Aclid Alternatives

SciNote is a cloud-based electronic lab notebook (ELN) with built-in inventory, compliance, & team management tools. It is trusted by the FDA, USDA, European Commission, and 100K+ scientists in over 100 countries. Each premium plan comes with top-rated customer support, and a customer success manager who will work closely with you to ensure successful onboarding and implementation. SciNote provides a top-rated set of data management functionalities, such as inventory tracking & management, protocol & SOP management, compliance (CFR 21 part 11 & GxP), team management & collaboration, integrations and API, project management, safety & security of data and more. SciNote is based in Middleton, WI, USA, with offices in Europe.

Complete EHSQ solution designed for manufacturing, utility and government organizations that allows plant managers to track, analyze and report on their EHSQ processes. Our solution automates workflows, centralizes data and simplifies collaboration. TenForce offers various integrated modules to help streamline processes such as Audits, Incident Management, Lockout/Tagout (LOTO), Permit to Work, Management of Change, and Shift Management. It offers mobile capabilities, which allow field workers and inspectors to access the software on mobile devices. Its built-in data analytics and reporting functionality enables managers to gain insights into the processes and risks of their industrial plants or public infrastructure assets. This visibility helps them address environmental, health, safety, quality, and compliance issues. TenForce helps manufacturers optimize their established processes while minimizing incidents.

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

The modern, flexible, easy-to-use LIMS. QBench enables our customers to get a LIMS up and running faster. Automate your entire lab with our developer-friendly API, Inventory Management, Customer Portal, Billing, and Quality Management System modules. QBench is a cloud-based Laboratory Information Management System (LIMS) that enables labs to streamline their entire testing workflow, from sample receiving to automated results reporting. 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. View hundreds of PDF reports/COAs before publishing or emailing. Generate barcodes and create labels that you can customize for your samples. See counts and latencies for different data types in QBench. This includes metrics like turnaround time, sample counts per test, sample delay, and more!

Eliminate the delays and administrative burdens of contracting, qualifying, and setting up new suppliers. Instead, just instantly order what you need from our qualified network of 3,500+ suppliers – all under a single contract. From the moment a project begins, we help you automate each task into one simple-to-use process, streamlining request-to-pay workflows, stakeholder collaboration, and milestone management. And our dynamic workflows can be customized to work with your unique purchasing practices. We simplify the complexities of payment processing and equip you with robust analytics and reporting tools to track and analyze your spending. It's easy to create custom reports that reflect your priorities. And live dashboards help your teams collaborate, make data-driven decisions, and take real-time action.

Pepper Flow’s unique features are built specifically to help life science companies streamline how marketing, medical, legal, and regulatory professionals work together. As a marketer, you need tools that allow you to move fast and keep things simple during advertising and promotional reviews. Get your critical campaigns and content to market to support your organization’s strategic initiatives. Maximize productivity by collaborating in real time to address feedback and turn around revisions. Spend less time managing the review process and more time on your high-priority to-dos. Pepper Flow is cloud-based, enterprise-grade software that enables life science companies to improve their competitive advantage, market products with efficiency, and maintain rigorous compliance. You need to move fast in order to deliver content to your key audiences. Pepper Flow’s intuitive interface allows you to get work done quickly and effectively.

Enterprise Quality Management Software in the cloud for the life sciences. In today’s complex operational environment, technology plays a vital role in ensuring that QA is made aware of the issues as they happen. Gaining insight into the performance of your quality management system and the current state of your operation helps you to be more proactive, which minimizes risk and eliminates costly delays. Montrium has designed its Enterprise Quality Management system (EQMS) to enable life science companies to tackle the quality challenges that they face in content management head-on. All of our SharePoint QMS modules can be used independently or together as a fully integrated quality management system. These modules are available as part of our Montrium Connect Platform and can be deployed on-premise or in the cloud. Perfect for pharmaceutical companies, contract manufacturing organizations, medical device companies. Built to achieve compliance with GMP and GCP requirements.

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.

ActivityBase is the established industry software platform for screening data management, with feature-rich data analysis tools, built-in object/compound registration tools and the industry standard database. ActivityBase provides analysis support for a wide range of biochemical, cellular and biophysical assay formats (including Ion Channel, FLIPR, Kinetic, SPR, Mass Spectrometry assays). The system integrates into HCS imaging stores (Perkin Elmer Columbus, Thermo Fisher HCS Studio, Molecular Devices MDCStore) for easy import of data and images. ActivityBase also features built-in compound registration and plate management tools. With ActivityBase, you can easily track and manage the results from years of assays in one system. The system can be configured to meet your needs, without having to buy new analysis packs, and, through improvements in your data analysis processes, can even increase your lab analysis tenfold.

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.

Ideagen PleaseReview is a document review, co-authoring and redaction software application that helps you to control and manage all aspects of the document creation and review process, delivering: Improved operational performance, productivity and efficiency, Stronger compliance and business oversight. Mitigation of regulatory, legal and commercial risk. PleaseReview is our document collaboration software, designed to make your collaborative process easier, safer and more efficient. Wherever you are working, and whether you’re collaborating with colleagues or third parties, PleaseReview provides a secure, controlled environment for real-time document review, co-authoring and redaction. So you can protect sensitive information and focus on delivering high-quality documents.

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.

MDprospects is a web-based software tool designed for medical practices to manage leads, maximize patient conversion rates and increase revenues. Know where your leads are coming from and automatically capture online inquiries and walk-ins. Plus, our OD CRM increases patient generation by managing referrals. MDprospects makes it easy to communicate and nurture leads with its email marketing feature, task management system, 2-way text messaging and online scheduling. Track your efficiency and take the guesswork out of follow-up. See your conversion rates grow with automated task management, informative email blasts, and lead nurturing drip campaigns. Appointment scheduling is a simple way to have people come to you and get them into your practice. By filling out a simple-to-use form that feeds directly into your database of leads, appointment scheduling makes it effortless for a person to become your patient and book a consultation at your practice.

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

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.

In today’s ever-changing regulatory landscape, Titanium offers a comprehensive suite of applications designed to keep your sample management program compliant, efficient, and streamlined. Experience the unparalleled benefits of our cloud-based, SaaS platform that brings together cutting-edge solutions tailored to comply with PDMA and 21 CFR Part 11. Titanium offers a dynamic suite of applications designed to address specific compliance challenges while seamlessly inter-operating, providing an integrated and comprehensive solution for all your compliance needs. Titanium is built to grow with your business, ensuring that each data point exists only once and is accessible across all applications. Maintain transparency and accountability with built-in audit trails for seamless tracking and reporting. As a mature application, Titanium consistently evolves through regular upgrades, keeping you at the forefront of compliance technology.

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.

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.

Only SAS delivers a single, open, cloud-native statistical computing environment for clinical research with embedded analytic tools, support for data standards, and optional integrated analytic applications. Our analytic foundation for clinical research helps you modernize and deliver new therapies to market faster to improve health. Manage and analyze information in a collaborative platform, streamline processes, and more efficiently deliver trial results to regulatory authorities. Provides a cloud-native, single solution for clinical analysis and submission with everything you need for validation, regulatory compliance, versioning, audit trails, and documentation support. Allows for automation through workflows, support for current and future integrations, and implements and properly manages data standards and controlled terminology. Includes central hub for all incoming data, automated data quality analysis, better data management, and analytical data preparation.

Get your sales reps to see more physicians through Ammras organizer. An effective sales representative call means showing the right materials, at the right time. That's it, Ammras is a tool that helps your representative to do that. It equips life science companies with the decision support tool which analyzes real-time market data, channel activity and HCP (Healthcare professionals) with preference to provide life science companies with insights, clarity, and guidance to deliver the right information at the right time. It makes use of data, extracting only what’s relevant and valuable at the time of the decision-making process and present it before you and your field force. We focus on simplicity and usability thus make team focus on selling by the effective utilization of time to build up a strong relationship with HCP, in order to generate more revenue.

SmartContent enables marketing teams to effectively engage with healthcare professionals, through a seamless and personalized experience. You don’t need any more certified digital agencies to create your own content! Take back control of your marketing tools and expenses. With SmartContent, marketing teams can easily manage all marketing materials such as visual aids, dedicated microsites, or polls. Make available to your reps the right content automatically according to the profile of each HCP, while ensuring compliance rules for your content. Marketing teams can capture instant insights from call sessions, allowing you to refine and improve for greater market success. Interact with healthcare professionals through different digital channels, for a seamless and personalized omnichannel experience. In just a few minutes, create your marketing templates without the need to code, segment your database, create workflows to get the best impact, and analyze campaign KPIs.

DNAnexus Titan™ powers the future of genomics research and clinical pipelines with trusted, high-performance data analysis solutions. Legacy informatics tools were not designed to manage today's higher volumes of sequencing data. With home-grown, do-it-yourself systems, research centers and clinical diagnostic testing companies are finding it difficult and time-consuming to create, refine, validate, and execute pipelines at scale. DNAnexus Titan™ removes bottlenecks in development and production with a unified platform that brings all your data and pipelines together in one place and delivers unparalleled efficiencies. Leave the heavy lifting of managing industry and region-specific security and compliance requirements to us, while meeting the growing global demand for sequencing data.

Built-in digital asset management for life sciences enables global reuse and reduces spend on promotional materials. Marketing teams can easily publish and withdraw content to digital channels and ensure only approved assets are in use. Accelerate content approval and time to market with industry-leading medical, legal, and regulatory (MLR). Built-in claims library with reference links reduces the administrative burden and risk of managing claims across countries, channels, and assets. Our industry cloud solutions provide data, software, services and an extensive ecosystem of partners to support your most critical functions from R&D through commercial. Veeva helps companies of all sizes bring products to market faster and more efficiently and maintain compliance.

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.

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.

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

Model N delivers an end-to-end platform empowering companies to maximize revenue as they transform Sales, Marketing, Channels, Finance, and Legal processes. Model N’s revenue management solutions help you maximize revenue by transforming siloed, tactical activities into strategic end-to-end revenue processes through automation and intelligence. Revenue Cloud bridges the gap between front-office and back-office activities providing a unified system of record for all revenue execution. Model N allows customers to easily configure and quote complex products, quickly come to terms on complicated contracts, have more accurate and timely channel data ensuring visibility into channels, and efficiently manage incentive programs avoiding overpayments. Model N Rebate Management helps you better engage your channels to improve and optimize revenue.

EvolveICM is the incentive compensation management module of our SPM software built for insurance companies. This solution is built to help carriers automate commission calculations, saving the time and resources involved with completing this task manually. You can take control of the performance of your sales channels while automating processes, establishing incentive programs and more. EvolveICM is made for insurance carriers and agencies that use complex commission calculations, such as those in health insurance and Medicare industries, with core, flat, percentage or split commissions. Our commissions management software computes these payouts for you. While manual calculation can take hours, our automated process takes less than 10 minutes, even with eight-figure payments.

Clustermarket is the world-leading lab management system helping all types of laboratories optimize their operations and accelerate results. Clustermarket equips research teams with an easy-to-use software solution which enables them to coordinate equipment usage, plan maintenance activities, and generate reports and forecasts for resource planning. The intuitive system is designed for fast implementation and high adoption within the organization, whilst also offering integrations to various other software solutions such as ELNs and asset monitoring. Feature summary: - Equipment scheduling and maintenance - Reports & analytics - Asset monitoring via sensors from our partners - Integrations with ELNs and other systems Optimize your labs' processes and improve equipment utilization now!

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

AiDEA is the evolution of Customer Relationship Management (CRM) where Artificial Intelligence is the foundation and the engine behind operational and analytical solutions powered by Microsoft Dynamics 365®. Its native ability to integrate data from multiple sources offers a 360° view of the customer, facilitating the implementation of a true omnichannel strategy, and providing proactive contextual information and insights to the teams involved. An innovative solution able to support company-wide activities with an easy adoption process is the way to success. Thanks to Intelligent Insights, AiDEA allows access to the right information at the right time, to make the best decisions. The solution is cross and multi-device and can be used simultaneously on multiple devices. This makes data and information-sharing fluid, immediate, and up-to-date in real-time. Optimize the planning of your marketing activities by means of strategic suggestions designed to help you achieve your objectives.

With its comprehensive suite of integrated software, StarDrop™ delivers best-in-class in silico technologies within a highly visual and user-friendly interface. StarDrop™ enables a seamless flow from the latest data through predictive modeling to decision-making regarding the next round of synthesis and research, improving the speed, efficiency, and productivity of the discovery process. Successful compounds require a balance of many different properties. StarDrop™ guides you through this multi-parameter optimization challenge to target compounds with the best chance of success, saving you time and resources by enabling you to synthesize and test fewer compounds.

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.

The life sciences industry is one of the most complex in the world. These companies need a responsive IT infrastructure with the ability to control compliance costs. Improving business performance as you work to bring new products to market in a timely manner is critical. The explosion in the need for research, development, and regulatory compliance is driving the demand for a more flexible operating environment. Nothing is more critical than access to real-time information on production processes and business operations. Life science companies depend on this data to make sound business decisions, maintain compliance, and run efficiently. Time-to-market and profitability pressures are intense. Many times, being the first company to market and patent a new product is a key indicator of potential success. Often these needs are balanced against demand for manufacturing existing products.

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.

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.

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.

TikaMobile’s National Account Manager solution enhances the strategic planning and execution capabilities across various teams. TikaNAM helps managers optimize team efficiency by providing them with access to individual IDN and GPO performance by hospitals, units, revenue, compliance, and more. With all of this intelligence, national account managers are able to segment IDNs, create a strategic plan, generate proposals, analyze how each product group is doing and track the performance of the IDN itself across geographies. On this easy-to-use platform, users can quickly generate what-if pricing scenarios on individual products, as well as product bundles, and instantly share these pricing proposals with their teams. This allows national account teams to respond instantly to pricing queries from the field, addressing a long-standing problem faced by the industry.

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.

From the perspective of cell production management, most enterprises hope to control all factors surrounding production, such as sample collection, raw and auxiliary materials, instruments and equipment, personnel, environment and process, so that they can make efficient use of resources. Therefore, there is no shortage and redundancy of resources, but production quality can be guaranteed. In addition to the above problem management, bio cellmes also provides product tracking and production process management (including SOP) In the system, from pre job preparation, production process, to completion clearance), QC (product quality inspection, reagent quality inspection, etc.), QA (environmental control, deviation handling, finished product release audit), etc.

Nextflow Tower is an intuitive centralized command post that enables large-scale collaborative data analysis. With Tower, users can easily launch, manage, and monitor scalable Nextflow data analysis pipelines and compute environments on-premises or on most clouds. Researchers can focus on the science that matters rather than worrying about infrastructure engineering. Compliance is simplified with predictable, auditable pipeline execution and the ability to reliably reproduce results obtained with specific data sets and pipeline versions on demand. Nextflow Tower is developed and supported by Seqera Labs, the creators and maintainers of the open-source Nextflow project. This means that users get high-quality support directly from the source. Unlike third-party frameworks that incorporate Nextflow, Tower is deeply integrated and can help users benefit from Nextflow's complete set of capabilities.

PRxCloud is a revolutionary cloud-based sales and marketing automation software for Pharmaceutical Marketing & Distribution companies. It is designed to simplify marketing, sales, and daily operations and to empower medical representatives by helping them plan better and maximize sales. Native IOS and Android Mobile App, designed with the philosophy “Focus Right! Work Smart!!”, is extremely user-friendly and convenient. The App has offline capabilities which ensures that there is no interruption during work. It improves productivity of field force by leveraging easy-to-use features such as daily activity reporting, tour planning, assigning targets, expense management, order booking, e-detailing, gift/sample management, RCPA competitive analysis and GPS tracking. Our customers can choose to subscribe PRxCloud in SaaS model or opt for an enterprise license. For enterprise licensing we do offer option of private hosting or in house hosting.

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!

ODAIA's MAPTUAL looks at the customer journey end to end. Using cutting-edge analytical tools, AI and ML, MAPTUAL delivers predictive insights to pharma commercial teams on a real-time basis enabling precision targeting, better resource utilization and commercial agility. All this in one software as a service (SaaS) package that works with the data you already buy. A customer insights tool that integrates the data you already have from across internal and external sources. MAPTUAL applies unique and proprietary algorithms to deliver real-time, predictive insights to your sales and marketing teams so they can deploy their resources more efficiently and create hyper-personalized customer engagement. Refine customer targeting using market drivers. Adjust them in real-time as necessary. Measure, optimize and hyper-personalize the right message to the right HCP using the next best channels in order to deliver the next best experience.

Organizational business complexity is rising. The lifetime of apps is decreasing. Address the business issue, collect data, and discard the solution once the issue has been resolved. Low Code No Code (LCNC) Application Development Platforms enable this in today’s environment. The AmpleLogic Low-Code and No-Code (LCNC) Development Platform includes a drag-and-drop form designer. It is a workflow that connects the people and processes within your organization to those outside of it. With the assistance of a LCNC Platform such as AmpleLogic, you may more effectively handle your organization’s particular requirements and close gaps across your business processes.

AmpleLogic's Quality Management Software (eQMS) is intricately crafted to meet the rigorous requirements of heavily regulated industries. The ISO 9001 certified cloud-based Quality Management System (QMS) is ideal for Lifesciences, Food & Beverages (F&B), Cosmetics, Medical Devices, Gene Therapy, and analogous sectors. As businesses acknowledge the challenges associated with manual quality checks—prone to both laborious efforts and errors—they are increasingly adopting QMS software solutions. These systems play a pivotal role in enhancing audit quality through process automation, efficient data management, and seamless API integration.

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

Metacoder makes processing data faster and easier. Metacoder gives analysts needed flexibility and tools to facilitate data analysis. Data preparation steps such as cleaning are managed reducing the manual inspection time required before you are up and running. Compared to alternatives, is in good company. Metacoder beats similar companies on price and our management is proactively developing based on our customers' valuable feedback. Metacoder is used primarily to assist predictive analytics professionals in their job. We offer interfaces for database integrations, data cleaning, preprocessing, modeling, and display/interpretation of results. We help organizations distribute their work transparently by enabling model sharing, and we make management of the machine learning pipeline easy to make tweaks. Soon we will be including code free solutions for image, audio, video, and biomedical data.

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

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.