Alternatives to Scilife

Qualio is a one-stop solution for quality and compliance management. It's ideal for growing companies in healthcare and life sciences. Qualio is reliable, affordable and easy to use. It helps companies build life-saving products faster and achieve 100% ISO, GxP and FDA compliance. Qualio makes it easy for companies to manage document control, training and NCRs, audits as well as suppliers, complaints, and other tasks in one platform.

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

A cloud LIMS that tracks samples, tests results, and manages inventory for life science research, industrial QC labs, and biotech/NGS. Includes regulatory support for CLIA and HIPAA, Part 11 and ISO 17025. The quality, security, traceability, and traceability for samples is crucial to a lab's success. Laboratory professionals can use the Lockbox LIMS system to manage their samples. They have full visibility of every step of the sample's journey from accession to long-term storage. LIMS analysis is more than just tracking results. Lockbox's multilayered sample storage and location management functionality lets you define your lab's storage structure using a variety location options: rooms and storage units, shelves and racks, boxes and boxes.

QBench allows you to keep track of all your samples and where they are located in the workflow using a single system. QBench eliminates the need for spreadsheets, shared folders in the network, and paper-based tracking systems. You can view hundreds of PDF reports/COAs before publishing or emailing. You can generate barcodes and create labels that you can customize for your samples. Compatible with standard printers and scanners. QBench's billing module allows you to create and send invoices right from the system. You can see counts and latencies for different data types in QBench. This includes metrics like turnaround time, sample counts per test, sample delay, and many others. QBench makes it easy for you to gather the data your lab needs for the assays you perform.

SimplerQMS offers a cloud-based Quality Management Software, specifically designed for the Life Science industry. SimplerQMS helps ensure compliance with various regulatory requirements, including FDA 21 CFR Part 11, EU Annex 11, GxP, cGMP, GAMP 5, GDPR, EU IVDR & EU MDR, ISO 13485:2016, 21 CFR Part 820, and ICH Q10, among others. The system is fully validated according to GAMP5. The system offers a range of Life Science QMS modules such as Document Control, Change Control, Training Management, Supplier Management, Complaints Management, Non-Conformance and Deviation Management, CAPA Management, Audit Management, Technical Documentation Management, Risk Management, Quality KPIs and more. SimplerQMS integrates with Microsoft Office and allows users to work with documents in applications such as Word, PowerPoint, and Excel. Overall, SimplerQMS delivers efficient, paperless workflows that align with the compliance requirements of the Life Science industry.

Dot Compliance offers the industry's first ready to use Quality Management Solution powered by the Salesforce.com platform. The Dot Compliance solution includes an extensive set of off-the-shelf ready eQMS and compliance pre-configured processes, enabling customers to deploy quickly and cost effectively. Dot Compliance ready to use solutions include full project validation services and product validation packages. Dot Compliance offers the industry’s most cost-effective quality and compliance management solution available, allowing users to quickly deploy flexible and scalable solutions. Automate core quality processes such as Document Management, Training Management, CAPA, Audits, Customer Complaints, Change Management, Supplier Quality, and more. Our solution is fully configurable and offers seamless integration abilities, with easy adaptation and implementation of customer’s specific requirements.

Unify quality processes with QT9's all-in-one cloud-based QMS Software Suite. QT9 QMS is a user-friendly quality management software that includes 25+ modules with unlimited scalability. Automate ISO & FDA Compliance with email alerts, To Do lists and FDA 21 CFR Part 11 Compliant Electronic Approvals. QT9 QMS enables Life Sciences, Biotechnology Companies, Medical Device Manufacturers and Pharmaceutical Companies to digitally transform operations. Get real-time status updates and visualize quality metrics up-to-the-minute. QT9 QMS comes with built-in document control, revision-level controls, corrective actions (CAPAs), Nonconforming products and more. Advance product releases with Deviation Management, Engineering Change Orders, FMEA, Inspection Management Modules Included. Go paperless & put time-consuming tasks on autopilot. QT9 QMS comes ready-to-use. Get a free product tour! Start a Free Trial. Visit QT9qms.com

It is difficult to make data available and actionable when a manufacturing site has many processes. As operations grow, it is becoming more difficult to comply with safety, quality, and environmental regulations. Manufacturing is built on predictability and reliability. Manufacturing by nature is all in the execution of established processes. TenForce was built from the feedback of our clients to map the operational reality in a plant.

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

Natively built and operated on the Salesforce platform, QHSE is the fastest growing Enterprise Quality, Health and Safety Management System. Unified QHSE solutions combine EQMS with EHS to help customers of all sizes deliver high quality products and services in a safe and sustainable manner. They reduce risk, inefficiencies, and inefficiencies, while protecting their customers, employees, and brand.

Ensuring uniform product quality and robust quality management procedures poses significant challenges in the current landscape of pharmaceutical manufacturing. Industries governed by strict regulations, including Pharmaceuticals, Biotechnology, and Life Sciences, must adhere to Good Manufacturing Practices (GMP) to comply with legal standards. Beyond merely fulfilling GMP obligations, it is essential to provide evidence of compliance. Relying on paper forms, isolated systems, or manual procedures to oversee, monitor, and document quality issues and responses fails to offer effective solutions for establishing cohesive and integrated quality management practices that align with industry standards. Consequently, organizations must seek more advanced and automated systems to enhance their quality assurance efforts and streamline compliance.

Cloud-based Enterprise Quality Management Software tailored for the life sciences sector is essential in navigating today’s intricate operational landscape. With technology at the forefront, it ensures that quality assurance teams are promptly informed of issues as they arise, fostering a culture of proactive management. By gaining a clear view of the quality management system's performance alongside operational conditions, organizations can significantly reduce risks and avoid expensive delays. Montrium has crafted its Enterprise Quality Management System (EQMS) specifically to help life science companies confront their quality management challenges directly, particularly in content management. Our SharePoint QMS modules are designed for flexibility; they can function independently or as part of a cohesive quality management system. These modules are accessible through our Montrium Connect Platform and can be implemented either on-premise or via cloud solutions, making them ideal for pharmaceutical firms, contract manufacturing organizations, and medical device companies. Each component is meticulously built to ensure compliance with Good Manufacturing Practices (GMP) and Good Clinical Practices (GCP), thereby supporting organizations in maintaining the highest quality standards. Ultimately, this comprehensive approach not only enhances efficiency but also strengthens the overall integrity of the quality management process.

Agatha provides a comprehensive range of cloud-based solutions specifically designed for the life sciences sector, facilitating the centralized oversight of documents and processes related to clinical operations, quality assurance, regulatory compliance, and training activities. This platform caters to the workflows of biotech firms, pharmaceutical companies, medical device manufacturers, and contract research organizations by offering various modules, including eTMF (Inspection-Ready Master Trial File), Remote ISF (Investigator Site File) management, and tools for creating and approving standard operating procedures (SOPs) as well as managing quality documents related to CAPAs, deviations, and change controls. Additionally, Agatha enhances regulatory document handling, ensuring smooth document creation, review, approval, storage, and sharing within a single cohesive system. By promoting a paperless approach, it alleviates administrative burdens and bolsters data security, while being constructed on a global-compliance framework that meets critical standards such as 21 CFR Part 11, GDPR, and EU Annex 11. Ultimately, Agatha empowers life sciences organizations to optimize their operations and maintain compliance with industry regulations more efficiently.

Cloud-first ERP solutions are specifically designed to meet the needs of life science companies. Merit for Life Science is a cloud-first ERP system that has been expertly crafted for manufacturers in the biotech, pharmaceutical, and medical device sectors. It enhances Dynamics 365 finance and operations, providing a seamless connection across your entire organization. This system effectively aligns resource qualifications with production needs, while also overseeing vendor relationships in procurement to ensure compliance with quality standards during manufacturing. By offering your life science organization enhanced visibility and transparency, it supports the delivery of safe and innovative products, among other benefits. Recognizing that each organization has its own distinct requirements, we are committed to understanding those needs. Explore the comprehensive solutions we provide, which are tailored to satisfy the stringent demands of the pharma, biotech, and medical device industries. Additionally, our system aids in refining your decision-making processes through dependable and auditable accounting practices, while also establishing robust financial reporting standards for acquired entities or preparing your organization for acquisition, ensuring you are always ready for the next step in your growth journey.

ZenQMS improves the quality compliance profiles life sciences companies through a cloud-based platform. It is purpose-built to facilitate document collaboration, control, training, issues management, audits, and change management. ZenQMS is a team of technology and quality leaders who share the common goal of making quality management a business imperative.

The AssurX platform is a powerful software platform for enterprise quality management (EQMS) and regulatory compliance to reliably communicate and coordinate information, documentation, and activities. AssurX allows regulated businesses to quickly identify and control quality issues and risk exposure to avoid quality or noncompliance problems while improving workflow. AssurX QMS software is uniquely configurable to fit any established or dynamic business requirements. The system creates an electronic workflow of tasks, alerts, escalations, and approvals that can be automated to the desired level, mapping precisely to real-world operations. No other system is easier to deploy, configure, and modify. AssurX solutions integrate seamlessly to create a connected quality system. Solutions include audit management, corrective actions, training management, compliant management, document management, change control, risk management, EHS incident management, and more.

Enhance quality and ensure GxP compliance through Vault QMS, which integrates established best practices and automated workflows to connect all stakeholders, including pharmaceutical and biotech firms, contract manufacturers, and suppliers, into cohesive quality processes for improved oversight and control. This system facilitates seamless collaboration among various departments, sites, contract manufacturers, suppliers, and testing labs, promoting a culture of continuous quality enhancement. By leveraging automated workflows, organizations can achieve greater operational efficiency while simultaneously improving risk visibility throughout products and processes via a consolidated risk management strategy. The unified suite of quality applications accelerates speed, boosts efficiency, and strengthens GxP compliance across all activities. Additionally, Vault QMS allows for the smooth implementation of essential quality management processes, incorporating built-in best practices for handling deviations, conducting internal and external audits, managing complaints, executing lab investigations, overseeing change control, addressing CAPA, and facilitating quality risk management, ultimately fostering a robust quality culture across the organization. By doing so, businesses can not only meet compliance requirements but also enhance their overall productivity and reputation in the industry.

Inova enhances the process of partnering in life sciences by guiding you through various stages of the lifecycle. Locating the ideal partner or opportunity can feel as challenging as searching for a needle in a haystack, requiring an exhaustive search through countless leads to discover the right information. Inova accelerates your ability to identify promising opportunities more swiftly. The journey from conducting due diligence to finalizing terms can be lengthy and complex, but Inova streamlines and simplifies crucial processes to save you precious time. After a deal is finalized, the pressure mounts to ensure it is both successful and profitable, and Inova equips you to start strong. Our cutting-edge digital partnering platform supports over 160 organizations in pharmaceuticals, biotechnology, and life sciences, enabling them to efficiently seek, negotiate, and collaborate. With our cloud-based solution, you can focus on what matters most: forging impactful partnerships and driving innovation.

ZAIDYN is a cutting-edge, cloud-based platform crafted by ZS aimed at transforming the life sciences sector. This innovative tool combines sophisticated analytics, machine learning capabilities, and smart workflows to help organizations streamline their processes in research and development, commercialization, and patient interaction. Designed with a modular approach, ZAIDYN offers scalable solutions that can be customized to meet diverse requirements, enabling smooth integration with current IT systems thanks to its open architecture. By delivering cohesive, high-quality data and insights, the platform fosters enhanced collaboration across different functions, which minimizes operational silos and encourages more informed decision-making. Prioritizing security and compliance, ZAIDYN upholds data privacy and meets regulatory standards, establishing itself as a trustworthy option for life sciences companies striving to innovate and elevate health outcomes. Ultimately, its comprehensive features provide organizations with the tools they need to navigate the complexities of the industry effectively.

ACE Essentials is the pre-validated Electronic Quality Management System Software (EQMS) designed for highly regulated industries. ACE Essentials includes 10 workflows, as well as all the required Standard Operating Procedures (SOPs) and Policies. This ensures that your quality management system is fully compliant from the start. ACE Essentials features include a complete audit trail that tracks every action within the system. This allows you to understand the risks associated assets. Features of ACE Essentials Pre-Configured Workflows Pre-Configured Event Management (Due dates, Scheduling, Reminders) - Pre-Configured Permission Based Security - Pre-Configured Full Documentation - 50+ documents - Multiple Site Capability - No Charge Upgrades for the Product's Life Pre-Configured Tasks Liste - No Validation Period Pre-Configured In System Notifications Pre-Configured Email Notifications

Introducing IDBS Polar, the pioneering BioPharma Lifecycle Management (BPLM) platform that streamlines tedious manual operations, empowering you to carry out processes more effectively while gathering the essential data needed to speed up market entry by addressing significant hurdles in process design, optimization, scale-up, and technology transfer. This innovative platform features interactive data analytics tools, including a bioreactor comparison tool tailored for biopharma development scientists. IDBS Polar excels at securely overseeing drug progression through comprehensive workflows, seamless integration, and insightful data analysis. Its structured workflows are crafted to ease the complexities of the BioPharma Lifecycle, ensuring process-aware planning, design, and execution of complete bioprocess and analytical unit operations. Meaningful integrations enhance the relevance of your data, while rapid incorporation into your development ecosystem fosters automation and establishes a robust, process-centric data framework. In an industry where precision and efficiency are paramount, IDBS Polar stands out as a vital solution for modern biopharmaceutical development.

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, ysura is based in Munich. It employs over 60 people from 17 countries. Ysura, an old Celtic word meaning Isar, is the name of the river that flows through Munich. It is a combination of ys (fast water) and ura(water). Ysura is short for fast water. Our products are fast and adaptable to the flow of information and tasks in the life sciences industry.

Ensuring that business processes are free of defects results in the creation of products without flaws. This is precisely why CASQ-it has been developed to cover every phase of your quality assurance and management procedures, beginning with the development stage and extending through material handling, all the way to support processes. The strength of CASQ-it is found in its process-oriented approach, offering a feature that allows your CAQ system to adjust seamlessly to your specific workflows rather than forcing your operations to conform to it. CASQ-it paves the way for your quality assurance efforts to advance into the future, enhancing quality and reliability, which in turn boosts customer satisfaction and lowers quality-related costs. Each CASQ-it module operates independently, allowing for the immediate optimization of distinct processes and workflows within your organization. Moreover, these modules can be combined in various ways, or utilized to form a holistic quality assurance framework tailored to your needs. Embracing this flexibility facilitates continuous improvement and fosters innovation within your quality management practices.

Sarjen offers QEdge, a powerful Quality Management Solution. This risk-based enterprise software for life sciences streamlines critical processes like Change Control, Deviation, CAPA, and Document Management. QEdge ensures full regulatory compliance (FDA, EU-GMP, ICH), driving operational excellence, data integrity, and audit-readiness in GxP environments, enhancing quality control and overall efficiency.

AmpleLogic's Quality Management Software, known as eQMS, is meticulously designed to fulfill the stringent demands of industries that face heavy regulation. This ISO 9001 certified cloud-based Quality Management System (QMS) is particularly suited for sectors such as Life Sciences, Food & Beverages (F&B), Cosmetics, Medical Devices, Gene Therapy, and similar fields. With the growing recognition of the difficulties tied to manual quality inspections—which can be both tedious and error-prone—more businesses are turning to QMS software solutions. These advanced systems significantly improve audit quality by automating processes, managing data effectively, and allowing for smooth API integration, ultimately fostering a more reliable quality assurance environment. This shift not only streamlines operations but also enhances compliance with industry standards.

Accelerate your launch process, enhance collaboration, and ensure everyone is unified with our innovative launch readiness software designed specifically for agile execution. Tailored for the pharmaceutical industry, this user-friendly SaaS solution is one that your whole organization will embrace and benefit from. Launches often lead to chaos, but SmartLaunch™ streamlines the process to ensure all team members are aligned, resulting in superior launch outcomes. With complete transparency over the entire launch initiative, you can eliminate delays caused by constantly chasing status updates, presentations, or spreadsheets. Avoid the pitfalls of fragmented systems by bringing together stakeholders from various teams, regions, and departments in a single platform. Foster collaboration across all functions and geographical locations to guarantee a seamless and effective launch. By automating repetitive tasks, you can save both time and resources, allowing you to concentrate on what truly matters—bringing your product to market. SmartLaunch™ keeps you and your team focused on the most critical tasks that require immediate attention, utilizing personalized task lists, notifications, Gantt charts, and adaptable Kanban boards to help you efficiently manage your priorities and workflows. This comprehensive approach ensures that your launch process is not only streamlined but also strategically aligned with your organization's goals.

Honeywell's TrackWise Digital® serves as an innovative cloud-based Quality Management System (QMS) aimed at enhancing the efficiency of quality and compliance processes within organizations. Drawing on nearly thirty years of expertise in the field, it features integrated modules that cater to various elements of quality management, such as document control, training oversight, and corrective and preventive actions (CAPA). The platform utilizes cutting-edge digital technologies, including artificial intelligence and machine learning, to deliver actionable insights in real-time, which fosters a proactive approach to quality management. Its adaptable, modular framework ensures smooth integration with current enterprise systems, allowing for quick deployment and growth. By optimizing quality processes and maintaining adherence to industry regulations, TrackWise Digital® enables organizations to accelerate product launches while effectively reducing risks. This comprehensive system not only enhances operational efficiency but also supports continuous improvement initiatives across the quality management spectrum.

The Life Sciences Cloud by Salesforce is an all-encompassing platform aimed at aiding pharmaceutical, biotech, and MedTech firms at every stage of the product lifecycle, from the initial clinical trials to the final commercialization phase. By leveraging AI-driven tools and insightful data, it enhances patient engagement, accelerates medical inquiry responses, optimizes clinical trial management, and boosts sales and marketing initiatives. The platform's features, including intelligent healthcare professional engagement, tailored patient services, and predictive analytics, enable organizations to create customized experiences, improve patient outcomes, and efficiently navigate complex regulatory environments. Additionally, its seamless integration with other Salesforce offerings and external tools ensures a comprehensive perspective of the healthcare landscape. This holistic approach facilitates collaboration and innovation among stakeholders within the healthcare industry.

Reshape Biotech offers an advanced automation platform powered by robotics and AI, specifically designed for microbiology labs, which revolutionizes traditional plate-based assays into scalable and data-rich workflows that can be replicated consistently. Among its key offerings are the innovative "Smart Incubator," a high-throughput imaging system, and a cloud-based "Discovery Platform," all of which automatically capture detailed images of Petri dishes and microtiter plates during their incubation periods, subsequently uploading this data to the cloud for immediate AI-driven analysis. The platform excels in accurately processing various readouts, including colony counting, radial growth, fluorescence, turbidity, color assays, seed-germination traits, and antagonistic assays, thereby eliminating the need for labor-intensive manual observations and minimizing human errors. In addition to enhancing efficiency, Reshape's solution creates a consolidated, searchable repository for all experiments and datasets, empowering teams to compare outcomes across different experiments, foster collaboration among various labs, and maintain consistency and reproducibility, irrespective of the scale of operations. This transformative approach not only streamlines workflow but also significantly elevates the quality of research outputs in microbiological studies.

Opvia empowers R&D, Manufacturing and Quality Management teams to build custom Process Operating Systems that streamline their workflows, giving them a competitive advantage. We work with startups and enterprises in a variety of industries including biotech, pharmaceuticals, food and beverage, engineering, and medical devices to digitize their processes. Our powerful tools and expert assistance give companies the freedom they need to create and deliver in a way that has never been possible before.

Close-Up International has been a trusted partner in the pharmaceutical industry for more than five decades, offering cutting-edge market data and analytic solutions across over 20 countries. Their comprehensive platform combines prescription data, retail and institutional market insights, and CRM/SFA tools to provide pharmaceutical companies with an integrated view of their markets. This enables better targeting of healthcare professionals, informed product positioning, and strategic decision-making during all product lifecycle stages, including pre-launch and post-launch. Close-Up’s technologies are deployed worldwide and are certified for quality and security standards, ensuring reliable and compliant data management. The company’s deep expertise supports clients in optimizing sales processes, managing regulatory complexities, and embracing digital transformations like AI-powered CRM for healthcare provider engagement. By delivering actionable insights and tailored consulting, Close-Up helps life sciences organizations maximize growth while controlling costs. Their solutions facilitate real-time market monitoring and foster collaboration between pharma companies and healthcare professionals. Close-Up’s commitment to innovation and data integrity makes it a strategic partner in the evolving healthcare landscape.

Ennov Quality Suite. A comprehensive QMS to increase efficiency and ensure compliance. Ennov Quality Suite Ennov Quality Suite combines the power of Ennov Doc and Ennov QMS with Ennov Report and Ennov Training to create an integrated quality management solution that improves operational efficiency and ensures compliance to industry standards like 21 CFR Part 11, GxP, and ISO. Ennov Quality offers a predefined inventory that includes quality documentation, processes, and workflows. These are based on industry standards and best practices. Ennov Quality customers can quickly get their system in production and begin to realize their return on investment. Ennov Quality, as all Ennov solutions, is easy to set up and requires no IT skills. A unified and intuitive content and information management platform that supports and enriches the entire Life Sciences product cycle. Our comprehensive QMS improves operational efficiency

Quality Collaboration By Design (QCBD) offers a comprehensive quality management software solution tailored for the manufacturing sector. This cost-effective, Windows-compatible application streamlines the process of obtaining and sustaining compliance with various quality management standards, including ISO 13485, ISO 9001, TS 16949, AS9100, and SQF 2000 / ISO 22000. Developed by CAMA Software, QCBD encompasses a wide range of modules that facilitate training management, supplier oversight, process deviation tracking, document control, equipment management, and additional functionalities. With its user-friendly interface, QCBD not only enhances operational efficiency but also ensures that businesses can easily adapt to evolving quality requirements.

ZipQuality offers a software-driven service designed to aid medical device manufacturers in launching innovative products. Our collaborative platform adeptly manages swift design modifications for agile teams while upholding regulatory standards. With a pre-configured system that incorporates processes and tools, there’s no necessity to modify your existing quality system. The integrated platform efficiently accommodates rapid design iterations for product documentation. Our team of seasoned consultants supports your team throughout the entire process. Built on the robust ENOVIA platform, our comprehensive, scalable software tools are tailored to meet your needs. This integrated solution allows for quick design adjustments while ensuring that product documentation and data remain synchronized and that all records are maintained in a state ready for audits. We cover essential areas such as product, hardware, and software requirements. Our expertise extends to the complexities of software-heavy medical devices. The ZipQuality framework is founded on a structured documentation approach that enhances systems engineering, promotes effective risk management, and ensures transparent traceability, making it an invaluable asset for any medical device company. Additionally, our commitment to continuous improvement means we regularly update our service offerings to align with industry advancements.

Paradigm 3 is a comprehensive platform available for both web and desktop use, tailored to assist businesses with compliance management focusing on Document Control, CAPA Compliance, and Competency Tracking and Training. This software provides a variety of features, including an event manager for handling incident investigations and customer complaints, email-delivered task notifications, and tools for preparing audits, among others. Industries such as Healthcare, Manufacturing, Test Labs, and Service Industries greatly benefit from the functionalities of Paradigm 3. With this innovative solution, organizations can eliminate the need for multiple additional modules to fulfill their compliance requirements. The system consists of four primary modules equipped with over 50 standard forms designed to address all aspects of Quality, Safety, and Environmental management. Furthermore, our form designer empowers users to create customized forms or modify existing ones, ensuring that every specific need is met seamlessly. This flexibility in form design enhances the platform's utility, making it an indispensable tool for businesses striving for compliance excellence.

A well-implemented Quality Management System (QMS) is essential for biotech firms to achieve regulatory compliance. It will also help them maintain product quality and safety. It will also help them manage risks effectively. It will drive operational efficiency. InstantGMP QMS was designed by quality and regulatory professionals for biotech companies. It is simple, affordable, and complete. It can be used by small-to mid-sized manufacturers in many different industries. This quality management software features guided workflows to reinforce adherence with government standards during the entire production process. It also has a variety of innovative features and specialized module. Maintain and improve the safety and quality of biotech products. Frameworks are provided for identifying, assessing and mitigating risk throughout the product's lifecycle to reduce the likelihood of quality incidents or product recalls.

BatchMaster Manufacturing ERP Solutions can be used by formula-based process manufacturers in the Food, Chemical, Nutraceutical, and Life Sciences industries. Our software supports batch production, formulation, packaging management, batch production, quality and recall, lot traceability & rappel, industry-specific compliance, planning, scheduling, mobile warehousing, and other process manufacturing functions. Manufacturers can use their existing financial systems to run our process manufacturing application, including QuickBooks, Sage 100&300 and Microsoft Dynamics GP. We offer an ERP solution for manufacturers looking to replace or upgrade existing business systems. It supports specific manufacturing, financials and sales as well as supply chain, purchasing and customer service. Our applications are available on-premise (purchased), and in the cloud (monthly subscription programs).

qmsWrapper is an interconnected Quality Management Software for startups and small businesses. It helps all companies that want to increase productivity with ISO 9001:2015 and MedDev creators to easily achieve and manage ISO 13485:2016 and 21 CFR 820. Best For 1. For companies who need guidance to implement and adopt validated QMS. 2. For companies who want to automate their quality management and go beyond a paper-based system.

You can now access your personal Quality Management Expert through an online platform designed for your convenience. With ready-to-use templates that can be seamlessly integrated into your organization, you can ensure efficient operations. Our offerings include comprehensive Quality Management Systems and digital solutions tailored for ISO 13485 related to Medical Devices, as well as ISO 9001 for General Quality Management, providing a robust framework for your quality assurance needs. Take advantage of our services to elevate your quality management practices to new heights.

Discover valuable insights within your data by utilizing the Cortellis™ suite of life science intelligence tools, enabling you to make more informed decisions throughout the entire R&D process. We have alleviated the burden of gathering, integrating, and analyzing data, allowing you to concentrate on the essential choices necessary for expediting your products' market entry. With a unique combination of extensive, high-quality data, fortified by profound domain knowledge, industry insight, and therapeutic expertise, Cortellis reveals crucial insights that facilitate data-driven decisions, ultimately speeding up innovation. Access tailored, actionable responses to your specific inquiries throughout the R&D lifecycle, drawing from the most comprehensive and in-depth intelligence sources available. By incorporating Cortellis into your daily routine, you can significantly enhance the pace of innovation and streamline your workflow. This makes Cortellis not just a tool, but a vital partner in your path to success.

Quality Link 7 is designed with a focus on both individuals and technology, leveraging our extensive experience and established platform to assist organizations in streamlining processes, reducing costs, and ensuring regulatory compliance through an intuitive business operating solution. By utilizing our document management module, Quality Link enhances efficiency and eliminates the need for cumbersome manual paperwork, allowing for seamless storage and management of every document generated. Users can conveniently print "uncontrolled" copies of documents and engage in a variety of document-related tasks directly within the module. This strategic organization significantly cuts down on clerical work performed by quality personnel by up to 90 percent. Our software also simplifies the transition by effortlessly converting documents from your former management system without any learning curve, while easily integrating with your preferred applications. With Quality Link, you can finally eliminate the burdensome task of manual document upkeep that often necessitates ongoing supervision, empowering your team to focus on more strategic initiatives. Additionally, the user-friendly interface ensures that all staff members can navigate the system with ease, further enhancing productivity across the board.

SoftExpert EQM stands out as an all-encompassing enterprise quality management software (EQMS) that aids organizations in obtaining and upholding ISO 9001 certification by automating and enhancing quality processes specifically designed for their unique products, operations, and business practices. This modular and adaptable platform integrates all essential quality initiatives, including process mapping and the management of documented information such as standard operating procedures, work instructions, and records, along with non-conformance reports, corrective and preventive actions, and quality indicators. Furthermore, the software efficiently oversees supplier relationships, addresses customer complaints, conducts quality audits, manages training and competencies, and evaluates quality risks and controls, as well as quality inspections and statistical process control, all of which contribute to a more agile and resilient quality management system. By streamlining these diverse functions, SoftExpert EQM empowers organizations to enhance their overall quality performance and compliance.

Platforce CRM, a cloud-based CRM that automates industry-specific business processes and improves customer engagement, is a closed-loop marketing and customer relationship management solution for pharmaceutical and life sciences companies. The system allows you to manage all aspects of marketing and sales activities, from the marketing cycle creation through territories assignment, databases creation, calls carrying, and KPI analysis.

PharmaWorx bridges the gap between marketing efforts and customer insights by providing immediate data collection and facilitating customer engagement, ultimately strengthening the customer relationship. Med Representatives utilizing PharmaWorx can seamlessly visit a physician's office, activate their iPad or Android tablet, and deliver product details while also completing prior assignments or jotting down notes from the current interaction, along with distributing samples. Should a physician show interest in specific media such as images, videos, or brochures, the representative can conveniently send this content directly from their tablet to the doctor’s email while still on-site. The adaptability of this solution allows for straightforward integration with various Enterprise Resource Planning or Supply Chain Management systems, ensuring prompt and relevant access to critical business data. By enhancing communication and responsiveness, PharmaWorx not only improves operational efficiency but also fosters a more informed and engaged healthcare environment.

Veeva Vault serves as a cloud-based enterprise content management solution designed specifically for the life sciences sector, effectively bridging content gaps within organizations to achieve global uniformity while still allowing for local autonomy. In the past, businesses were often required to use different applications for managing content and separate ones for handling related data. Veeva Vault distinguishes itself as the sole platform capable of integrating both content and data management seamlessly. This integration allows organizations to dismantle silos that exist at the system, site, and country levels, ultimately leading to more efficient workflows spanning commercial, medical, clinical, regulatory, quality, and safety functions. Furthermore, since all Vault applications utilize the same foundational platform, companies benefit from improved efficiency and compliance through a more cohesive document flow across various regions and departments. This ensures that content remains not only accessible but also up-to-date and relevant throughout the entire development and commercial life cycle, enhancing overall operational effectiveness. As a result, Veeva Vault empowers organizations to align their global strategies while still honoring local needs.