Titanium 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.

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!

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.

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.

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.

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.

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.

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.

Our immune system drives our most important biological processes. It protects us from sickness and disease by defending against outside invaders like pathogens and keeping our internal systems in equilibrium. No two of us share exactly the same immune makeup, and each of our systems is constantly evolving. Mapping and studying this complexity in great detail unlock the insights that accelerate research and derive better therapies for all. For too long, single-cell data analysis has lagged behind the technology that generates these data. That’s because the standard manual workflows, limited in resolution and speed, only allow for a small amount of cellular information to be seen. Advances in medicine are driving us more and more toward highly targeted treatments, with many therapies at the forefront being constructed from the patient’s own immune cells. Our AI-driven computational analysis technology unlocks insights to discover therapies and advance their development.

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.

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.

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.

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.

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.

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.

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.

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.

RegDocs Connect gives your operational and regulatory teams the tools they need to prepare complete and compliant submission ready documents and records. Built with the end user in mind, collaboration, automation and quality are the foundation of this solution. Automated workflows manage your records lifecycle from draft to final, enabling your team to be in complete control of your regulatory documents at all times. Mapping of document types to the EDM reference model and eCTD facilitates organization and retrieval of documents for inclusion in regulatory submissions. Proprietary tools such as PDF/A Publishing, document classification, and unique document identifiers provide a powerful regulatory document management solution that pulls information from across your organization, into one manageable solution. With the rise of electronic submissions to regulatory agencies and the increased complexity of drug development, the ability to produce submission-ready, quality content

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.

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.

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.

DF mSafety AI is a cloud-based safety platform that uses the power of AI/ML and automation to deliver efficiencies and a great user experience in Safety Case Management and Signal Detection for Drugs, Cosmetics, Vaccines, Neutraceutical and Medical Devices. DF mSafety AI is built on Datafoundry’s Integrated Cloud Platform - DF Safety 4.0 which supports scalable and secure AI/ML driven Safety Case and Signal Management, pre-built connectors to enterprise systems, adhere to regulatory requirements and industry standards.

PharmaWorx helps to close the loop between marketing activities and customer feedback by offering real-time data capture and customer responsiveness, thus enhancing the overall relationship with the customer. Med Reps that use PharmaWorx can make a planned or informal visit to a doctor's office, instantly switch on their iPad or Android tablet and present product information to the doctor along with completing previously recorded tasks or capturing notes for the current visit, as well as drop off samples. If a doctor is interested in a particular image, video or brochure, the med rep can mail the content directly from the iPad to the doctor's email while still at the doctor's office.The solution is flexible and can be easily integrated into any Enterprise Resource Planning or Supply Chain Management solution for immediate and up-to-date access to business information.

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.

ProSellus makes finding new customers fast and easy. Search for new customers that fit your profile by using data points that are meaningful to you. Easily search for customers by name, specialization, procedures, drugs, and geography. Field Sales Reps need two things in a sales tool: simple and useful. Traditional CRMs & Sales Enablement Tools are not simple, and they definitely do NOT help drive revenue for the always-on-the-go healthcare sales rep. ProSellus is different. Designed by a team of top producers in medical device sales, this mobile sales tool gives your sales reps unparalleled insight into all the relationship and revenue opportunities in their territory ON TOP of all the important features of a CRM. Help your sales reps focus on the right physicians, at the right time, to create new opportunities, using data we have built into the tool or that you already own (or both!).

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

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.

Our platforms are built on the technology stack of Microsoft to quickly integrate into the systems and tools you already use. Our solutions provide a true 360° view of all customers and the omnichannel journeys needed to orchestrate their operations, delivering unrivaled value and future-proofing an organization in a dynamically changing digital world. Exeevo provides a single subscription model for the entire platform, workloads, and apps. There are no additional or hidden costs making for an attractive total cost of operation. Exeevo is built on the Microsoft technology stack making it familiar and easy to deploy, configure, customize, enhance, and upgrade. Exeevo is committed to our customer's success. We own implementation and adoption, to ensure a successful deployment. Through our teams and industry partners, we deliver the value our subscribers need. We provide can training, retraining, change management, and communications throughout the lifecycle.

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.

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.

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

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.

SmartTeam enables sales & operation managers to monitor and enhance teams' performance. Implement data-driven strategies and transform your data into actionable insights! We have built the whole software suite with life sciences managers. Manage your sales and distribution channels effectively, enhancing sales teams’ performance and improving business results significantly. SmartTeam allows managers to monitor business conditions, products, and deliveries from a flexible and complete administration interface. SmartTeam provides access to your sales and operation managers to real-time information from the field. Benefit from a powerful Business Intelligence tool that allows you to track all relevant KPIs for your commercial performance. Using Euris solutions, sales, and operation managers can quickly create, update, share, and analyze e-learning content. E-learning can be synced to product launches and can be used to train medical representatives to meet the needs of the market.

Harness the power of biomedical data with Polly. The Polly Platform helps to scale batch jobs, workflows, coding environments and visualization applications. Polly allows resource pooling and provides optimal resource allocation based on your usage requirements and makes use of spot instances whenever possible. All this leads to optimization, efficiency, faster response time and lower costs for the resources. Get access to a dashboard to monitor resource usage and cost real time and minimize overhead of resource management by your IT team. Version control is integral to Polly’s infrastructure. Polly ensures version control for your workflows and analyses through a combination of dockers and interactive notebooks. We have built a mechanism that allows the data, code and the environment co-exist. This coupled with data storage on the cloud and the ability to share projects ensures reproducibility of every analysis you perform.

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.

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.

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.

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.

The Phyzii platform consists of various products created specially for the pharma sales force with specific goals in mind. These feature rich products have the common indigenous scalable and flexible Phyzii CRM base on which these modules are created and integrated. Phyzii has been created and enriched since 2007 by the whole pharma ecosystem consisting of clients, users and our internal product team. It is offered on the cloud in various financial models. Phyzii platform supports the following verticals. Comprehensive implementation services from the scoping and mapping to finally going live and hyper care. Experienced product specialists carry out training of trainers and/or end users for operation and troubleshooting of the Phyzii Platform. Post implementation lifelong support for all types of issues and requests from client operations team by email or phone.

Inception CRM is a robust and user-friendly CRM solution for primary and specialty care as well as retail pharmacy life science field sales teams. A GDPR-compliant solution, Inception CRM is fully adapted to the needs of European life science organizations. It offers end-to-end support to reps in the field, helping them plan, execute and optimize their sales campaigns. Inception CRM guides users through their daily tasks, while providing valuable insight into their customers, territories and opportunities. Inception CRM’s powerful search helps sales reps quickly find the right customers, while detailed customer cards tell them everything they need to know. Inception’s intelligent workflow-based planner keeps field sales reps productively focused on the right tasks so that every sales campaign is a success.

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.

Titanium is a next generation, comprehensive, client - oriented, new business policy admin system driving digital change, built for ease of implementation, all while minimizing risk. Offering life insurance carriers access to 1000's of configurable products out of the box. ​ Launch individual, group, fixed, variable, traditional and non-traditional life, health, and annuity products in weeks. Titanium is a true end-to-end platform with over 42 years of success. LIDP has a 100% success rate in implementation and conversion projects. The company is privately held allowing for the focus to be strictly on the customer and building the best solutions for their needs while taking advantage of the most modern technology available. Thus futureproofing carriers core solution for years to come.

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.

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.

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.

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.

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.