close-Up International is a leading provider of market data and technology solutions tailored for the pharmaceutical and life sciences industry. With over 55 years of experience, Close-Up supports more than 650 clients across 50 countries by delivering high-quality, certified data and innovative analytic tools. Their solutions help companies assess market potential, target healthcare professionals, and optimize product launches. The platform integrates market, prescription, and sales data with CRM capabilities for a comprehensive view of market dynamics. Close-Up’s offerings are designed to improve decision-making and strengthen relationships between pharmaceutical companies and healthcare providers. They emphasize data security, holding ISO 9001 and 27001 certifications. -
25
LabCollector LIMS/ELN
AgileBio
AgileBio develops and markets the innovative and flexible LIMS solution "LabCollector". Over the past 24 years, AgileBio has continued to develop LabCollector as an innovative solution to provide collaboration and processing tools that improve laboratory productivity and traceability. AgileBio combines the skills of laboratory experts (with PhDs) and software developers to continually bring new features in close dialogue with laboratory expectations. AgileBio has served over 1200 labs worldwide. We propose IT solutions and hardware (scanners, labels, printers, etc.) for labs in R&D, clinical trials, analytical, medical, quality control, GxP, and for various industries (biotech, pharma, food and beverage, etc.). LabCollector is an all-in-one flexible and intuitive LIMS/LIS/ELN software, built to organize, centralize and track reagents, samples, tests, experiments, workflows, lab data and processes, with full ISO/FDA compliance.Starting Price: 400€/user/year -
26
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. -
27
Reliant AI
Reliant AI
Accuracy, speed, confidence. Introducing generative AI to commercial biopharma. Simplify the labor-intensive process of collecting, organizing, and inspecting vast amounts of complex data. Get straight to decision-critical insights with 100% confidence, every time. With our AI-powered data manipulation and verification platform, you'll never lose track of your workstreams again. Gather, refine, and check your data, all in one place. Search public and private databases by key drug characteristics. Segment drugs and trials by detailed patient profiles. Extract the data you need in plain English. Support your findings by linking answers back to their source. Focus your time and energy on synthesizing high-quality outputs from data rather than menially sifting through it. Our specialized LLMs enable researchers to perform asset scans 4.8x faster than by hand. We index over 38M scientific publications, conference abstracts, and clinical trials. All the data you need, when you need it. -
28
Chemaxon
Chemaxon
Working alongside both our in-house chemists and biologists, and our clients, we build products that deliver outstanding performance and scientific understanding. Chemaxon's product portfolio offers out-of-the-box solutions for scientists, back-end tools for IT professionals, components to add extra functionality, and integrations to make our technology available from 3rd party software like Microsoft Excel or KNIME. Trusted by over one million active users, Chemaxon is renowned for industry-leading software supporting scientific discovery with calculation, search and drawing tools. Our applications are widely used in life sciences R&D and education. We work with a variety of industries, counting most major pharmaceutical companies among our clients. Our offices are located in Budapest, Basel, Boston and San Diego, with distributors around the world. -
29
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. -
30
Skyland PIMS
IDBS
End-to-end Product and Process Data Management. Skyland PIMS® provides emerging & global drug sponsors and CMOs a collaborative workspace to manage critical development, manufacturing and quality data. Our cloud-based, validatable software allows for fast deployment and low TCO. Maintain data content, understanding, and control across the supply chain. Faster and more efficient scale-ups, tech transfers, and commercial releases. Capture batch data and access summary dashboards for data monitoring, release status, analysis and reporting. Manage product and process specifications and target control limits. Easily create an audit trail. Automatically integrate Batch and Limits data to produce process analysis and control charts. Fulfill CPV/APR reporting requirements. Persistent product and process data library for data transparency and integrity across global networks. Streamline product and process data management throughout the product lifecycle and supply chain. -
31
Reshape
Reshape
Reshape Biotech delivers a robotics-and-AI-powered automation platform for microbiology laboratories that transforms manual plate-based assays into scalable, data-rich, reproducible workflows. Its core products, including a “Smart Incubator,” a high-throughput imaging device, and a cloud-based “Discovery Platform,” automatically capture high-resolution images of Petri dishes or microtiter plates during incubation, then upload them to the cloud for real-time AI analysis. It can accurately process colony counting, radial growth, fluorescence, turbidity, color assays, seed-germination phenotypes, antagonistic assays, and other microbial or cell-based readouts, eliminating time-consuming manual observation and reducing errors. By storing every experiment and dataset in a unified, searchable workspace, Reshape enables teams to compare results across experiments, collaborate across labs, and ensure standardization and reproducibility regardless of scale. -
32
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. -
33
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.
-
34
RegDocs Connect
Montrium
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 -
35
ZAIDYN
ZS
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. -
36
ExtendMed
ExtendMed
Engage healthcare stakeholders to solicit insights, advance clinical research, and share online learning. Learn how partnering with ExtendMed will maximize the frequency and value of your interactions at a third of the cost of traditional approaches. Let us help you maximize your reach and impact. We have 20 years of experience working with pharmaceutical companies, agencies, and associations to provide scientific, marketing, education, and training solutions using our Health Expert Connect platform including: - Hosting virtual advisory boards - Speaker bureau management: contracting, training, logistics, closeout, Sunshine reporting - Smartphone event engagement: sign-in, slides, polling, surveys, assessments, follow-up - Online product theaters and satellite symposia -
37
ELOprofessional
Ovitas
When it’s in ELO – you can find it, access it and use it. Document management happens in your functional areas—finance, accounting, procurement, human resources, and operations—you need a solution that works across functions, no matter what industry you’re in. Your document management solution should be easy to use but also include core, document-centric functionality. Capture your business documents via scanning or automated import, then tag and classify your documents using smart, automated workflows. Document management is a process, so you need a system that can automate your document-centric business processes easily with custom workflows. Your employees manage thousands of business records. Custom metadata let them easily classify, index and manage documents in a logical and controlled way. -
38
StayinFront TouchRx
StayinFront
StayinFront’s CRM solutions has been helping pharmaceutical companies succeed for over 20 years. TouchRx features a configurable solution that meets the needs of pharmaceutical companies, and is backed by an experienced and responsive support team to help companies maximize their ability to do more, know more and sell more. The highly regulated pharmaceutical industry requires specific processes be followed by field teams when promoting products. It is often assumed that these regulations tend to lead to a cookie cutter approach by CRM partners that provide solutions for field teams. Complying with regulations such as sampling and product promotion are critical, but what is offered in addition to these core features may determine the level of success you will have. -
39
SolarWinds Task Factory
SolarWinds
Developer teams building data-centric applications on the Microsoft data platform face challenges when using SQL Server Integration Services (SSIS) for data extract, load, and processing (ETL) tasks. Ensuring an efficient ETL design is one of the most important—but often overlooked—aspects of ensuring a high-performing data-centric application. If your SSIS packages aren't performing efficiently, you're potentially wasting development resources, processing power, and hardware resources. -
40
AmpleLogic Learning Management System
AmpleLogic
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. -
41
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. -
42
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. -
43
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 -
44
Seqera
Seqera
Seqera is a bioinformatics platform developed by the creators of Nextflow, designed to streamline and enhance the management of scientific data analysis workflows. It offers a comprehensive suite of tools, including the Seqera Platform for orchestrating scalable data pipelines, Seqera Pipelines for accessing a curated collection of open source workflows, Seqera Containers for simplifying container management, and Seqera Studios for interactive data analysis environments. It supports seamless integration with various cloud and on-premises infrastructures, ensuring reproducibility and compliance in scientific research. Integrate Seqera into existing on-premises systems and cloud platforms like AWS, GCP, and Azure, with no forced migrations. Maintain full control over data residency and scale globally, without compromising security or performance. -
45
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. -
46
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. -
47
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. -
48
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!Starting Price: $1000 -
49
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.Starting Price: $35.00/month/user -
50
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.
