Scientist.com 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.

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.

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.

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.

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.

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.

Dexur aggregates claims data from multiple sources and coupled with innovative algorithms, we can show various insights to Life Sciences organizations including Sales and Marketing, Disease Burden Data, HEOR & RWE, Patient Journey, etc. Dexur utilizes its anonymized claims database to build disease burden data & dashboards at the national, regional, and hospital level. The outcomes for a specific disease (e.g., Diabetes, Chronic Kidney Disease) include the total cost of care, readmission, mortality, nursing home costs, length of stay, and any metric relevant to the disease. Dexur’s Life Sciences App Suite provides deep insights into various financial and clinical quality metrics that help in the analysis of Hospitals, Ambulatory Surgery Centers (ASC’s), Providers, and IDN’s. This helps life sciences companies have a more organised approach in targeting their products and services to most suitable clients.

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.

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.

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

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.

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.

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.

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.

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.

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.

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.

Maximize the impact of your scientific communication by selecting the best experts in the areas of excellence suited to your objectives. From common therapeutic areas to the rarest diseases, with Kolexia optimize your recruitment strategy for KOLs* in line with your objectives thanks to an intuitive interface and precise scientific and digital qualification of the identified profiles. Kolexia has a unique database, bringing together various information on health experts and their activities. This wealth of data allows an in-depth analysis of their profiles and their collaborations, as well as a better understanding of their impact in their field of expertise. Through this approach, we provide a comprehensive and up-to-date view from opinion leaders for an optimized medical strategy. *KOL : Key Opinion Leader

Veeva Medical CRM helps you develop strategic relationships and engage with key stakeholders across channels. Improve understanding of important accounts and ensure alignment among teams. Create meaningful interactions by planning, executing, and tracking engagement across channels. Scientific engagement planning, execution, and tracking. Integrated multichannel engagement with Veeva CRM Approved Email, Veeva CRM Engage and Veeva Digital Events. Coordinate planning and alignment with commercial counterparts. Built-in control and compliance, company-defined configuration, timeline view of activity between teams. Get a deeper understanding of scientific needs and interests with insights directly at the point of action. Easily communicate scientific content to drive high-value interactions. Access version-controlled and compliant content. Track and measure email and content performance.

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.

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.

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.

A secure platform for developing and sharing reproducible methods. Central and secure place to organize up-to-date/versionable methods with history and concurrent editing. Create and discover reproducible experimental and computational methods with video, reagents, detailed parameters, and more. Private & secure collaboration w/ HIPAA compliance, audit trail, approval/signature (21 CFR Part 11), 2-factor authentication, encryption, VPC, and more. A protocols.io Institutional Plan increases productivity, facilitates teaching, improves collaboration and recordkeeping, and accelerates progress across most research disciplines.

Stop wresting with cloud infrastructure and broken informatics tools. Start discovering biological insights today. Scientific discovery is bottlenecked by the fragmentation of tooling across biology and bioinformatics teams. We built a harmonized bioinformatics platform between wet lab and dry lab in the cloud to help teams accelerate their R&D. Import raw data from your cloud, your service provider, or your team's instruments. Develop and deploy custom bioinformatics workflows in any language. Stop wrestling with your infrastructure. Easily run any workflow and keep a log of every analysis. Ready-to-go interactive visualizations for NGS data with point-and-click plots. Latch supports integration with your organization’s AWS S3. Access hundreds of terabytes of data in an organic filesystem you are familiar with. Define bioinformatics workflows and dynamically generate no-code interfaces using Python with tunable compute and storage.

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.

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.

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.

Kea is a full service CRM solution for Pharma companies and Hospitals meeting APAC/Global needs. Kea is a comprehensive solution that enables sales and marketing teams to achieve higher levels of commercial excellence. Processes covered are Master Data Management, Closed Loop Marketing (CLM)/e-detailing, Sales Force Administration, Events and Continuing Medical Education (CME), Travel and Expenses automation, Coaching, and more. In the case of hospitals, Kea provides tracking of patient response to marketing activities. Users across the sales and marketing functions benefit from Kea. It is simple to use and yet empowers users with required analytics. Users dont have to access multiple applications. Their needs can be summarized in two pain points addressed in Kea: The users can analyze all "effort" KPI s in a "one-click" MIS dash board. They can also track "results" achieved. Kea is modular; some modules can complement Solutions like Veeva CRM and IQVIA

AmpleLogic Regulatory Information Tracker is built on the LOW CODE AND NO CODE (LCNC) PLATFORM and comprises two modules: ANDA and DMF Tracker. This Pharmaceutical RIMS Software can help you improve the quality of your data, boost operational efficiency, decrease mistakes, and streamline communication across departments.

Since its founding in 2021 from the Wyss Institute at Harvard University, Pluto has become a trusted partner of life sciences organizations around the country ranging from biotech start-ups to public biopharma companies. Our cloud-based platform gives scientists the ability to manage all of their data, run bioinformatics analyses, and create interactive and publication-quality visualizations. The platform is currently being used for a wide variety of biological applications, from preclinical / translational science research, to cell and gene therapies, drug discovery and development, to clinical research.

Working alongside both our in-house chemists and biologists, and our clients, we build products that deliver outstanding performance and scientific understanding. Chemaxon's product portfolio offers out-of-the-box solutions for scientists, back-end tools for IT professionals, components to add extra functionality, and integrations to make our technology available from 3rd party software like Microsoft Excel or KNIME. Trusted by over one million active users, Chemaxon is renowned for industry-leading software supporting scientific discovery with calculation, search and drawing tools. Our applications are widely used in life sciences R&D and education. We work with a variety of industries, counting most major pharmaceutical companies among our clients. Our offices are located in Budapest, Basel, Boston and San Diego, with distributors around the world.

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.

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.

Scispot is the best tech stack for biotech. It's the first-ever toolkit that lets you tailor it to your needs – no coding required. Think of it as a super combo of ELN + LIMS + Integrations + Analytics. You can set it up using a user-friendly interface (GUI) or by entering commands (CLI). It's about making your digital biotech dreams a reality. You can design your data infrastructure, automate your workflows and integrations and make your data ready for machine learning and artificial intelligence – all on one spot. Scispot even provides pre-made blueprints for major experiments, teamwork, and data management.

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.

BeeCTD is a full-featured eCTD management solution for pharmaceutical companies and regulatory agencies. Modular architecture and transparent licensing policy allow our users to choose from modules which they want to use – Reader, Compiler, Validator. Full-featured Reader which helps you to get an overview of the entire lifecycle of the dossier containing eCTD and/or NeeS sequences, including baseline submissions while transferring from NeeS to eCTD. Realtime, fast sequence validator fully compliant with eCTD / NeeS technical specification, incl. best practices criteria. The latest version of eCTD validation criteria is always updated, older versions are available. Get your documents compiled into the eCTD-compliant format. Use our eCTD compiler tool as a product, which allows you to compile yourself or as a service - we compile for you on demand.

ysura conceives and develops innovative Sales and Marketing Solutions for the Pharmaceutical Industry and offers them as a Software-as-a-Service. Founded in 2012 and based in Munich, ysura has together with the sister company MuniConS over 60 employees from 17 different countries. All of ysura’s shares are still held by the founders and the employees. With our state-of-the-art mobile Pharma-CRM Solution and MuniConS’ consulting expertise, we assist Pharma companies in their successful digital transformation. ysura is the old Celtic word for Isar, the river that flows through Munich. It comes from ys (fast) and ura (water). Ysura means fast water. A perfect description for our products: fast and perfectly adapted to the flow of tasks and information for the life sciences industry.

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.

Powerful data search tools allows quick access of the data. An innovative and easy-to-use calendar is a great help for medical representatives in arranging their appointments. Various report generation and data analysis tools provide the possibility to dissect different sections of representatives’ work. Additional time dimension allows analyzing changes in dynamics of customer characteristics as well as a target setting for different time periods. Online. The application connects to central database directly. Offline. User can use the application offline without any limitations and synchronize the data when the internet connection is available. PharmaCODE is the newest customer relationship management (CRM) solution provided by SoftDent for pharmaceutical representative companies. This application was created combining newest technologies and all the experience that we have gathered during nine years developing, supporting and maintaining Customer Profiling.

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.

Our Sales Force Automation enables pharmaceutical companies in being ahead of the changing market dynamics. It is a robust way to effectively pursue and achieve its business objectives. The key competencies of field force can be assessed for better performance. Our SFE allows the Sales team to target, prioritise, assess physician needs and develop solutions around those needs. Our analysis transforms the filed force into a customer-focused field organisation. Reporting made simple and on-the-go for the field force to spend more time on promoting the product. SANeFORCE.com provides SFE Product accessible through Web and Mobile. Field Fore can submit their Tour Plan, Daily Activity, Internal Email, RCPA Analysis to the corporate office Through Mobile App Itself. This is to make the field force more effective and quality time with Customer and instant information about the business.

A science-aware™ data integration solution made for modern science. The data-driven future of discovery can’t be built upon the broken data and legacy architectures of the past. As the volume and variety of research data continues to exponentially grow, siloed approaches to data management and analysis become even more untenable. And yet, for most organizations, this information still resides across a myriad of systems. If this data has been brought together, it is often done through a separate SDMS or business intelligence tool that fails to embrace the central and highly integrated role of truly scientific analysis. A science-aware™ data integration solution made for modern science, Jarvis connects and harmonizes your collective scientific intelligence, including your instrument and application data, so that you can realize the fullness of its value. This streamlined insight is made readily available to scientists in a living knowledge graph that is highly searchable.

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!

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.

The unique XetaBase platform simplifies tertiary analysis, aggregating, indexing, and enriching secondary genomic data, enabling continual re-interpretation to unlock research and clinical insight. XetaBase accelerates data management and the cost-effective application of genomic data in the lab and clinic. XetaBase encompasses genomic scale, the greater the volume and complexity, the greater the insight and outcomes. XetaBase is a genomic-native technology, built on the open-source, OpenCB software platform to meet the scale, speed, and re-interpretation demands of genomic medicine. Zetta Genomics delivers genomic data management fit for the precision medicine age. XetaBase is a completely novel solution to the challenges of genomic data. It sweeps away obsolete flat file approaches to bring meaningful and actionable genomic data into the lab and the clinic. XetaBase empowers continual re-interpretation while scaling seamlessly as databases grow to encompass genome sequences.

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!

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.

TikaMSL is a business intelligence, CRM and advanced analytics tool designed specifically for MSLs. It allows Medical Science Liaisons to gain deep insights about the industry and stay informed by connecting with multiple third-party sources. It enables them to be very strategic with their KOL interactions and share the vital information they collect over the course of time with the rest of their organization in a fully compliant manner.

Empowering pharma companies and CDMOs to scale manufacturing while addressing supply chain bottlenecks, complex raw materials, and increasing development costs. Leverage the predictive power of AI and machine learning with the industry's leading manufacturing cloud. Always in a compliant manner. Collect and integrate real-time and historical data in a GxP-compliant manner from multiple sources, turning it into actionable insights. Leverage artificial intelligence (AI) and machine learning to find patterns that may lead to deviations and fix them before they become problems. The Aizon platform uses real real-time data capture from disparate data sources and predictive models to optimize pharma manufacturing processes. The Aizon platform performs GxP-compliant data acquisition, storage, and consumption making audits easier. Aizon works with international regulatory bodies to make sure AI algorithms can be qualified.