Alternatives to Scientist.com
Compare Scientist.com alternatives for your business or organization using the curated list below. SourceForge ranks the best alternatives to Scientist.com in 2026. Compare features, ratings, user reviews, pricing, and more from Scientist.com competitors and alternatives in order to make an informed decision for your business.
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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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Ketch
Ketch
Complying with them is expensive. As soon as you’ve responded to one regulation, another one pops up. Consumers are mistrustful for good reason. Avoid complexity and use data to grow, or comply and stagnate. Simple to deploy. Simple to use. Simple to adapt to changing regulations and business conditions. Impossible to beat, with all the capabilities you need to build trust, collapse the costs of compliance, and harness data for top-line growth and core operations. Ketch is redefining how organizations satisfy their data privacy and governance needs with the most adaptable data control platform available. No more whack-a-mole. Set-it-and-forget-it, perfect compliance with continuous updating of data privacy laws and turnkey templates for policy-managed governance. Meet the intricacies of any data law or policy with data control at the level of individual people, partners, and purposes (“use my data for analytics but not targeting”). -
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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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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. -
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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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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 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. -
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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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Prendio For Biotech
Prendio
Unlike other eProcurement solutions, Prendio was built specifically for biotech. We’ve designed a simple, streamlined, and affordable procure-to-pay solution that improves efficiency and decreases the administrative burden, speeding research and reducing development cycle time. Our intuitive functionality helps you easily create and save carts from all of your favorite suppliers. View order history and status and receive convenient notifications right on your dashboard. Place orders by browsing the catalog and comparing item ratings, or take advantage of our convenient punchouts. Save carts as templates to make reordering a breeze. We provide free, comprehensive punchouts custom-built for your company. Our robust, industry-leading supplier partner portfolio gives you broad access to this automated purchasing solution. By matching invoices, packing slips, and POs digitally, finance can be confident that they are only paying for goods and services that have been received. -
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Supply Chain Wizard Digital Factory
Supply Chain Wizard
Digital Logbook, Digitize room logs to save time while complying to GMP. Industry Challenge. At Pharmaceutical sites, all activities should be recorded to logbooks to comply with GMP regulations. Having manual logs such as written or excel sheet logbooks are of common practice. This limits the further analysis of the logs. Maintaining the logbooks become too costly when manual methods are used and security concerns arise. What you get? User-friendly, flexible and scalable architecture. Digitize all room logs and forms capturing activities on the factory floor. Access your data easily and remotely at all times. Improve security and quality by using personal digital signatures. Comply with GMP regulations Immutable records with optional blockchain technology. How does it work? Line operators log each activity / task with a few clicks or touch . Multiple levels of security ensure the GMP compliance of the logbook. Flexible workflows match your entry and template approval process. -
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Termly
Termly
Trusted by over 140,000 businesses, Termly’s compliance solutions can help you stay up to date and compliant in an ever-changing ecosystem of privacy laws like the GDPR, CCPA, ePrivacy Regulation, and many more. Policies created by our state-of-the-art software are tailor-made to fit the unique needs of your business. Our cookie consent manager can help you comply with complex consent laws like the GDPR and ePrivacy Directive. Compliance with international laws like the GDPR, CCPA, and ePrivacy Regulation made fast and easy. Running a business requires you to comply with a wide variety of laws, rules, and service provider guidelines. It’s a hassle and a risk trying to adhere to all of these regulations on your own. Termly can help ease the burden of legal compliance and give you peace of mind.Starting Price: $10 per month -
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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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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. -
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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)comStarting Price: $10/user/month -
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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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ModelOp
ModelOp
ModelOp is the leading AI governance software that helps enterprises safeguard all AI initiatives, including generative AI, Large Language Models (LLMs), in-house, third-party vendors, embedded systems, etc., without stifling innovation. Corporate boards and C‑suites are demanding the rapid adoption of generative AI but face financial, regulatory, security, privacy, ethical, and brand risks. Global, federal, state, and local-level governments are moving quickly to implement AI regulations and oversight, forcing enterprises to urgently prepare for and comply with rules designed to prevent AI from going wrong. Connect with AI Governance experts to stay informed about market trends, regulations, news, research, opinions, and insights to help you balance the risks and rewards of enterprise AI. ModelOp Center keeps organizations safe and gives peace of mind to all stakeholders. Streamline reporting, monitoring, and compliance adherence across the enterprise. -
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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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Sword Quality Manager
Sword GRC
For over 10 years Sword Quality Manager has been instrumental in helping international organizations from manufacturing, pharmaceutical, FMCG and other quality conscious industry sectors to comply with standards such as ISO9001, safety and hygiene regulations, promote safety in the workplace and streamline quality processes efficiently, adding to bottom line profitability. -
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Pier Finance
Pier
Increase transaction volume and order size on your marketplace with an embedded lending layer. Eliminate legacy systems of spreadsheets, calendars, and file storage. Save time researching requirements and submitting filings. Reduce risks of license gaps and missed renewals. Access up-to-date requirements from the reference database. Built-in compliance guard rails to comply with state & federal regulations. Check your loan parameters before making offers to your users. Stay up to date on regulatory changes affecting your planning. Assess your compliance training needs based on state and federal regulations, company goals and third-party partnership requirements. Build and automate your compliance training program, customized to your needs. -
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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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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 -
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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. -
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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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COMPLY
COMPLY
COMPLY is a modern compliance management platform built specifically for financial services firms. It centralizes regulatory requirements, automates manual workflows, and helps firms stay ahead of evolving regulations. By uniting data, solutions, services, and education, COMPLY empowers compliance teams to scale operations efficiently while reducing regulatory risk. The platform supports a range of functions—from regulatory filings and policy reviews to managed services—acting as an extension of your team. Designed for private funds, broker-dealers, wealth managers, investment banks, and more, COMPLY ensures firms operate in the best interest of investors and clients. With its easy-to-use interface and expert support, COMPLY delivers confidence, clarity, and control over compliance programs. -
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Scout
Scout Data
Scout Data's KOL management software is a robust platform designed to optimize Key Opinion Leader (KOL) engagement for the pharmaceutical industry. It offers a comprehensive KOL database, advanced profiling, engagement planning, and consent management. The platform includes powerful data analytics, reporting capabilities, and a calendar module, ensuring efficient tracking of KOL activities while promoting compliance with company policies. Customizable to the needs of each client, the software supports improved interaction with KOLs and enables tailored reporting and strategic planning. This tool is widely used across the pharmaceutical sector to streamline KOL management and enhance the effectiveness of engagement strategies. -
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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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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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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. -
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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. -
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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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Labelmaster
Labelmaster
For more than five decades, Labelmaster has been the go-to source for companies, big and small, to navigate and comply with the complex, ever-changing regulations that govern dangerous goods and hazardous materials. From hazmat labels and UN-certified packaging, hazmat placards, and regulatory publications, to advanced technology and regulatory training, Labelmaster’s comprehensive offering of industry-leading software, products, and services helps customers remain compliant with all dangerous goods regulations, mitigate risk, and maintain smooth, safe operations. Labelmaster's dedication to supporting its customers' operational and compliance needs is enhanced through its unmatched industry expertise and consulting services, which serve as a valuable resource for customers to answer difficult and commonplace regulatory questions. Whether you're shipping hazardous materials by land, air, or sea, Labelmaster is your partner in keeping your business ahead of regulations. -
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AML Accelerate
Financial Crimes Consulting
AML Accelerate is a cloud-based counter-terrorism financing and AML risk assessment platform designed by experts and is tailored to over 30 financial and non-financial industry sectors. Money laundering and terrorism financing laws apply to millions of organisations of all sizes across different industry sectors and geographies. Complying with increasing regulations can be complex and costly, AML Accelerate is an easy-to-use platform designed by experts to guide you to compliance, saving you time and money. Tailored to over 30 industry sectors and country-specific laws, it provides peace of mind that mandatory anti money laundering regulations are being met and your AML risk being managed. Complying with increasing anti money laundering risk regulations can be complex and costly, with experts in short supply. Designed by experts, so you don’t need to be one. Meet mandatory regulatory compliance requirements for audits. -
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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 -
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Truven
Merative
Truven, a part of Merative, offers a comprehensive suite of healthcare analytics and member engagement solutions aimed at enhancing health and financial outcomes. Their offerings include information services, analytic tools, benchmarks, research, and consulting services tailored for various healthcare organizations. With over 40 years of experience, Truven is trusted by leading health plans, employers, benefits advisors, government agencies, providers, pharmaceuticals, biotech, and medical device companies. Their solutions are designed to support patient safety, streamline workflows, and provide actionable insights to improve healthcare delivery and management. -
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Aclid
Aclid
Rich threat assessments and risk profiles delivered in seconds for hundreds of thousands of base pairs. Monitor orders at checkout and prevent misuse. Automatic verification of licenses and registrations, biosafety guidelines, and legitimate use. Save time going back-and-forth with your customers. We complete all compliance checks at checkout. By using Aclid, you can prevent order cancellations and delays from lost emails and slow responses. Our platform streamlines the compliance process by managing customer follow-up. Respond to fewer false alarms with all your data in one place. Let us manage your biosecurity process while you grow your business. We stay up to date on new regulations, guidelines, and research. With Aclid you get a powerful platform that manages the entire process and in-house support to guide you along the way. -
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PORT.im
PORT.im
Privacy Center is the new way to communicate privacy, comply with the regulations and build trust in your brand. From your website to your compliance records, PORT.im is connected from end-to-end so everything works together making your business safer, compliant and more trusted. Compliance with CCPA, CalOPPA, GDPR and more. We constantly monitor the world's leading privacy regulations and update our policies to ensure you comply with the regulations. A groundbreakingly simple approach to privacy. PORT.im makes it simple to comply with the regulations by generating a Privacy Center that accurately reflects your business. Show you respect the privacy of your customers by making it simple for them to read and understand your privacy information. PORT.im streamlines privacy management making the complex regulations simple and difficult tasks easy. Explore Privacy Center, or create an account instantly and publish your free Privacy Center.Starting Price: $40 per month -
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Simplify how you manage and comply with data protection and privacy regulations around the world. Evaluate organizational maturity and establish a security and privacy governance model in accordance with requirements and best practices. Embed data-driven assessments within business processes to meet organizational privacy requirements. Facilitate self-service requests and automate the review and response process to enable better privacy management practices. Identify security and privacy risks and create a remediation plan to meet objectives and comply with regulatory requirements. Deploy and manage maturity assessments with flexible and configurable templates. Follow the setup instructions so you can start running your SAP software quickly and confidently. Find out how you can seamlessly integrate SAP Privacy Governance with your existing IT landscape.Starting Price: $43.92 per year
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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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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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newLab
newLab
newLab Cloud is an AI-ready lab management platform built on ServiceNow. It helps biotech, pharmaceutical, and research organizations streamline workflows, manage laboratory equipment, and automate compliance processes. Designed for modern R&D environments, it offers equipment tracking, document management, workflow automation, and audit trails in one secure, cloud-based platform. With integrations for ServiceNow, newLab Cloud connects lab and IT operations to improve collaboration, ensure data integrity, and accelerate innovation. -
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Kaizen
Kaizen
Transform how you meet your compliance and regulatory reporting obligations. We are a team of regulatory experts, technology developers, and data engineers focused on improving data quality and creating new solutions to the complex challenges of regulation. Our award-winning products help clients from across the financial services industry, from boutique asset management firms to tier-one banks, meet the demands of regulators. Get accurate, complete, and timely regulatory reporting. Search, share, and manage regulation on one digital platform. Automated shareholding disclosure monitoring and reporting. A holistic approach for managing market abuse and misconduct. Reduce regulatory risk with automated research management. Accredited training for a wide range of regulatory reporting regimes. We are regulatory and data specialists on a mission to revolutionize the way people work with compliance and regulation. -
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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. -
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QX ComplyRite
QX Global
Recruitment companies often end up spending significant time & resources in making registrations and ensuring compliance. Following age-old, legacy processes for these activities can not only lead to increased costs, but also hamper the overall candidate experience. QX ComplyRite is a future-ready platform that streamlines the process of maintaining compliance with required regulations. A tool uniquely designed by recruiters for recruiters, QX ComplyRite helps organizations ensure that their employees/candidates stay complaint as per the required regulations and standards. Allows users to quickly deliver important compliance updates to multiple candidates in just one click. Optimizes the recruitment process by centralizing administration, whilst boosting business visibility. -
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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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Cookie Information
Cookie Information
Streamline the way you collect consent across your websites and apps without ever worrying again about complying with global privacy regulations (such as GDPR, ePrivacy, and CCPA). Eliminate the risk of fines by demonstrating full compliance with international data protection regulations with reliable and scalable consent collection on your websites and apps. Maximize revenue and build user trust by proactively monitoring and optimizing consent rates across your digital portfolio. Provide your marketing team with compliant data for analytics and ads. Collect anonymized conversion data with Google Consent Mode and protect your brand reputation by eliminating the risk of data regulation fines. Comply with international privacy regulations and national interpretations. Equip your marketing and IT teams with tools that ensure your data protection compliance. Track and report on compliance and data breaches across all your websites and apps.Starting Price: €10 per month -
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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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Reva QMS
Reva Solutions
Reva QMS is a software-based Quality Management System. Our solution is designed to help organizations collect, organize, manage, and report on their business-critical documents while aligning their business processes to comply with relevant industry standards, specifications, laws, and regulations. Specifically designed for highly regulated industries, Reva QMS helps organizations automate and streamline their paper processes for increased efficiency and regulatory compliance. It provides a comprehensive set of out-of-the-box functions and capabilities specifically designed for highly regulated industries to help them achieve greater operational transparency and comply with rules and regulations, policies, best practices, and industry standards. It provides an easy-to-use browser interface that allows users to manage critical business processes easily and in a simple manner. -
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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. -
49
ithikios
DIGITAL PRODUCTS DEVELOPMENT
The simple, secure and easiest-to-install whistleblowing channel for small and medium enterprises. Create an anonymous whistleblowing channel to indentify problems inside organizations and comply with the law. A key element for penal compliance, labour compliance, whistleblowing European directive, ISO 37301 and UNE 19600. The channel for anonymous complaints to meet the requirements of criminal, labor and European regulatory compliance of "whistleblowing". Obligatory for companies with more than 50 employees. Simple and in the cloud, easy to use. Sets up in minutes and ready to go. No need for technicians or infrastructure. Install and comply with regulations. Information security and adapted to Spanish data protection regulations. Transparency with your employees, customers and suppliers. Improve with all the contributions of your ecosystem and achieve excellence.Starting Price: €19 per month -
50
Nova-QMS
Novatek International
Maintaining consistent product quality and quality processes can be challenging in today’s pharmaceutical manufacturing environments. Regulated industries such as the Pharmaceutical, Biotech and Life Sciences are required to maintain Good Manufacturing Practices (GMP) to meet regulatory requirements. Not only do you need to meet GMP requirements you must also be able to prove this. Using paper-based forms, disconnected systems, or manual processes to manage, track and report on quality issues and actions does not provide effective solutions for implementing harmonized, integrated quality management processes, which follow industry best practices.
